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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_001740.5 → NP_001731.2 calretinin isoform 1
See identical proteins and their annotated locations for NP_001731.2
Status: REVIEWED
- Description
- Transcript Variant: This variant (1) encodes the longer isoform (isoform 1), which has also been designated as the full-length isoform.
- Source sequence(s)
-
AK222495
- Consensus CDS
-
CCDS10899.1
- UniProtKB/Swiss-Prot
- A8K4Y1, P22676, Q53HD2, Q96BK4
- UniProtKB/TrEMBL
- A0A140VK08, H3BN14
- Related
- ENSP00000307508.4, ENST00000302628.9
- Conserved Domains (2) summary
-
- cd00051
Location:111 → 180
- EFh; EF-hand, calcium binding motif; A diverse superfamily of calcium sensors and calcium signal modulators; most examples in this alignment model have 2 active canonical EF hands. Ca2+ binding induces a conformational change in the EF-hand motif, leading to ...
- pfam13499
Location:113 → 180
- EF-hand_7; EF-hand domain pair
-
NM_007088.4 → NP_009019.1 calretinin isoform 22k
See identical proteins and their annotated locations for NP_009019.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (CALB2c) lacks an alternate segment in the 3' coding region, which results in a frameshift and an early stop codon, compared to variant 1. The resulting protein (isoform 22k) has a shorter and distinct C-terminus, compared to isoform 1. There are no publicly available transcripts supporting this variant; it is represented based on data in PMID:7607211.
- Source sequence(s)
-
AK222495
- UniProtKB/TrEMBL
-
A6NER6
- Related
- ENSP00000340294.5, ENST00000349553.9
- Conserved Domains (2) summary
-
- cd00051
Location:111 → 179
- EFh; EF-hand, calcium binding motif; A diverse superfamily of calcium sensors and calcium signal modulators; most examples in this alignment model have 2 active canonical EF hands. Ca2+ binding induces a conformational change in the EF-hand motif, leading to ...
- pfam13499
Location:113 → 176
- EF-hand_7; EF-hand domain pair
RNA
-
NR_027910.3 RNA Sequence
Status: REVIEWED
- Description
- Transcript Variant: This variant (CALB2b) lacks an alternate internal exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD). This variant was described by Schwaller et al (PMID: 7607211), and proposed to encode a 20kDa isoform, but this protein has not been shown to be expressed in vivo.
- Source sequence(s)
-
AK222495
The following sections contain reference sequences that belong to a
specific genome build. Explain
This section includes genomic Reference
Sequences (RefSeqs) from all assemblies on which this gene is annotated, such as
RefSeqs for chromosomes and scaffolds (contigs) from both reference and alternate
assemblies. Model RNAs and proteins are also reported here.
Reference GRCh38.p14 Primary Assembly
Genomic
-
NC_000016.10 Reference GRCh38.p14 Primary Assembly
- Range
-
71358723..71390433
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Reference GRCh38.p14 PATCHES
Genomic
-
NW_013171813.1 Reference GRCh38.p14 PATCHES
- Range
-
226200..257930
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060940.1 Alternate T2T-CHM13v2.0
- Range
-
77174637..77207658
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
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_007087.2: Suppressed sequence
- Description
- NM_007087.2: This RefSeq was permanently suppressed because it is a nonsense-mediated mRNA decay (NMD) candidate.