Canonical Allele Identifier: CA399302916
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665424G>C , CM000679.2:g.39665424G>C GRCh38
NC_000017.10:g.37821677G>C , CM000679.1:g.37821677G>C GRCh37
NC_000017.9:g.35075203G>C NCBI36
NG_008892.1:g.5079G>C , LRG_210:g.5079G>C
NG_042278.1:g.2444G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.65G>C MANE Select ENSP00000312624.2:p.Trp22Ser
ENST00000309889.2:c.65G>C ENSP00000312624.2:p.Trp22Ser
ENST00000578283.1:c.65G>C ENSP00000462787.1:p.Trp22Ser
NM_003673.3:c.65G>C , LRG_210t1:c.65G>C NP_003664.1:p.Trp22Ser
NM_003673.4:c.65G>C MANE Select NP_003664.1:p.Trp22Ser