Canonical Allele Identifier: CA2259200853

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665991A= , CM000679.2:g.39665991A=	GRCh38
NC_000017.10:g.37822244A= , CM000679.1:g.37822244A=	GRCh37
NC_000017.9:g.35075770A=	NCBI36
NG_008892.1:g.5646A= , LRG_210:g.5646A=
NG_042278.1:g.3011A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.386A= MANE Select	ENSP00000312624.2:p.Asp129=
ENST00000309889.2:c.386A=	ENSP00000312624.2:p.Asp129=
ENST00000578283.1:c.314A=	ENSP00000462787.1:p.Asp105=
NM_003673.3:c.386A= , LRG_210t1:c.386A=	NP_003664.1:p.Asp129=
NM_003673.4:c.386A= MANE Select	NP_003664.1:p.Asp129=