Canonical Allele Identifier: CA656432620
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833512_68833513del , CM000678.2:g.68833512_68833513del GRCh38
NC_000016.9:g.68867415_68867416del , CM000678.1:g.68867415_68867416del GRCh37
NC_000016.8:g.67424916_67424917del NCBI36
NG_008021.1:g.101221_101222del , LRG_301:g.101221_101222del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.*13_*14del MANE Select ENSP00000261769.4:n.*13_*14del
ENST00000261769.9:c.*13_*14del ENSP00000261769.4:n.*13_*14del
ENST00000422392.6:c.*13_*14del ENSP00000414946.2:n.*13_*14del
ENST00000562118.1:n.880_881del
ENST00000562836.5:n.2733_2734del
ENST00000566510.5:c.*1328_*1329del ENSP00000458139.1:n.*1328_*1329del
ENST00000566612.5:c.*902_*903del ENSP00000454782.1:n.*902_*903del
ENST00000611625.4:c.*13_*14del ENSP00000481063.1:n.*13_*14del
ENST00000612417.4:c.1854-679_1854-678del ENSP00000478360.1:n.1854-679_1854-678del
ENST00000621016.4:c.1866-691_1866-690del ENSP00000480664.1:n.1866-691_1866-690del
NM_004360.3:c.*13_*14del , LRG_301t1:c.*13_*14del NP_004351.1:n.*13_*14del
XM_011523488.1:c.*13_*14del XP_011521790.1:n.*13_*14del
XM_011523489.1:c.*13_*14del XP_011521791.1:n.*13_*14del
NM_001317184.1:c.*13_*14del NP_001304113.1:n.*13_*14del
NM_001317185.1:c.*13_*14del NP_001304114.1:n.*13_*14del
NM_001317186.1:c.*13_*14del NP_001304115.1:n.*13_*14del
NM_004360.4:c.*13_*14del NP_004351.1:n.*13_*14del
NM_004360.5:c.*13_*14del MANE Select NP_004351.1:n.*13_*14del
NM_001317184.2:c.*13_*14del NP_001304113.1:n.*13_*14del
NM_001317185.2:c.*13_*14del NP_001304114.1:n.*13_*14del
NM_001317186.2:c.*13_*14del NP_001304115.1:n.*13_*14del