Canonical Allele Identifier: CA2259200700

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665782G= , CM000679.2:g.39665782G=	GRCh38
NC_000017.10:g.37822035G= , CM000679.1:g.37822035G=	GRCh37
NC_000017.9:g.35075561G=	NCBI36
NG_008892.1:g.5437G= , LRG_210:g.5437G=
NG_042278.1:g.2802G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.177G= MANE Select	ENSP00000312624.2:p.Val59=
ENST00000309889.2:c.177G=	ENSP00000312624.2:p.Val59=
ENST00000578283.1:c.174+3G=	ENSP00000462787.1:n.174+3G=
NM_003673.3:c.177G= , LRG_210t1:c.177G=	NP_003664.1:p.Val59=
NM_003673.4:c.177G= MANE Select	NP_003664.1:p.Val59=