Canonical Allele Identifier: CA2259200858

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665999G= , CM000679.2:g.39665999G=	GRCh38
NC_000017.10:g.37822252G= , CM000679.1:g.37822252G=	GRCh37
NC_000017.9:g.35075778G=	NCBI36
NG_008892.1:g.5654G= , LRG_210:g.5654G=
NG_042278.1:g.3019G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.394G= MANE Select	ENSP00000312624.2:p.Glu132=
ENST00000309889.2:c.394G=	ENSP00000312624.2:p.Glu132=
ENST00000578283.1:c.322G=	ENSP00000462787.1:p.Glu108=
NM_003673.3:c.394G= , LRG_210t1:c.394G=	NP_003664.1:p.Glu132=
NM_003673.4:c.394G= MANE Select	NP_003664.1:p.Glu132=