Canonical Allele Identifier: CA2580612864
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1760399
ClinVar RCV Id: RCV002400775 RCV003099731
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68810283_68810285del , CM000678.2:g.68810283_68810285del GRCh38
NC_000016.9:g.68844186_68844188del , CM000678.1:g.68844186_68844188del GRCh37
NC_000016.8:g.67401687_67401689del NCBI36
NG_008021.1:g.77992_77994del , LRG_301:g.77992_77994del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.774_776del MANE Select ENSP00000261769.4:p.Asn258del
ENST00000261769.9:c.774_776del ENSP00000261769.4:p.Asn258del
ENST00000422392.6:c.774_776del ENSP00000414946.2:p.Asn258del
ENST00000561751.1:c.455-1401_455-1399del
ENST00000562836.5:n.845_847del
ENST00000566510.5:c.618_620del ENSP00000458139.1:p.Asn206del
ENST00000566612.5:c.774_776del ENSP00000454782.1:p.Asn258del
ENST00000611625.4:c.774_776del ENSP00000481063.1:p.Asn258del
ENST00000612417.4:c.774_776del ENSP00000478360.1:p.Asn258del
ENST00000621016.4:c.774_776del ENSP00000480664.1:p.Asn258del
NM_004360.3:c.774_776del , LRG_301t1:c.774_776del NP_004351.1:p.Asn258del
XM_011523488.1:c.39_41del XP_011521790.1:p.Asn13del
XM_011523489.1:c.39_41del XP_011521791.1:p.Asn13del
NM_001317184.1:c.774_776del NP_001304113.1:p.Asn258del
NM_001317185.1:c.-842_-840del NP_001304114.1:n.-842_-840del
NM_001317186.1:c.-1046_-1044del NP_001304115.1:n.-1046_-1044del
NM_004360.4:c.774_776del NP_004351.1:p.Asn258del
NM_004360.5:c.774_776del MANE Select NP_004351.1:p.Asn258del
NM_001317184.2:c.774_776del NP_001304113.1:p.Asn258del
NM_001317185.2:c.-842_-840del NP_001304114.1:n.-842_-840del
NM_001317186.2:c.-1046_-1044del NP_001304115.1:n.-1046_-1044del
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