Canonical Allele Identifier: CA2695223569
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829669del , CM000678.2:g.68829669del GRCh38
NC_000016.9:g.68863572del , CM000678.1:g.68863572del GRCh37
NC_000016.8:g.67421073del NCBI36
NG_008021.1:g.97378del , LRG_301:g.97378del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2311del MANE Select ENSP00000261769.4:p.Gln771SerfsTer12
ENST00000261769.9:c.2311del ENSP00000261769.4:p.Gln771SerfsTer12
ENST00000422392.6:c.2128del ENSP00000414946.2:p.Gln710SerfsTer12
ENST00000562118.1:n.529del
ENST00000562836.5:n.2382del
ENST00000566510.5:c.*977del ENSP00000458139.1:n.*977del
ENST00000566612.5:c.*551del ENSP00000454782.1:n.*551del
ENST00000611625.4:c.2374del ENSP00000481063.1:p.Gln792SerfsTer12
ENST00000612417.4:c.1853+3115del ENSP00000478360.1:n.1853+3115del
ENST00000621016.4:c.1866-4534del ENSP00000480664.1:n.1866-4534del
NM_004360.3:c.2311del , LRG_301t1:c.2311del NP_004351.1:p.Gln771SerfsTer12
XM_011523488.1:c.1576del XP_011521790.1:p.Gln526SerfsTer12
XM_011523489.1:c.1576del XP_011521791.1:p.Gln526SerfsTer12
NM_001317184.1:c.2128del NP_001304113.1:p.Gln710SerfsTer12
NM_001317185.1:c.763del NP_001304114.1:p.Gln255SerfsTer12
NM_001317186.1:c.346del NP_001304115.1:p.Gln116SerfsTer12
NM_004360.4:c.2311del NP_004351.1:p.Gln771SerfsTer12
NM_004360.5:c.2311del MANE Select NP_004351.1:p.Gln771SerfsTer12
NM_001317184.2:c.2128del NP_001304113.1:p.Gln710SerfsTer12
NM_001317185.2:c.763del NP_001304114.1:p.Gln255SerfsTer12
NM_001317186.2:c.346del NP_001304115.1:p.Gln116SerfsTer12