Canonical Allele Identifier: CA2581463427
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833311del , CM000678.2:g.68833311del GRCh38
NC_000016.9:g.68867214del , CM000678.1:g.68867214del GRCh37
NC_000016.8:g.67424715del NCBI36
NG_008021.1:g.101020del , LRG_301:g.101020del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2461del MANE Select ENSP00000261769.4:p.Asp821ThrfsTer25
ENST00000261769.9:c.2461del ENSP00000261769.4:p.Asp821ThrfsTer25
ENST00000422392.6:c.2278del ENSP00000414946.2:p.Asp760ThrfsTer25
ENST00000562118.1:n.679del
ENST00000562836.5:n.2532del
ENST00000566510.5:c.*1127del ENSP00000458139.1:n.*1127del
ENST00000566612.5:c.*701del ENSP00000454782.1:n.*701del
ENST00000611625.4:c.2524del ENSP00000481063.1:p.Asp842ThrfsTer25
ENST00000612417.4:c.1854-880del ENSP00000478360.1:n.1854-880del
ENST00000621016.4:c.1866-892del ENSP00000480664.1:n.1866-892del
NM_004360.3:c.2461del , LRG_301t1:c.2461del NP_004351.1:p.Asp821ThrfsTer25
XM_011523488.1:c.1726del XP_011521790.1:p.Asp576ThrfsTer25
XM_011523489.1:c.1726del XP_011521791.1:p.Asp576ThrfsTer25
NM_001317184.1:c.2278del NP_001304113.1:p.Asp760ThrfsTer25
NM_001317185.1:c.913del NP_001304114.1:p.Asp305ThrfsTer25
NM_001317186.1:c.496del NP_001304115.1:p.Asp166ThrfsTer25
NM_004360.4:c.2461del NP_004351.1:p.Asp821ThrfsTer25
NM_004360.5:c.2461del MANE Select NP_004351.1:p.Asp821ThrfsTer25
NM_001317184.2:c.2278del NP_001304113.1:p.Asp760ThrfsTer25
NM_001317185.2:c.913del NP_001304114.1:p.Asp305ThrfsTer25
NM_001317186.2:c.496del NP_001304115.1:p.Asp166ThrfsTer25