Canonical Allele Identifier: CA2259200839

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665959G= , CM000679.2:g.39665959G=	GRCh38
NC_000017.10:g.37822212G= , CM000679.1:g.37822212G=	GRCh37
NC_000017.9:g.35075738G=	NCBI36
NG_008892.1:g.5614G= , LRG_210:g.5614G=
NG_042278.1:g.2979G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.354G= MANE Select	ENSP00000312624.2:p.Ala118=
ENST00000309889.2:c.354G=	ENSP00000312624.2:p.Ala118=
ENST00000578283.1:c.282G=	ENSP00000462787.1:p.Ala94=
NM_003673.3:c.354G= , LRG_210t1:c.354G=	NP_003664.1:p.Ala118=
NM_003673.4:c.354G= MANE Select	NP_003664.1:p.Ala118=