Canonical Allele Identifier: CA8129045

Gene: CDH3

Linked Data

• ClinVar Variation Id: 1402815
• ClinVar RCV Id: RCV001908732 ; RCV002507002
• dbSNP Id: rs773525226
• ExAC: 16:68712488 G / A
• gnomAD v2: 16-68712488-G-A
• gnomAD v3: 16-68678585-G-A
• gnomAD v4: 16-68678585-G-A
• MyVariant Identifiers: chr16:g.68712488G>A (hg19) ; chr16:g.68678585G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68678585G>A , CM000678.2:g.68678585G>A	GRCh38
NC_000016.9:g.68712488G>A , CM000678.1:g.68712488G>A	GRCh37
NC_000016.8:g.67269989G>A	NCBI36
NG_009096.1:g.39338G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264012.9:c.475G>A MANE Select	ENSP00000264012.4:p.Ala159Thr
ENST00000264012.8:c.475G>A	ENSP00000264012.4:p.Ala159Thr
ENST00000429102.6:c.475G>A	ENSP00000398485.2:p.Ala159Thr
ENST00000542274.5:c.*213G>A	ENSP00000464021.1:n.*213G>A
ENST00000566808.2:c.343G>A
ENST00000569036.2:c.96G>A
NM_001793.4:c.475G>A	NP_001784.2:p.Ala159Thr
XM_011522800.1:c.475G>A	XP_011521102.1:p.Ala159Thr
NM_001317195.1:c.475G>A	NP_001304124.1:p.Ala159Thr
NM_001317196.1:c.310G>A	NP_001304125.1:p.Ala104Thr
NM_001793.5:c.475G>A	NP_001784.2:p.Ala159Thr
XM_011522800.3:c.475G>A	XP_011521102.1:p.Ala159Thr
NM_001793.6:c.475G>A MANE Select	NP_001784.2:p.Ala159Thr
NM_001317195.2:c.475G>A	NP_001304124.1:p.Ala159Thr
NM_001317196.2:c.310G>A	NP_001304125.1:p.Ala104Thr
NM_001317195.3:c.475G>A	NP_001304124.1:p.Ala159Thr