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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_001320037.2 → NP_001306966.1 uncharacterized protein LOC730098
Status: VALIDATED
- Description
- Transcript Variant: This variant (1) represents the shorter transcript. Both variants 1 and 2 encode the same protein.
- Source sequence(s)
-
AK296005, AL162231, HY158194
- Consensus CDS
-
CCDS83357.1
- UniProtKB/TrEMBL
- D3DRN1, G3V523
- Related
- ENSP00000452132.1, ENST00000544078.2
-
NM_001320038.2 → NP_001306967.1 uncharacterized protein LOC730098
Status: VALIDATED
- Description
- Transcript Variant: This variant (2) retains an intron in the 5' UTR compared to variant 1. Both variants 1 and 2 encode the same protein.
- Source sequence(s)
-
AK296005, AL162231, BC066358
- Consensus CDS
-
CCDS83357.1
- UniProtKB/TrEMBL
- D3DRN1, G3V523
- Related
- ENSP00000457701.1, ENST00000421828.7
RNA
-
NR_135148.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (3) retains an intron compared to variant 1. This variant is represented as non-coding because the predicted protein does not meet RefSeq quality criteria.
- Source sequence(s)
-
AK296005, AL162231, BM695963, DB061900, HY030992
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_000009.12 Reference GRCh38.p14 Primary Assembly
- Range
-
34664163..34666045 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060933.1 Alternate T2T-CHM13v2.0
- Range
-
34682692..34684574 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)