Canonical Allele Identifier: CA978527538
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829953_68829970del , CM000678.2:g.68829953_68829970del GRCh38
NC_000016.9:g.68863856_68863873del , CM000678.1:g.68863856_68863873del GRCh37
NC_000016.8:g.67421357_67421374del NCBI36
NG_008021.1:g.97662_97679del , LRG_301:g.97662_97679del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+156_2439+173del MANE Select ENSP00000261769.4:n.2439+156_2439+173del
ENST00000261769.9:c.2439+156_2439+173del ENSP00000261769.4:n.2439+156_2439+173del
ENST00000422392.6:c.2256+156_2256+173del ENSP00000414946.2:n.2256+156_2256+173del
ENST00000562118.1:n.657+156_657+173del
ENST00000562836.5:n.2510+156_2510+173del
ENST00000566510.5:c.*1105+156_*1105+173del ENSP00000458139.1:n.*1105+156_*1105+173del
ENST00000566612.5:c.*679+156_*679+173del ENSP00000454782.1:n.*679+156_*679+173del
ENST00000611625.4:c.2502+156_2502+173del ENSP00000481063.1:n.2502+156_2502+173del
ENST00000612417.4:c.1853+3399_1853+3416del ENSP00000478360.1:n.1853+3399_1853+3416del
ENST00000621016.4:c.1866-4250_1866-4233del ENSP00000480664.1:n.1866-4250_1866-4233del
NM_004360.3:c.2439+156_2439+173del , LRG_301t1:c.2439+156_2439+173del NP_004351.1:n.2439+156_2439+173del
XM_011523488.1:c.1704+156_1704+173del XP_011521790.1:n.1704+156_1704+173del
XM_011523489.1:c.1704+156_1704+173del XP_011521791.1:n.1704+156_1704+173del
NM_001317184.1:c.2256+156_2256+173del NP_001304113.1:n.2256+156_2256+173del
NM_001317185.1:c.891+156_891+173del NP_001304114.1:n.891+156_891+173del
NM_001317186.1:c.474+156_474+173del NP_001304115.1:n.474+156_474+173del
NM_004360.4:c.2439+156_2439+173del NP_004351.1:n.2439+156_2439+173del
NM_004360.5:c.2439+156_2439+173del MANE Select NP_004351.1:n.2439+156_2439+173del
NM_001317184.2:c.2256+156_2256+173del NP_001304113.1:n.2256+156_2256+173del
NM_001317185.2:c.891+156_891+173del NP_001304114.1:n.891+156_891+173del
NM_001317186.2:c.474+156_474+173del NP_001304115.1:n.474+156_474+173del