Canonical Allele Identifier: CA2807471200
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68801846_68801847del , CM000678.2:g.68801846_68801847del GRCh38
NC_000016.9:g.68835749_68835750del , CM000678.1:g.68835749_68835750del GRCh37
NC_000016.8:g.67393250_67393251del NCBI36
NG_008021.1:g.69555_69556del , LRG_301:g.69555_69556del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.340_341del MANE Select ENSP00000261769.4:p.Val114HisfsTer?
ENST00000261769.9:c.340_341del ENSP00000261769.4:p.Val114HisfsTer?
ENST00000422392.6:c.340_341del ENSP00000414946.2:p.Val114HisfsTer?
ENST00000561751.1:c.107_108del
ENST00000562836.5:n.411_412del
ENST00000564676.5:n.622_623del
ENST00000564745.1:n.335_336del
ENST00000566510.5:c.340_341del ENSP00000458139.1:p.Val114HisfsTer?
ENST00000566612.5:c.340_341del ENSP00000454782.1:p.Val114HisfsTer?
ENST00000611625.4:c.340_341del ENSP00000481063.1:p.Val114HisfsTer?
ENST00000612417.4:c.340_341del ENSP00000478360.1:p.Val114HisfsTer?
ENST00000621016.4:c.340_341del ENSP00000480664.1:p.Val114HisfsTer?
NM_004360.3:c.340_341del , LRG_301t1:c.340_341del NP_004351.1:p.Val114HisfsTer?
XM_011523488.1:c.-396_-395del XP_011521790.1:n.-396_-395del
XM_011523489.1:c.-396_-395del XP_011521791.1:n.-396_-395del
NM_001317184.1:c.340_341del NP_001304113.1:p.Val114HisfsTer?
NM_001317185.1:c.-1276_-1275del NP_001304114.1:n.-1276_-1275del
NM_001317186.1:c.-1480_-1479del NP_001304115.1:n.-1480_-1479del
NM_004360.4:c.340_341del NP_004351.1:p.Val114HisfsTer?
NM_004360.5:c.340_341del MANE Select NP_004351.1:p.Val114HisfsTer?
NM_001317184.2:c.340_341del NP_001304113.1:p.Val114HisfsTer?
NM_001317185.2:c.-1276_-1275del NP_001304114.1:n.-1276_-1275del
NM_001317186.2:c.-1480_-1479del NP_001304115.1:n.-1480_-1479del