Canonical Allele Identifier: CA10606859
Gene: TCAP HGNC NCBI

Linked Data

ClinVar Variation Id: 290645
dbSNP Id: rs141019458

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665425G>A , CM000679.2:g.39665425G>A GRCh38
NC_000017.10:g.37821678G>A , CM000679.1:g.37821678G>A GRCh37
NC_000017.9:g.35075204G>A NCBI36
NG_008892.1:g.5080G>A , LRG_210:g.5080G>A
NG_042278.1:g.2445G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000309889.3:c.66G>A MANE Select ENSP00000312624.2:p.Trp22Ter
ENST00000309889.2:c.66G>A ENSP00000312624.2:p.Trp22Ter
ENST00000578283.1:c.66G>A ENSP00000462787.1:p.Trp22Ter
NM_003673.3:c.66G>A , LRG_210t1:c.66G>A NP_003664.1:p.Trp22Ter
NM_003673.4:c.66G>A MANE Select NP_003664.1:p.Trp22Ter