Canonical Allele Identifier: CA2807472705
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829959_68829969del , CM000678.2:g.68829959_68829969del GRCh38
NC_000016.9:g.68863862_68863872del , CM000678.1:g.68863862_68863872del GRCh37
NC_000016.8:g.67421363_67421373del NCBI36
NG_008021.1:g.97668_97678del , LRG_301:g.97668_97678del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+162_2439+172del MANE Select ENSP00000261769.4:n.2439+162_2439+172del
ENST00000261769.9:c.2439+162_2439+172del ENSP00000261769.4:n.2439+162_2439+172del
ENST00000422392.6:c.2256+162_2256+172del ENSP00000414946.2:n.2256+162_2256+172del
ENST00000562118.1:n.657+162_657+172del
ENST00000562836.5:n.2510+162_2510+172del
ENST00000566510.5:c.*1105+162_*1105+172del ENSP00000458139.1:n.*1105+162_*1105+172del
ENST00000566612.5:c.*679+162_*679+172del ENSP00000454782.1:n.*679+162_*679+172del
ENST00000611625.4:c.2502+162_2502+172del ENSP00000481063.1:n.2502+162_2502+172del
ENST00000612417.4:c.1853+3405_1853+3415del ENSP00000478360.1:n.1853+3405_1853+3415del
ENST00000621016.4:c.1866-4244_1866-4234del ENSP00000480664.1:n.1866-4244_1866-4234del
NM_004360.3:c.2439+162_2439+172del , LRG_301t1:c.2439+162_2439+172del NP_004351.1:n.2439+162_2439+172del
XM_011523488.1:c.1704+162_1704+172del XP_011521790.1:n.1704+162_1704+172del
XM_011523489.1:c.1704+162_1704+172del XP_011521791.1:n.1704+162_1704+172del
NM_001317184.1:c.2256+162_2256+172del NP_001304113.1:n.2256+162_2256+172del
NM_001317185.1:c.891+162_891+172del NP_001304114.1:n.891+162_891+172del
NM_001317186.1:c.474+162_474+172del NP_001304115.1:n.474+162_474+172del
NM_004360.4:c.2439+162_2439+172del NP_004351.1:n.2439+162_2439+172del
NM_004360.5:c.2439+162_2439+172del MANE Select NP_004351.1:n.2439+162_2439+172del
NM_001317184.2:c.2256+162_2256+172del NP_001304113.1:n.2256+162_2256+172del
NM_001317185.2:c.891+162_891+172del NP_001304114.1:n.891+162_891+172del
NM_001317186.2:c.474+162_474+172del NP_001304115.1:n.474+162_474+172del