Description

ventral anterior homeobox 1 [Source:HGNC Symbol;Acc:HGNC:12660]

INSDC coordinates

chromosome:GRCh38:CM000672.2:117128521:117138301:1

Transcripts

This gene has 2 transcripts (splice variants) Show transcript tableHide transcript table

NameTranscript IDbpProteinBiotypeCCDSUniProtRefSeqFlags
VAX1-002ENST000002779054494186 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS7597Q5SQQ9 NM_199131
NP_954582
TSL:1

TSL1: All splice junctions of the transcript are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).
VAX1-001ENST000003692061723334 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS44483Q5SQQ9 NM_001112704
NP_001106175
TSL:5

TSL5: No single transcript (mRNA or EST) supports this transcript model's structure.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS PIAPPRIS principal isoform
Glossary entry for APPRIS
APPRIS website

Gene-based displays