Canonical Allele Identifier: CA2259200769

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665823T= , CM000679.2:g.39665823T=	GRCh38
NC_000017.10:g.37822076T= , CM000679.1:g.37822076T=	GRCh37
NC_000017.9:g.35075602T=	NCBI36
NG_008892.1:g.5478T= , LRG_210:g.5478T=
NG_042278.1:g.2843T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.218T= MANE Select	ENSP00000312624.2:p.Ile73=
ENST00000309889.2:c.218T=	ENSP00000312624.2:p.Ile73=
ENST00000578283.1:c.175-29T=	ENSP00000462787.1:n.175-29T=
NM_003673.3:c.218T= , LRG_210t1:c.218T=	NP_003664.1:p.Ile73=
NM_003673.4:c.218T= MANE Select	NP_003664.1:p.Ile73=