Canonical Allele Identifier: CA2259200509

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665394A= , CM000679.2:g.39665394A=	GRCh38
NC_000017.10:g.37821647A= , CM000679.1:g.37821647A=	GRCh37
NC_000017.9:g.35075173A=	NCBI36
NG_008892.1:g.5049A= , LRG_210:g.5049A=
NG_042278.1:g.2414A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.35A= MANE Select	ENSP00000312624.2:p.Glu12=
ENST00000309889.2:c.35A=	ENSP00000312624.2:p.Glu12=
ENST00000578283.1:c.35A=	ENSP00000462787.1:p.Glu12=
NM_003673.3:c.35A= , LRG_210t1:c.35A=	NP_003664.1:p.Glu12=
NM_003673.4:c.35A= MANE Select	NP_003664.1:p.Glu12=