Canonical Allele Identifier: CA396451519

Gene: CDH3

Linked Data

• gnomAD v4: 16-68680972-T-C
• MyVariant Identifiers: chr16:g.68714875T>C (hg19) ; chr16:g.68680972T>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264012.9:c.872T>C MANE Select	ENSP00000264012.4:p.Val291Ala
ENST00000264012.8:c.872T>C	ENSP00000264012.4:p.Val291Ala
ENST00000429102.6:c.872T>C	ENSP00000398485.2:p.Val291Ala
ENST00000542274.5:c.*610T>C	ENSP00000464021.1:n.*610T>C
ENST00000569036.2:c.348T>C
NM_001793.4:c.872T>C	NP_001784.2:p.Val291Ala
XM_011522800.1:c.872T>C	XP_011521102.1:p.Val291Ala
NM_001317195.1:c.872T>C	NP_001304124.1:p.Val291Ala
NM_001317196.1:c.707T>C	NP_001304125.1:p.Val236Ala
NM_001793.5:c.872T>C	NP_001784.2:p.Val291Ala
XM_011522800.3:c.872T>C	XP_011521102.1:p.Val291Ala
NM_001793.6:c.872T>C MANE Select	NP_001784.2:p.Val291Ala
NM_001317195.2:c.872T>C	NP_001304124.1:p.Val291Ala
NM_001317196.2:c.707T>C	NP_001304125.1:p.Val236Ala
NM_001317195.3:c.872T>C	NP_001304124.1:p.Val291Ala