Canonical Allele Identifier: CA2259200831

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665942C= , CM000679.2:g.39665942C=	GRCh38
NC_000017.10:g.37822195C= , CM000679.1:g.37822195C=	GRCh37
NC_000017.9:g.35075721C=	NCBI36
NG_008892.1:g.5597C= , LRG_210:g.5597C=
NG_042278.1:g.2962C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.337C= MANE Select	ENSP00000312624.2:p.Leu113=
ENST00000309889.2:c.337C=	ENSP00000312624.2:p.Leu113=
ENST00000578283.1:c.265C=	ENSP00000462787.1:p.Leu89=
NM_003673.3:c.337C= , LRG_210t1:c.337C=	NP_003664.1:p.Leu113=
NM_003673.4:c.337C= MANE Select	NP_003664.1:p.Leu113=