Canonical Allele Identifier: CA1668695988

Gene: VTA1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.142206005A>C , CM000668.2:g.142206005A>C	GRCh38
NC_000006.11:g.142527142A>C , CM000668.1:g.142527142A>C	GRCh37
NC_000006.10:g.142568835A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367630.9:c.778+1940A>C MANE Select	ENSP00000356602.3:n.778+1940A>C
ENST00000367621.1:c.604+1940A>C	ENSP00000356593.1:n.604+1940A>C
ENST00000367630.8:c.778+1940A>C	ENSP00000356602.3:n.778+1940A>C
ENST00000452973.6:c.523+7390A>C	ENSP00000395767.2:n.523+7390A>C
ENST00000620996.4:c.697+7390A>C	ENSP00000481525.1:n.697+7390A>C
NM_001286371.1:c.697+7390A>C	NP_001273300.1:n.697+7390A>C
NM_001286372.1:c.523+7390A>C	NP_001273301.1:n.523+7390A>C
NM_016485.4:c.778+1940A>C	NP_057569.2:n.778+1940A>C
NM_016485.5:c.778+1940A>C MANE Select	NP_057569.2:n.778+1940A>C
NM_001286371.2:c.697+7390A>C	NP_001273300.1:n.697+7390A>C
NM_001286372.2:c.523+7390A>C	NP_001273301.1:n.523+7390A>C