Canonical Allele Identifier: CA891842213
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819409del , CM000678.2:g.68819409del GRCh38
NC_000016.9:g.68853312del , CM000678.1:g.68853312del GRCh37
NC_000016.8:g.67410813del NCBI36
NG_008021.1:g.87118del , LRG_301:g.87118del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1695del MANE Select ENSP00000261769.4:p.Ile566Ter
ENST00000261769.9:c.1695del ENSP00000261769.4:p.Ile566Ter
ENST00000422392.6:c.1512del ENSP00000414946.2:p.Ile505Ter
ENST00000562836.5:n.1766del
ENST00000566510.5:c.*361del ENSP00000458139.1:n.*361del
ENST00000566612.5:c.1566-2592del ENSP00000454782.1:n.1566-2592del
ENST00000611625.4:c.1758del ENSP00000481063.1:p.Ile587Ter
ENST00000612417.4:c.1695del ENSP00000478360.1:p.Ile566Ter
ENST00000621016.4:c.1695del ENSP00000480664.1:p.Ile566Ter
NM_004360.3:c.1695del , LRG_301t1:c.1695del NP_004351.1:p.Ile566Ter
XM_011523488.1:c.960del XP_011521790.1:p.Ile321Ter
XM_011523489.1:c.960del XP_011521791.1:p.Ile321Ter
NM_001317184.1:c.1512del NP_001304113.1:p.Ile505Ter
NM_001317185.1:c.147del NP_001304114.1:p.Ile50Ter
NM_001317186.1:c.-254-2592del NP_001304115.1:n.-254-2592del
NM_004360.4:c.1695del NP_004351.1:p.Ile566Ter
NM_004360.5:c.1695del MANE Select NP_004351.1:p.Ile566Ter
NM_001317184.2:c.1512del NP_001304113.1:p.Ile505Ter
NM_001317185.2:c.147del NP_001304114.1:p.Ile50Ter
NM_001317186.2:c.-254-2592del NP_001304115.1:n.-254-2592del