Canonical Allele Identifier: CA2259200697
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665781T= , CM000679.2:g.39665781T= GRCh38
NC_000017.10:g.37822034T= , CM000679.1:g.37822034T= GRCh37
NC_000017.9:g.35075560T= NCBI36
NG_008892.1:g.5436T= , LRG_210:g.5436T=
NG_042278.1:g.2801T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.176T= MANE Select ENSP00000312624.2:p.Val59=
ENST00000309889.2:c.176T= ENSP00000312624.2:p.Val59=
ENST00000578283.1:c.174+2T= ENSP00000462787.1:n.174+2T=
NM_003673.3:c.176T= , LRG_210t1:c.176T= NP_003664.1:p.Val59=
NM_003673.4:c.176T= MANE Select NP_003664.1:p.Val59=