Canonical Allele Identifier: CA8129518

Gene: CDH3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68691880G>A , CM000678.2:g.68691880G>A	GRCh38
NC_000016.9:g.68725783G>A , CM000678.1:g.68725783G>A	GRCh37
NC_000016.8:g.67283284G>A	NCBI36
NG_009096.1:g.52633G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001793.6:c.1956G>A MANE Select	NP_001784.2:p.Lys652=
ENST00000264012.9:c.1956G>A MANE Select	ENSP00000264012.4:p.Lys652=
NM_001317195.1:c.1956G>A	NP_001304124.1:p.Lys652=
NM_001317195.2:c.1956G>A	NP_001304124.1:p.Lys652=
NM_001317195.3:c.1956G>A	NP_001304124.1:p.Lys652=
NM_001317196.1:c.1791G>A	NP_001304125.1:p.Lys597=
NM_001317196.2:c.1791G>A	NP_001304125.1:p.Lys597=
NM_001793.4:c.1956G>A	NP_001784.2:p.Lys652=
NM_001793.5:c.1956G>A	NP_001784.2:p.Lys652=
ENST00000264012.8:c.1956G>A	ENSP00000264012.4:p.Lys652=
ENST00000429102.6:c.1956G>A	ENSP00000398485.2:p.Lys652=
ENST00000542274.5:c.*1694G>A	ENSP00000464021.1:n.*1694G>A
ENST00000567674.1:c.286G>A
ENST00000568292.1:c.35G>A
XM_011522800.1:c.1956G>A	XP_011521102.1:p.Lys652=
XM_011522800.3:c.1956G>A	XP_011521102.1:p.Lys652=