Canonical Allele Identifier: CA8129251

Gene: CDH3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68682391G>A , CM000678.2:g.68682391G>A	GRCh38
NC_000016.9:g.68716294G>A , CM000678.1:g.68716294G>A	GRCh37
NC_000016.8:g.67273795G>A	NCBI36
NG_009096.1:g.43144G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001793.6:c.1086G>A MANE Select	NP_001784.2:p.Trp362Ter
ENST00000264012.9:c.1086G>A MANE Select	ENSP00000264012.4:p.Trp362Ter
NM_001317195.1:c.1086G>A	NP_001304124.1:p.Trp362Ter
NM_001317195.2:c.1086G>A	NP_001304124.1:p.Trp362Ter
NM_001317195.3:c.1086G>A	NP_001304124.1:p.Trp362Ter
NM_001317196.1:c.921G>A	NP_001304125.1:p.Trp307Ter
NM_001317196.2:c.921G>A	NP_001304125.1:p.Trp307Ter
NM_001793.4:c.1086G>A	NP_001784.2:p.Trp362Ter
NM_001793.5:c.1086G>A	NP_001784.2:p.Trp362Ter
ENST00000264012.8:c.1086G>A	ENSP00000264012.4:p.Trp362Ter
ENST00000429102.6:c.1086G>A	ENSP00000398485.2:p.Trp362Ter
ENST00000542274.5:c.*824G>A	ENSP00000464021.1:n.*824G>A
ENST00000569036.2:c.562G>A
XM_011522800.1:c.1086G>A	XP_011521102.1:p.Trp362Ter
XM_011522800.3:c.1086G>A	XP_011521102.1:p.Trp362Ter