Canonical Allele Identifier: CA2633932102
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829948_68829958del , CM000678.2:g.68829948_68829958del GRCh38
NC_000016.9:g.68863851_68863861del , CM000678.1:g.68863851_68863861del GRCh37
NC_000016.8:g.67421352_67421362del NCBI36
NG_008021.1:g.97657_97667del , LRG_301:g.97657_97667del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+151_2439+161del MANE Select ENSP00000261769.4:n.2439+151_2439+161del
ENST00000261769.9:c.2439+151_2439+161del ENSP00000261769.4:n.2439+151_2439+161del
ENST00000422392.6:c.2256+151_2256+161del ENSP00000414946.2:n.2256+151_2256+161del
ENST00000562118.1:n.657+151_657+161del
ENST00000562836.5:n.2510+151_2510+161del
ENST00000566510.5:c.*1105+151_*1105+161del ENSP00000458139.1:n.*1105+151_*1105+161del
ENST00000566612.5:c.*679+151_*679+161del ENSP00000454782.1:n.*679+151_*679+161del
ENST00000611625.4:c.2502+151_2502+161del ENSP00000481063.1:n.2502+151_2502+161del
ENST00000612417.4:c.1853+3394_1853+3404del ENSP00000478360.1:n.1853+3394_1853+3404del
ENST00000621016.4:c.1866-4255_1866-4245del ENSP00000480664.1:n.1866-4255_1866-4245del
NM_004360.3:c.2439+151_2439+161del , LRG_301t1:c.2439+151_2439+161del NP_004351.1:n.2439+151_2439+161del
XM_011523488.1:c.1704+151_1704+161del XP_011521790.1:n.1704+151_1704+161del
XM_011523489.1:c.1704+151_1704+161del XP_011521791.1:n.1704+151_1704+161del
NM_001317184.1:c.2256+151_2256+161del NP_001304113.1:n.2256+151_2256+161del
NM_001317185.1:c.891+151_891+161del NP_001304114.1:n.891+151_891+161del
NM_001317186.1:c.474+151_474+161del NP_001304115.1:n.474+151_474+161del
NM_004360.4:c.2439+151_2439+161del NP_004351.1:n.2439+151_2439+161del
NM_004360.5:c.2439+151_2439+161del MANE Select NP_004351.1:n.2439+151_2439+161del
NM_001317184.2:c.2256+151_2256+161del NP_001304113.1:n.2256+151_2256+161del
NM_001317185.2:c.891+151_891+161del NP_001304114.1:n.891+151_891+161del
NM_001317186.2:c.474+151_474+161del NP_001304115.1:n.474+151_474+161del