Canonical Allele Identifier: CA2259200889

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39666057C= , CM000679.2:g.39666057C=	GRCh38
NC_000017.10:g.37822310C= , CM000679.1:g.37822310C=	GRCh37
NC_000017.9:g.35075836C=	NCBI36
NG_008892.1:g.5712C= , LRG_210:g.5712C=
NG_042278.1:g.3077C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.452C= MANE Select	ENSP00000312624.2:p.Ala151=
ENST00000309889.2:c.452C=	ENSP00000312624.2:p.Ala151=
ENST00000578283.1:c.380C=	ENSP00000462787.1:p.Ala127=
NM_003673.3:c.452C= , LRG_210t1:c.452C=	NP_003664.1:p.Ala151=
NM_003673.4:c.452C= MANE Select	NP_003664.1:p.Ala151=