Canonical Allele Identifier: CA2580617411
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68823440del , CM000678.2:g.68823440del GRCh38
NC_000016.9:g.68857343del , CM000678.1:g.68857343del GRCh37
NC_000016.8:g.67414844del NCBI36
NG_008021.1:g.91149del , LRG_301:g.91149del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1978del MANE Select ENSP00000261769.4:p.Val660TrpfsTer19
ENST00000261769.9:c.1978del ENSP00000261769.4:p.Val660TrpfsTer19
ENST00000422392.6:c.1795del ENSP00000414946.2:p.Val599TrpfsTer19
ENST00000562118.1:n.196del
ENST00000562836.5:n.2049del
ENST00000566510.5:c.*644del ENSP00000458139.1:n.*644del
ENST00000566612.5:c.*218del ENSP00000454782.1:n.*218del
ENST00000611625.4:c.2041del ENSP00000481063.1:p.Val681TrpfsTer19
ENST00000612417.4:c.1830+1321del ENSP00000478360.1:n.1830+1321del
ENST00000621016.4:c.1865+1286del ENSP00000480664.1:n.1865+1286del
NM_004360.3:c.1978del , LRG_301t1:c.1978del NP_004351.1:p.Val660TrpfsTer19
XM_011523488.1:c.1243del XP_011521790.1:p.Val415TrpfsTer19
XM_011523489.1:c.1243del XP_011521791.1:p.Val415TrpfsTer19
NM_001317184.1:c.1795del NP_001304113.1:p.Val599TrpfsTer19
NM_001317185.1:c.430del NP_001304114.1:p.Val144TrpfsTer19
NM_001317186.1:c.13del NP_001304115.1:p.Val5TrpfsTer19
NM_004360.4:c.1978del NP_004351.1:p.Val660TrpfsTer19
NM_004360.5:c.1978del MANE Select NP_004351.1:p.Val660TrpfsTer19
NM_001317184.2:c.1795del NP_001304113.1:p.Val599TrpfsTer19
NM_001317185.2:c.430del NP_001304114.1:p.Val144TrpfsTer19
NM_001317186.2:c.13del NP_001304115.1:p.Val5TrpfsTer19