Canonical Allele Identifier: CA3222449942

Gene: CDH3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68699042T= , CM000678.2:g.68699042T=	GRCh38
NC_000016.9:g.68732945T= , CM000678.1:g.68732945T=	GRCh37
NC_000016.8:g.67290446T=	NCBI36
NG_009096.1:g.59795T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001793.6:c.*642T= MANE Select	NP_001784.2:n.*642T=
ENST00000264012.9:c.*642T= MANE Select	ENSP00000264012.4:n.*642T=
NM_001317195.1:c.*875T=	NP_001304124.1:n.*875T=
NM_001317195.2:c.*875T=	NP_001304124.1:n.*875T=
NM_001317196.1:c.*642T=	NP_001304125.1:n.*642T=
NM_001317196.2:c.*642T=	NP_001304125.1:n.*642T=
NM_001793.4:c.*642T=	NP_001784.2:n.*642T=
NM_001793.5:c.*642T=	NP_001784.2:n.*642T=
ENST00000264012.8:c.*642T=	ENSP00000264012.4:n.*642T=
ENST00000569080.1:c.99+3119T=	ENSP00000463415.1:n.99+3119T=
ENST00000569080.2:c.99+3119T=	ENSP00000463415.1:n.99+3119T=
XM_011522800.1:c.2280+3119T=	XP_011521102.1:n.2280+3119T=
XM_011522800.3:c.2280+3119T=	XP_011521102.1:n.2280+3119T=