Canonical Allele Identifier: CA723137340
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1427621489

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819958_68819961del , CM000678.2:g.68819958_68819961del GRCh38
NC_000016.9:g.68853861_68853864del , CM000678.1:g.68853861_68853864del GRCh37
NC_000016.8:g.67411362_67411365del NCBI36
NG_008021.1:g.87667_87670del , LRG_301:g.87667_87670del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1711+533_1711+536del MANE Select ENSP00000261769.4:n.1711+533_1711+536del
ENST00000261769.9:c.1711+533_1711+536del ENSP00000261769.4:n.1711+533_1711+536del
ENST00000422392.6:c.1528+533_1528+536del ENSP00000414946.2:n.1528+533_1528+536del
ENST00000562836.5:n.1782+533_1782+536del
ENST00000566510.5:c.*377+533_*377+536del ENSP00000458139.1:n.*377+533_*377+536del
ENST00000566612.5:c.1566-2043_1566-2040del ENSP00000454782.1:n.1566-2043_1566-2040del
ENST00000611625.4:c.1774+533_1774+536del ENSP00000481063.1:n.1774+533_1774+536del
ENST00000612417.4:c.1711+533_1711+536del ENSP00000478360.1:n.1711+533_1711+536del
ENST00000621016.4:c.1711+533_1711+536del ENSP00000480664.1:n.1711+533_1711+536del
NM_004360.3:c.1711+533_1711+536del , LRG_301t1:c.1711+533_1711+536del NP_004351.1:n.1711+533_1711+536del
XM_011523488.1:c.976+533_976+536del XP_011521790.1:n.976+533_976+536del
XM_011523489.1:c.976+533_976+536del XP_011521791.1:n.976+533_976+536del
NM_001317184.1:c.1528+533_1528+536del NP_001304113.1:n.1528+533_1528+536del
NM_001317185.1:c.163+533_163+536del NP_001304114.1:n.163+533_163+536del
NM_001317186.1:c.-254-2043_-254-2040del NP_001304115.1:n.-254-2043_-254-2040del
NM_004360.4:c.1711+533_1711+536del NP_004351.1:n.1711+533_1711+536del
NM_004360.5:c.1711+533_1711+536del MANE Select NP_004351.1:n.1711+533_1711+536del
NM_001317184.2:c.1528+533_1528+536del NP_001304113.1:n.1528+533_1528+536del
NM_001317185.2:c.163+533_163+536del NP_001304114.1:n.163+533_163+536del
NM_001317186.2:c.-254-2043_-254-2040del NP_001304115.1:n.-254-2043_-254-2040del