Canonical Allele Identifier: CA163542
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68823526_68823527del , CM000678.2:g.68823526_68823527del GRCh38
NC_000016.9:g.68857429_68857430del , CM000678.1:g.68857429_68857430del GRCh37
NC_000016.8:g.67414930_67414931del NCBI36
NG_008021.1:g.91235_91236del , LRG_301:g.91235_91236del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2064_2065del MANE Select ENSP00000261769.4:p.Cys688Ter
ENST00000261769.9:c.2064_2065del ENSP00000261769.4:p.Cys688Ter
ENST00000422392.6:c.1881_1882del ENSP00000414946.2:p.Cys627Ter
ENST00000562118.1:n.282_283del
ENST00000562836.5:n.2135_2136del
ENST00000566510.5:c.*730_*731del ENSP00000458139.1:n.*730_*731del
ENST00000566612.5:c.*304_*305del ENSP00000454782.1:n.*304_*305del
ENST00000611625.4:c.2127_2128del ENSP00000481063.1:p.Cys709Ter
ENST00000612417.4:c.1830+1407_1830+1408del ENSP00000478360.1:n.1830+1407_1830+1408del
ENST00000621016.4:c.1865+1372_1865+1373del ENSP00000480664.1:n.1865+1372_1865+1373del
NM_004360.3:c.2064_2065del , LRG_301t1:c.2064_2065del NP_004351.1:p.Cys688Ter
XM_011523488.1:c.1329_1330del XP_011521790.1:p.Cys443Ter
XM_011523489.1:c.1329_1330del XP_011521791.1:p.Cys443Ter
NM_001317184.1:c.1881_1882del NP_001304113.1:p.Cys627Ter
NM_001317185.1:c.516_517del NP_001304114.1:p.Cys172Ter
NM_001317186.1:c.99_100del NP_001304115.1:p.Cys33Ter
NM_004360.4:c.2064_2065del NP_004351.1:p.Cys688Ter
NM_004360.5:c.2064_2065del MANE Select NP_004351.1:p.Cys688Ter
NM_001317184.2:c.1881_1882del NP_001304113.1:p.Cys627Ter
NM_001317185.2:c.516_517del NP_001304114.1:p.Cys172Ter
NM_001317186.2:c.99_100del NP_001304115.1:p.Cys33Ter