Canonical Allele Identifier: CA396455404

Gene: CDH3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68645751G>A , CM000678.2:g.68645751G>A	GRCh38
NC_000016.9:g.68679654G>A , CM000678.1:g.68679654G>A	GRCh37
NC_000016.8:g.67237155G>A	NCBI36
NG_009096.1:g.6504G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001793.6:c.160+1G>A MANE Select	NP_001784.2:n.160+1G>A
ENST00000264012.9:c.160+1G>A MANE Select	ENSP00000264012.4:n.160+1G>A
NM_001317195.1:c.160+1G>A	NP_001304124.1:n.160+1G>A
NM_001317195.2:c.160+1G>A	NP_001304124.1:n.160+1G>A
NM_001317195.3:c.160+1G>A	NP_001304124.1:n.160+1G>A
NM_001317196.1:c.-6+327G>A	NP_001304125.1:n.-6+327G>A
NM_001317196.2:c.-6+327G>A	NP_001304125.1:n.-6+327G>A
NM_001793.4:c.160+1G>A	NP_001784.2:n.160+1G>A
NM_001793.5:c.160+1G>A	NP_001784.2:n.160+1G>A
ENST00000264012.8:c.160+1G>A	ENSP00000264012.4:n.160+1G>A
ENST00000429102.6:c.160+1G>A	ENSP00000398485.2:n.160+1G>A
ENST00000542274.5:c.45+327G>A	ENSP00000464021.1:n.45+327G>A
ENST00000566808.2:c.114+1G>A
XM_011522800.1:c.160+1G>A	XP_011521102.1:n.160+1G>A
XM_011522800.3:c.160+1G>A	XP_011521102.1:n.160+1G>A