Human (GRCh38.p14)
Description

V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]

Gene Synonyms

UNQ3033

Location

Chromosome 19: 54,040,825-54,063,953 reverse strand.

GRCh38:CM000681.2

View alleles of this gene on alternative sequences

About this gene

This gene has 7 transcripts (splice variants), 1 gene allele, 209 orthologues and 25 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000338372.7VSTM1-201967236aaENSP00000343366.2
 
Protein coding
CCDS12872Q6UX27-1 NM_198481.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P2TSL:1
ENST00000376626.5VSTM1-203922205aaENSP00000365813.1
 
Protein coding
CCDS74442Q6UX27-2 -GENCODE basicAPPRIS ALT2TSL:1
ENST00000645936.1VSTM1-207854229aaENSP00000495014.1
 
Protein coding
A0A2R8Y636 -CDS 3' incomplete
ENST00000366170.6VSTM1-202654116aaENSP00000444153.2
 
Protein coding
CCDS74441D2DJS5 -GENCODE basicTSL:1
ENST00000425006.3VSTM1-205608143aaENSP00000413006.2
 
Protein coding
G8JLN4 -GENCODE basicAPPRIS ALT2TSL:5
ENST00000419106.5VSTM1-204517126aaENSP00000409412.1
 
Protein coding
H7C340 -TSL:2CDS 5' incomplete
ENST00000447872.5VSTM1-2061041174aaENSP00000401926.1
 
Nonsense mediated decay
Q6UX27-3 -TSL:1