Canonical Allele Identifier: CA2259200656

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665520A= , CM000679.2:g.39665520A=	GRCh38
NC_000017.10:g.37821773A= , CM000679.1:g.37821773A=	GRCh37
NC_000017.9:g.35075299A=	NCBI36
NG_008892.1:g.5175A= , LRG_210:g.5175A=
NG_042278.1:g.2540A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.110+51A= MANE Select	ENSP00000312624.2:n.110+51A=
ENST00000309889.2:c.110+51A=	ENSP00000312624.2:n.110+51A=
ENST00000578283.1:c.110+51A=	ENSP00000462787.1:n.110+51A=
NM_003673.3:c.110+51A= , LRG_210t1:c.110+51A=	NP_003664.1:n.110+51A=
NM_003673.4:c.110+51A= MANE Select	NP_003664.1:n.110+51A=