Canonical Allele Identifier: CA2229884338

Gene: CDH3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68680973C= , CM000678.2:g.68680973C=	GRCh38
NC_000016.9:g.68714876C= , CM000678.1:g.68714876C=	GRCh37
NC_000016.8:g.67272377C=	NCBI36
NG_009096.1:g.41726C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264012.9:c.873C= MANE Select	ENSP00000264012.4:p.Val291=
ENST00000264012.8:c.873C=	ENSP00000264012.4:p.Val291=
ENST00000429102.6:c.873C=	ENSP00000398485.2:p.Val291=
ENST00000542274.5:c.*611C=	ENSP00000464021.1:n.*611C=
ENST00000569036.2:c.349C=
NM_001793.4:c.873C=	NP_001784.2:p.Val291=
XM_011522800.1:c.873C=	XP_011521102.1:p.Val291=
NM_001317195.1:c.873C=	NP_001304124.1:p.Val291=
NM_001317196.1:c.708C=	NP_001304125.1:p.Val236=
NM_001793.5:c.873C=	NP_001784.2:p.Val291=
XM_011522800.3:c.873C=	XP_011521102.1:p.Val291=
NM_001793.6:c.873C= MANE Select	NP_001784.2:p.Val291=
NM_001317195.2:c.873C=	NP_001304124.1:p.Val291=
NM_001317196.2:c.708C=	NP_001304125.1:p.Val236=
NM_001317195.3:c.873C=	NP_001304124.1:p.Val291=