Canonical Allele Identifier: CA978522065
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1961058118

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68818864_68818874del , CM000678.2:g.68818864_68818874del GRCh38
NC_000016.9:g.68852767_68852777del , CM000678.1:g.68852767_68852777del GRCh37
NC_000016.8:g.67410268_67410278del NCBI36
NG_008021.1:g.86573_86583del , LRG_301:g.86573_86583del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1566-416_1566-406del MANE Select ENSP00000261769.4:n.1566-416_1566-406del
ENST00000261769.9:c.1566-416_1566-406del ENSP00000261769.4:n.1566-416_1566-406del
ENST00000422392.6:c.1383-416_1383-406del ENSP00000414946.2:n.1383-416_1383-406del
ENST00000562836.5:n.1637-416_1637-406del
ENST00000566510.5:c.*232-416_*232-406del ENSP00000458139.1:n.*232-416_*232-406del
ENST00000566612.5:c.1565+3105_1565+3115del ENSP00000454782.1:n.1565+3105_1565+3115del
ENST00000611625.4:c.1629-416_1629-406del ENSP00000481063.1:n.1629-416_1629-406del
ENST00000612417.4:c.1566-416_1566-406del ENSP00000478360.1:n.1566-416_1566-406del
ENST00000621016.4:c.1566-416_1566-406del ENSP00000480664.1:n.1566-416_1566-406del
NM_004360.3:c.1566-416_1566-406del , LRG_301t1:c.1566-416_1566-406del NP_004351.1:n.1566-416_1566-406del
XM_011523488.1:c.831-416_831-406del XP_011521790.1:n.831-416_831-406del
XM_011523489.1:c.831-416_831-406del XP_011521791.1:n.831-416_831-406del
NM_001317184.1:c.1383-416_1383-406del NP_001304113.1:n.1383-416_1383-406del
NM_001317185.1:c.18-416_18-406del NP_001304114.1:n.18-416_18-406del
NM_001317186.1:c.-255+3105_-255+3115del NP_001304115.1:n.-255+3105_-255+3115del
NM_004360.4:c.1566-416_1566-406del NP_004351.1:n.1566-416_1566-406del
NM_004360.5:c.1566-416_1566-406del MANE Select NP_004351.1:n.1566-416_1566-406del
NM_001317184.2:c.1383-416_1383-406del NP_001304113.1:n.1383-416_1383-406del
NM_001317185.2:c.18-416_18-406del NP_001304114.1:n.18-416_18-406del
NM_001317186.2:c.-255+3105_-255+3115del NP_001304115.1:n.-255+3105_-255+3115del