Canonical Allele Identifier: CA2576038979
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833569del , CM000678.2:g.68833569del GRCh38
NC_000016.9:g.68867472del , CM000678.1:g.68867472del GRCh37
NC_000016.8:g.67424973del NCBI36
NG_008021.1:g.101278del , LRG_301:g.101278del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.*70del MANE Select ENSP00000261769.4:n.*70del
ENST00000261769.9:c.*70del ENSP00000261769.4:n.*70del
ENST00000562118.1:n.937del
ENST00000566612.5:c.*959del ENSP00000454782.1:n.*959del
ENST00000611625.4:c.*70del ENSP00000481063.1:n.*70del
ENST00000612417.4:c.1854-622del ENSP00000478360.1:n.1854-622del
ENST00000621016.4:c.1866-634del ENSP00000480664.1:n.1866-634del
NM_004360.3:c.*70del , LRG_301t1:c.*70del NP_004351.1:n.*70del
XM_011523488.1:c.*70del XP_011521790.1:n.*70del
XM_011523489.1:c.*70del XP_011521791.1:n.*70del
NM_001317184.1:c.*70del NP_001304113.1:n.*70del
NM_001317185.1:c.*70del NP_001304114.1:n.*70del
NM_001317186.1:c.*70del NP_001304115.1:n.*70del
NM_004360.4:c.*70del NP_004351.1:n.*70del
NM_004360.5:c.*70del MANE Select NP_004351.1:n.*70del
NM_001317184.2:c.*70del NP_001304113.1:n.*70del
NM_001317185.2:c.*70del NP_001304114.1:n.*70del
NM_001317186.2:c.*70del NP_001304115.1:n.*70del