Canonical Allele Identifier: CA2259200637

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665496C= , CM000679.2:g.39665496C=	GRCh38
NC_000017.10:g.37821749C= , CM000679.1:g.37821749C=	GRCh37
NC_000017.9:g.35075275C=	NCBI36
NG_008892.1:g.5151C= , LRG_210:g.5151C=
NG_042278.1:g.2516C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.110+27C= MANE Select	ENSP00000312624.2:n.110+27C=
ENST00000309889.2:c.110+27C=	ENSP00000312624.2:n.110+27C=
ENST00000578283.1:c.110+27C=	ENSP00000462787.1:n.110+27C=
NM_003673.3:c.110+27C= , LRG_210t1:c.110+27C=	NP_003664.1:n.110+27C=
NM_003673.4:c.110+27C= MANE Select	NP_003664.1:n.110+27C=