Canonical Allele Identifier: CA2633931998
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829850_68829852del , CM000678.2:g.68829850_68829852del GRCh38
NC_000016.9:g.68863753_68863755del , CM000678.1:g.68863753_68863755del GRCh37
NC_000016.8:g.67421254_67421256del NCBI36
NG_008021.1:g.97559_97561del , LRG_301:g.97559_97561del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+53_2439+55del MANE Select ENSP00000261769.4:n.2439+53_2439+55del
ENST00000261769.9:c.2439+53_2439+55del ENSP00000261769.4:n.2439+53_2439+55del
ENST00000422392.6:c.2256+53_2256+55del ENSP00000414946.2:n.2256+53_2256+55del
ENST00000562118.1:n.657+53_657+55del
ENST00000562836.5:n.2510+53_2510+55del
ENST00000566510.5:c.*1105+53_*1105+55del ENSP00000458139.1:n.*1105+53_*1105+55del
ENST00000566612.5:c.*679+53_*679+55del ENSP00000454782.1:n.*679+53_*679+55del
ENST00000611625.4:c.2502+53_2502+55del ENSP00000481063.1:n.2502+53_2502+55del
ENST00000612417.4:c.1853+3296_1853+3298del ENSP00000478360.1:n.1853+3296_1853+3298del
ENST00000621016.4:c.1866-4353_1866-4351del ENSP00000480664.1:n.1866-4353_1866-4351del
NM_004360.3:c.2439+53_2439+55del , LRG_301t1:c.2439+53_2439+55del NP_004351.1:n.2439+53_2439+55del
XM_011523488.1:c.1704+53_1704+55del XP_011521790.1:n.1704+53_1704+55del
XM_011523489.1:c.1704+53_1704+55del XP_011521791.1:n.1704+53_1704+55del
NM_001317184.1:c.2256+53_2256+55del NP_001304113.1:n.2256+53_2256+55del
NM_001317185.1:c.891+53_891+55del NP_001304114.1:n.891+53_891+55del
NM_001317186.1:c.474+53_474+55del NP_001304115.1:n.474+53_474+55del
NM_004360.4:c.2439+53_2439+55del NP_004351.1:n.2439+53_2439+55del
NM_004360.5:c.2439+53_2439+55del MANE Select NP_004351.1:n.2439+53_2439+55del
NM_001317184.2:c.2256+53_2256+55del NP_001304113.1:n.2256+53_2256+55del
NM_001317185.2:c.891+53_891+55del NP_001304114.1:n.891+53_891+55del
NM_001317186.2:c.474+53_474+55del NP_001304115.1:n.474+53_474+55del