Canonical Allele Identifier: CA396466138

Gene: CDH1

Linked Data

• ClinVar Variation Id: 1462505
• ClinVar RCV Id: RCV001968511 ; RCV003365606
• dbSNP Id: rs1961155617
• gnomAD v3: 16-68822001-G-A
• gnomAD v4: 16-68822001-G-A
• MyVariant Identifiers: chr16:g.68855904G>A (hg19) ; chr16:g.68822001G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822001G>A , CM000678.2:g.68822001G>A	GRCh38
NC_000016.9:g.68855904G>A , CM000678.1:g.68855904G>A	GRCh37
NC_000016.8:g.67413405G>A	NCBI36
NG_008021.1:g.89710G>A , LRG_301:g.89710G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1712G>A MANE Select	ENSP00000261769.4:p.Gly571Asp
ENST00000261769.9:c.1712G>A	ENSP00000261769.4:p.Gly571Asp
ENST00000422392.6:c.1529G>A	ENSP00000414946.2:p.Gly510Asp
ENST00000562836.5:n.1783G>A
ENST00000566510.5:c.*378G>A	ENSP00000458139.1:n.*378G>A
ENST00000566612.5:c.1566G>A	ENSP00000454782.1:p.Thr522=
ENST00000611625.4:c.1775G>A	ENSP00000481063.1:p.Gly592Asp
ENST00000612417.4:c.1712G>A	ENSP00000478360.1:p.Gly571Asp
ENST00000621016.4:c.1712G>A	ENSP00000480664.1:p.Gly571Asp
NM_004360.3:c.1712G>A , LRG_301t1:c.1712G>A	NP_004351.1:p.Gly571Asp
XM_011523488.1:c.977G>A	XP_011521790.1:p.Gly326Asp
XM_011523489.1:c.977G>A	XP_011521791.1:p.Gly326Asp
NM_001317184.1:c.1529G>A	NP_001304113.1:p.Gly510Asp
NM_001317185.1:c.164G>A	NP_001304114.1:p.Gly55Asp
NM_001317186.1:c.-254G>A	NP_001304115.1:n.-254G>A
NM_004360.4:c.1712G>A	NP_004351.1:p.Gly571Asp
NM_004360.5:c.1712G>A MANE Select	NP_004351.1:p.Gly571Asp
NM_001317184.2:c.1529G>A	NP_001304113.1:p.Gly510Asp
NM_001317185.2:c.164G>A	NP_001304114.1:p.Gly55Asp
NM_001317186.2:c.-254G>A	NP_001304115.1:n.-254G>A