Canonical Allele Identifier: CA8532886
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs781560443

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665869A>T , CM000679.2:g.39665869A>T GRCh38
NC_000017.10:g.37822122A>T , CM000679.1:g.37822122A>T GRCh37
NC_000017.9:g.35075648A>T NCBI36
NG_008892.1:g.5524A>T , LRG_210:g.5524A>T
NG_042278.1:g.2889A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000309889.3:c.264A>T MANE Select ENSP00000312624.2:p.Val88=
ENST00000309889.2:c.264A>T ENSP00000312624.2:p.Val88=
ENST00000578283.1:c.192A>T ENSP00000462787.1:p.Val64=
NM_003673.3:c.264A>T , LRG_210t1:c.264A>T NP_003664.1:p.Val88=
NM_003673.4:c.264A>T MANE Select NP_003664.1:p.Val88=