Canonical Allele Identifier: CA2259200766

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665817T= , CM000679.2:g.39665817T=	GRCh38
NC_000017.10:g.37822070T= , CM000679.1:g.37822070T=	GRCh37
NC_000017.9:g.35075596T=	NCBI36
NG_008892.1:g.5472T= , LRG_210:g.5472T=
NG_042278.1:g.2837T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.212T= MANE Select	ENSP00000312624.2:p.Met71=
ENST00000309889.2:c.212T=	ENSP00000312624.2:p.Met71=
ENST00000578283.1:c.175-35T=	ENSP00000462787.1:n.175-35T=
NM_003673.3:c.212T= , LRG_210t1:c.212T=	NP_003664.1:p.Met71=
NM_003673.4:c.212T= MANE Select	NP_003664.1:p.Met71=