Canonical Allele Identifier: CA2807471363
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68823499del , CM000678.2:g.68823499del GRCh38
NC_000016.9:g.68857402del , CM000678.1:g.68857402del GRCh37
NC_000016.8:g.67414903del NCBI36
NG_008021.1:g.91208del , LRG_301:g.91208del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2037del MANE Select ENSP00000261769.4:p.Thr680ProfsTer2
ENST00000261769.9:c.2037del ENSP00000261769.4:p.Thr680ProfsTer2
ENST00000422392.6:c.1854del ENSP00000414946.2:p.Thr619ProfsTer2
ENST00000562118.1:n.255del
ENST00000562836.5:n.2108del
ENST00000566510.5:c.*703del ENSP00000458139.1:n.*703del
ENST00000566612.5:c.*277del ENSP00000454782.1:n.*277del
ENST00000611625.4:c.2100del ENSP00000481063.1:p.Thr701ProfsTer2
ENST00000612417.4:c.1830+1380del ENSP00000478360.1:n.1830+1380del
ENST00000621016.4:c.1865+1345del ENSP00000480664.1:n.1865+1345del
NM_004360.3:c.2037del , LRG_301t1:c.2037del NP_004351.1:p.Thr680ProfsTer2
XM_011523488.1:c.1302del XP_011521790.1:p.Thr435ProfsTer2
XM_011523489.1:c.1302del XP_011521791.1:p.Thr435ProfsTer2
NM_001317184.1:c.1854del NP_001304113.1:p.Thr619ProfsTer2
NM_001317185.1:c.489del NP_001304114.1:p.Thr164ProfsTer2
NM_001317186.1:c.72del NP_001304115.1:p.Thr25ProfsTer2
NM_004360.4:c.2037del NP_004351.1:p.Thr680ProfsTer2
NM_004360.5:c.2037del MANE Select NP_004351.1:p.Thr680ProfsTer2
NM_001317184.2:c.1854del NP_001304113.1:p.Thr619ProfsTer2
NM_001317185.2:c.489del NP_001304114.1:p.Thr164ProfsTer2
NM_001317186.2:c.72del NP_001304115.1:p.Thr25ProfsTer2