Canonical Allele Identifier: CA396472896

Gene: CDH1

Linked Data

• ClinVar Variation Id: 2897774
• ClinVar RCV Id: RCV003624283
• dbSNP Id: rs1567517888
• MyVariant Identifiers: chr16:g.68867389G>A (hg19) ; chr16:g.68833486G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833486G>A , CM000678.2:g.68833486G>A	GRCh38
NC_000016.9:g.68867389G>A , CM000678.1:g.68867389G>A	GRCh37
NC_000016.8:g.67424890G>A	NCBI36
NG_008021.1:g.101195G>A , LRG_301:g.101195G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2636G>A MANE Select	ENSP00000261769.4:p.Gly879Asp
ENST00000261769.9:c.2636G>A	ENSP00000261769.4:p.Gly879Asp
ENST00000422392.6:c.2453G>A	ENSP00000414946.2:p.Gly818Asp
ENST00000562118.1:n.854G>A
ENST00000562836.5:n.2707G>A
ENST00000566510.5:c.*1302G>A	ENSP00000458139.1:n.*1302G>A
ENST00000566612.5:c.*876G>A	ENSP00000454782.1:n.*876G>A
ENST00000611625.4:c.2699G>A	ENSP00000481063.1:p.Gly900Asp
ENST00000612417.4:c.1854-705G>A	ENSP00000478360.1:n.1854-705G>A
ENST00000621016.4:c.1866-717G>A	ENSP00000480664.1:n.1866-717G>A
NM_004360.3:c.2636G>A , LRG_301t1:c.2636G>A	NP_004351.1:p.Gly879Asp
XM_011523488.1:c.1901G>A	XP_011521790.1:p.Gly634Asp
XM_011523489.1:c.1901G>A	XP_011521791.1:p.Gly634Asp
NM_001317184.1:c.2453G>A	NP_001304113.1:p.Gly818Asp
NM_001317185.1:c.1088G>A	NP_001304114.1:p.Gly363Asp
NM_001317186.1:c.671G>A	NP_001304115.1:p.Gly224Asp
NM_004360.4:c.2636G>A	NP_004351.1:p.Gly879Asp
NM_004360.5:c.2636G>A MANE Select	NP_004351.1:p.Gly879Asp
NM_001317184.2:c.2453G>A	NP_001304113.1:p.Gly818Asp
NM_001317185.2:c.1088G>A	NP_001304114.1:p.Gly363Asp
NM_001317186.2:c.671G>A	NP_001304115.1:p.Gly224Asp