Canonical Allele Identifier: CA2259200835

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665949A= , CM000679.2:g.39665949A=	GRCh38
NC_000017.10:g.37822202A= , CM000679.1:g.37822202A=	GRCh37
NC_000017.9:g.35075728A=	NCBI36
NG_008892.1:g.5604A= , LRG_210:g.5604A=
NG_042278.1:g.2969A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.344A= MANE Select	ENSP00000312624.2:p.Glu115=
ENST00000309889.2:c.344A=	ENSP00000312624.2:p.Glu115=
ENST00000578283.1:c.272A=	ENSP00000462787.1:p.Glu91=
NM_003673.3:c.344A= , LRG_210t1:c.344A=	NP_003664.1:p.Glu115=
NM_003673.4:c.344A= MANE Select	NP_003664.1:p.Glu115=