Canonical Allele Identifier: CA2259200736
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665799C= , CM000679.2:g.39665799C= GRCh38
NC_000017.10:g.37822052C= , CM000679.1:g.37822052C= GRCh37
NC_000017.9:g.35075578C= NCBI36
NG_008892.1:g.5454C= , LRG_210:g.5454C=
NG_042278.1:g.2819C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.194C= MANE Select ENSP00000312624.2:p.Pro65=
ENST00000309889.2:c.194C= ENSP00000312624.2:p.Pro65=
ENST00000578283.1:c.174+20C= ENSP00000462787.1:n.174+20C=
NM_003673.3:c.194C= , LRG_210t1:c.194C= NP_003664.1:p.Pro65=
NM_003673.4:c.194C= MANE Select NP_003664.1:p.Pro65=