Canonical Allele Identifier: CA8128894

Gene: CDH3

Linked Data

• ClinVar Variation Id: 320222
• ClinVar RCV Id: RCV000401003
• dbSNP Id: rs370893872
• ExAC: 16:68679272 T / C
• gnomAD v2: 16-68679272-T-C
• gnomAD v3: 16-68645369-T-C
• gnomAD v4: 16-68645369-T-C
• MyVariant Identifiers: chr16:g.68679272T>C (hg19) ; chr16:g.68645369T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68645369T>C , CM000678.2:g.68645369T>C	GRCh38
NC_000016.9:g.68679272T>C , CM000678.1:g.68679272T>C	GRCh37
NC_000016.8:g.67236773T>C	NCBI36
NG_009096.1:g.6122T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264012.9:c.-11T>C MANE Select	ENSP00000264012.4:n.-11T>C
ENST00000264012.8:c.-11T>C	ENSP00000264012.4:n.-11T>C
ENST00000429102.6:c.-11T>C	ENSP00000398485.2:n.-11T>C
ENST00000542274.5:c.-11T>C	ENSP00000464021.1:n.-11T>C
NM_001793.4:c.-11T>C	NP_001784.2:n.-11T>C
XM_011522800.1:c.-11T>C	XP_011521102.1:n.-11T>C
NM_001317195.1:c.-11T>C	NP_001304124.1:n.-11T>C
NM_001317196.1:c.-61T>C	NP_001304125.1:n.-61T>C
NM_001793.5:c.-11T>C	NP_001784.2:n.-11T>C
XM_011522800.3:c.-11T>C	XP_011521102.1:n.-11T>C
NM_001793.6:c.-11T>C MANE Select	NP_001784.2:n.-11T>C
NM_001317195.2:c.-11T>C	NP_001304124.1:n.-11T>C
NM_001317196.2:c.-61T>C	NP_001304125.1:n.-61T>C
NM_001317195.3:c.-11T>C	NP_001304124.1:n.-11T>C