Canonical Allele Identifier: CA3025119022

Gene: CDH3

Genomic Alleles

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

Transcript Alleles

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