Canonical Allele Identifier: CA396455060

Gene: CDH3

Linked Data

• ClinVar Variation Id: 3141266
• ClinVar RCV Id: RCV004428122
• gnomAD v4: 16-68645383-G-C
• MyVariant Identifiers: chr16:g.68679286G>C (hg19) ; chr16:g.68645383G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68645383G>C , CM000678.2:g.68645383G>C	GRCh38
NC_000016.9:g.68679286G>C , CM000678.1:g.68679286G>C	GRCh37
NC_000016.8:g.67236787G>C	NCBI36
NG_009096.1:g.6136G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264012.9:c.4G>C MANE Select	ENSP00000264012.4:p.Gly2Arg
ENST00000264012.8:c.4G>C	ENSP00000264012.4:p.Gly2Arg
ENST00000429102.6:c.4G>C	ENSP00000398485.2:p.Gly2Arg
ENST00000542274.5:c.4G>C	ENSP00000464021.1:p.Gly2Arg
NM_001793.4:c.4G>C	NP_001784.2:p.Gly2Arg
XM_011522800.1:c.4G>C	XP_011521102.1:p.Gly2Arg
NM_001317195.1:c.4G>C	NP_001304124.1:p.Gly2Arg
NM_001317196.1:c.-47G>C	NP_001304125.1:n.-47G>C
NM_001793.5:c.4G>C	NP_001784.2:p.Gly2Arg
XM_011522800.3:c.4G>C	XP_011521102.1:p.Gly2Arg
NM_001793.6:c.4G>C MANE Select	NP_001784.2:p.Gly2Arg
NM_001317195.2:c.4G>C	NP_001304124.1:p.Gly2Arg
NM_001317196.2:c.-47G>C	NP_001304125.1:n.-47G>C
NM_001317195.3:c.4G>C	NP_001304124.1:p.Gly2Arg