Canonical Allele Identifier: CA396451517

Gene: CDH3

Linked Data

• MyVariant Identifiers: chr16:g.68714875T>A (hg19) ; chr16:g.68680972T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68680972T>A , CM000678.2:g.68680972T>A	GRCh38
NC_000016.9:g.68714875T>A , CM000678.1:g.68714875T>A	GRCh37
NC_000016.8:g.67272376T>A	NCBI36
NG_009096.1:g.41725T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264012.9:c.872T>A MANE Select	ENSP00000264012.4:p.Val291Asp
ENST00000264012.8:c.872T>A	ENSP00000264012.4:p.Val291Asp
ENST00000429102.6:c.872T>A	ENSP00000398485.2:p.Val291Asp
ENST00000542274.5:c.*610T>A	ENSP00000464021.1:n.*610T>A
ENST00000569036.2:c.348T>A
NM_001793.4:c.872T>A	NP_001784.2:p.Val291Asp
XM_011522800.1:c.872T>A	XP_011521102.1:p.Val291Asp
NM_001317195.1:c.872T>A	NP_001304124.1:p.Val291Asp
NM_001317196.1:c.707T>A	NP_001304125.1:p.Val236Asp
NM_001793.5:c.872T>A	NP_001784.2:p.Val291Asp
XM_011522800.3:c.872T>A	XP_011521102.1:p.Val291Asp
NM_001793.6:c.872T>A MANE Select	NP_001784.2:p.Val291Asp
NM_001317195.2:c.872T>A	NP_001304124.1:p.Val291Asp
NM_001317196.2:c.707T>A	NP_001304125.1:p.Val236Asp
NM_001317195.3:c.872T>A	NP_001304124.1:p.Val291Asp