Canonical Allele Identifier: CA8129200

Gene: CDH3

Linked Data

• ClinVar Variation Id: 1368625
• ClinVar RCV Id: RCV001867589
• dbSNP Id: rs121434543
• ExAC: 16:68714968 A / G
• gnomAD v2: 16-68714968-A-G
• gnomAD v3: 16-68681065-A-G
• gnomAD v4: 16-68681065-A-G
• MyVariant Identifiers: chr16:g.68714968A>G (hg19) ; chr16:g.68681065A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68681065A>G , CM000678.2:g.68681065A>G	GRCh38
NC_000016.9:g.68714968A>G , CM000678.1:g.68714968A>G	GRCh37
NC_000016.8:g.67272469A>G	NCBI36
NG_009096.1:g.41818A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264012.9:c.965A>G MANE Select	ENSP00000264012.4:p.Asn322Ser
ENST00000264012.8:c.965A>G	ENSP00000264012.4:p.Asn322Ser
ENST00000429102.6:c.965A>G	ENSP00000398485.2:p.Asn322Ser
ENST00000542274.5:c.*703A>G	ENSP00000464021.1:n.*703A>G
ENST00000569036.2:c.441A>G
NM_001793.4:c.965A>G	NP_001784.2:p.Asn322Ser
XM_011522800.1:c.965A>G	XP_011521102.1:p.Asn322Ser
NM_001317195.1:c.965A>G	NP_001304124.1:p.Asn322Ser
NM_001317196.1:c.800A>G	NP_001304125.1:p.Asn267Ser
NM_001793.5:c.965A>G	NP_001784.2:p.Asn322Ser
XM_011522800.3:c.965A>G	XP_011521102.1:p.Asn322Ser
NM_001793.6:c.965A>G MANE Select	NP_001784.2:p.Asn322Ser
NM_001317195.2:c.965A>G	NP_001304124.1:p.Asn322Ser
NM_001317196.2:c.800A>G	NP_001304125.1:p.Asn267Ser
NM_001317195.3:c.965A>G	NP_001304124.1:p.Asn322Ser