Canonical Allele Identifier: CA2573152517
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1437379
ClinVar RCV Id: RCV001955480
dbSNP Id: rs2152114347
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68738308del , CM000678.2:g.68738308del GRCh38
NC_000016.9:g.68772211del , CM000678.1:g.68772211del GRCh37
NC_000016.8:g.67329712del NCBI36
NG_008021.1:g.6017del , LRG_301:g.6017del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.60del MANE Select ENSP00000261769.4:p.Trp20CysfsTer?
ENST00000261769.9:c.60del ENSP00000261769.4:p.Trp20CysfsTer?
ENST00000422392.6:c.60del ENSP00000414946.2:p.Trp20CysfsTer?
ENST00000566510.5:c.60del ENSP00000458139.1:p.Trp20CysfsTer?
ENST00000566612.5:c.60del ENSP00000454782.1:p.Trp20CysfsTer?
ENST00000611625.4:c.60del ENSP00000481063.1:p.Trp20CysfsTer?
ENST00000612417.4:c.60del ENSP00000478360.1:p.Trp20CysfsTer?
ENST00000621016.4:c.60del ENSP00000480664.1:p.Trp20CysfsTer?
NM_004360.3:c.60del , LRG_301t1:c.60del NP_004351.1:p.Trp20CysfsTer?
NM_001317184.1:c.60del NP_001304113.1:p.Trp20CysfsTer?
NM_001317185.1:c.-1556del NP_001304114.1:n.-1556del
NM_001317186.1:c.-1760del NP_001304115.1:n.-1760del
NM_004360.4:c.60del NP_004351.1:p.Trp20CysfsTer?
NM_004360.5:c.60del MANE Select NP_004351.1:p.Trp20CysfsTer?
NM_001317184.2:c.60del NP_001304113.1:p.Trp20CysfsTer?
NM_001317185.2:c.-1556del NP_001304114.1:n.-1556del
NM_001317186.2:c.-1760del NP_001304115.1:n.-1760del
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