Canonical Allele Identifier: CA283273984

Gene: CDH3

Linked Data

• ClinVar Variation Id: 1947510
• ClinVar RCV Id: RCV002685513
• dbSNP Id: rs369749641
• gnomAD v2: 16-68714876-C-G
• gnomAD v3: 16-68680973-C-G
• gnomAD v4: 16-68680973-C-G
• MyVariant Identifiers: chr16:g.68714876C>G (hg19) ; chr16:g.68680973C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68680973C>G , CM000678.2:g.68680973C>G	GRCh38
NC_000016.9:g.68714876C>G , CM000678.1:g.68714876C>G	GRCh37
NC_000016.8:g.67272377C>G	NCBI36
NG_009096.1:g.41726C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264012.9:c.873C>G MANE Select	ENSP00000264012.4:p.Val291=
ENST00000264012.8:c.873C>G	ENSP00000264012.4:p.Val291=
ENST00000429102.6:c.873C>G	ENSP00000398485.2:p.Val291=
ENST00000542274.5:c.*611C>G	ENSP00000464021.1:n.*611C>G
ENST00000569036.2:c.349C>G
NM_001793.4:c.873C>G	NP_001784.2:p.Val291=
XM_011522800.1:c.873C>G	XP_011521102.1:p.Val291=
NM_001317195.1:c.873C>G	NP_001304124.1:p.Val291=
NM_001317196.1:c.708C>G	NP_001304125.1:p.Val236=
NM_001793.5:c.873C>G	NP_001784.2:p.Val291=
XM_011522800.3:c.873C>G	XP_011521102.1:p.Val291=
NM_001793.6:c.873C>G MANE Select	NP_001784.2:p.Val291=
NM_001317195.2:c.873C>G	NP_001304124.1:p.Val291=
NM_001317196.2:c.708C>G	NP_001304125.1:p.Val236=
NM_001317195.3:c.873C>G	NP_001304124.1:p.Val291=