Canonical Allele Identifier: CA2633932084
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829936_68829951del , CM000678.2:g.68829936_68829951del GRCh38
NC_000016.9:g.68863839_68863854del , CM000678.1:g.68863839_68863854del GRCh37
NC_000016.8:g.67421340_67421355del NCBI36
NG_008021.1:g.97645_97660del , LRG_301:g.97645_97660del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+139_2439+154del MANE Select ENSP00000261769.4:n.2439+139_2439+154del
ENST00000261769.9:c.2439+139_2439+154del ENSP00000261769.4:n.2439+139_2439+154del
ENST00000422392.6:c.2256+139_2256+154del ENSP00000414946.2:n.2256+139_2256+154del
ENST00000562118.1:n.657+139_657+154del
ENST00000562836.5:n.2510+139_2510+154del
ENST00000566510.5:c.*1105+139_*1105+154del ENSP00000458139.1:n.*1105+139_*1105+154del
ENST00000566612.5:c.*679+139_*679+154del ENSP00000454782.1:n.*679+139_*679+154del
ENST00000611625.4:c.2502+139_2502+154del ENSP00000481063.1:n.2502+139_2502+154del
ENST00000612417.4:c.1853+3382_1853+3397del ENSP00000478360.1:n.1853+3382_1853+3397del
ENST00000621016.4:c.1866-4267_1866-4252del ENSP00000480664.1:n.1866-4267_1866-4252del
NM_004360.3:c.2439+139_2439+154del , LRG_301t1:c.2439+139_2439+154del NP_004351.1:n.2439+139_2439+154del
XM_011523488.1:c.1704+139_1704+154del XP_011521790.1:n.1704+139_1704+154del
XM_011523489.1:c.1704+139_1704+154del XP_011521791.1:n.1704+139_1704+154del
NM_001317184.1:c.2256+139_2256+154del NP_001304113.1:n.2256+139_2256+154del
NM_001317185.1:c.891+139_891+154del NP_001304114.1:n.891+139_891+154del
NM_001317186.1:c.474+139_474+154del NP_001304115.1:n.474+139_474+154del
NM_004360.4:c.2439+139_2439+154del NP_004351.1:n.2439+139_2439+154del
NM_004360.5:c.2439+139_2439+154del MANE Select NP_004351.1:n.2439+139_2439+154del
NM_001317184.2:c.2256+139_2256+154del NP_001304113.1:n.2256+139_2256+154del
NM_001317185.2:c.891+139_891+154del NP_001304114.1:n.891+139_891+154del
NM_001317186.2:c.474+139_474+154del NP_001304115.1:n.474+139_474+154del