NEW
Try the new Transcript table
These reference sequences exist independently of genome builds. Explain
These reference sequences are curated independently of the genome
annotation cycle, so their versions may not match the RefSeq versions in the current
genome build. Identify version mismatches by comparing the version of the RefSeq in
this section to the one reported in Genomic regions,
transcripts, and products above.
mRNA and Protein(s)
-
NM_001166381.2 → NP_001159853.1 DNA repair protein RAD52 homolog isoform 1
See identical proteins and their annotated locations for NP_001159853.1
Status: VALIDATED
- Description
- Transcript Variant: This variant (1) encodes the longest isoform (1).
- Source sequence(s)
-
AC117667
- Consensus CDS
-
CCDS51887.1
- UniProtKB/Swiss-Prot
-
P43352
- Related
- ENSMUSP00000125502.2, ENSMUST00000162461.7
- Conserved Domains (1) summary
-
- TIGR00607
Location:39 → 200
- rad52; recombination protein rad52
-
NM_001166382.2 → NP_001159854.1 DNA repair protein RAD52 homolog isoform 3
Status: VALIDATED
- Description
- Transcript Variant: This variant (3) uses an alternate in-frame splice site in the 3' coding region, compared to variant 1. This results in a shorter protein (isoform 3), compared to isoform 1.
- Source sequence(s)
-
AC117667
- Conserved Domains (1) summary
-
- TIGR00607
Location:39 → 200
- rad52; recombination protein rad52
-
NM_001410284.1 → NP_001397213.1 DNA repair protein RAD52 homolog isoform 5
Status: VALIDATED
- Source sequence(s)
-
AC117667
-
NM_001410285.1 → NP_001397214.1 DNA repair protein RAD52 homolog isoform 6
Status: VALIDATED
- Source sequence(s)
-
AC117667
-
NM_001410286.1 → NP_001397215.1 DNA repair protein RAD52 homolog isoform 7
Status: VALIDATED
- Source sequence(s)
-
AC117667
-
NM_001410287.1 → NP_001397216.1 DNA repair protein RAD52 homolog isoform 8
Status: VALIDATED
- Source sequence(s)
-
AC117667
-
NM_001410288.1 → NP_001397217.1 DNA repair protein RAD52 homolog isoform 9
Status: VALIDATED
- Source sequence(s)
-
AC117667
-
NM_001410289.1 → NP_001397218.1 DNA repair protein RAD52 homolog isoform 10
Status: VALIDATED
- Source sequence(s)
-
AC117667
-
NM_001410290.1 → NP_001397219.1 DNA repair protein RAD52 homolog isoform 11
Status: VALIDATED
- Source sequence(s)
-
AC117667
-
NM_011236.3 → NP_035366.2 DNA repair protein RAD52 homolog isoform 4
See identical proteins and their annotated locations for NP_035366.2
Status: VALIDATED
- Description
- Transcript Variant: This variant (4) uses an alternate in-frame splice site in the 3' coding region, compared to variant 1. This results in a shorter protein (isoform 4), compared to isoform 1.
- Source sequence(s)
-
AC117667
- Consensus CDS
-
CCDS20477.1
- UniProtKB/TrEMBL
-
G5E879
- Related
- ENSMUSP00000032269.7, ENSMUST00000032269.12
- Conserved Domains (1) summary
-
- TIGR00607
Location:39 → 200
- rad52; recombination protein rad52
RNA
-
NR_149727.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (5) lacks an alternate internal exon, compared to variant 1.This variant is represented as non-coding because the use of the 5'-most expected translational start codon renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AC117667
- Related
-
ENSMUST00000161045.8
-
NR_176974.1 RNA Sequence
Status: VALIDATED
- Source sequence(s)
-
AC117667
-
NR_176975.1 RNA Sequence
Status: VALIDATED
- Source sequence(s)
-
AC117667
-
NR_176977.1 RNA Sequence
Status: VALIDATED
- Source sequence(s)
-
AC117667
-
NR_176978.1 RNA Sequence
Status: VALIDATED
- Source sequence(s)
-
AC117667
-
NR_176979.1 RNA Sequence
Status: VALIDATED
- Source sequence(s)
-
AC117667
-
NR_176980.1 RNA Sequence
Status: VALIDATED
- Source sequence(s)
-
AC117667
The following Reference Sequences have been suppressed. Explain
These RefSeqs were suppressed for the
cited reason(s). Suppressed RefSeqs do not appear in BLAST databases, related
sequence links, or BLAST links (BLink), but may still be retrieved by clicking on
their accession.version below.
-
NM_001166383.1: Suppressed sequence
- Description
- NM_001166383.1: This RefSeq was removed because currently there is insufficient support for the 3'' end of the transcript and the C-terminus of the protein.
-
NR_176976.1: Suppressed sequence
- Description
- NR_176976.1: This RefSeq was removed because of redundancy with NR_176975.1.