Canonical Allele Identifier: CA978527735
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1961443349

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829977_68829978del , CM000678.2:g.68829977_68829978del GRCh38
NC_000016.9:g.68863880_68863881del , CM000678.1:g.68863880_68863881del GRCh37
NC_000016.8:g.67421381_67421382del NCBI36
NG_008021.1:g.97686_97687del , LRG_301:g.97686_97687del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+180_2439+181del MANE Select ENSP00000261769.4:n.2439+180_2439+181del
ENST00000261769.9:c.2439+180_2439+181del ENSP00000261769.4:n.2439+180_2439+181del
ENST00000422392.6:c.2256+180_2256+181del ENSP00000414946.2:n.2256+180_2256+181del
ENST00000562118.1:n.657+180_657+181del
ENST00000562836.5:n.2510+180_2510+181del
ENST00000566510.5:c.*1105+180_*1105+181del ENSP00000458139.1:n.*1105+180_*1105+181del
ENST00000566612.5:c.*679+180_*679+181del ENSP00000454782.1:n.*679+180_*679+181del
ENST00000611625.4:c.2502+180_2502+181del ENSP00000481063.1:n.2502+180_2502+181del
ENST00000612417.4:c.1853+3423_1853+3424del ENSP00000478360.1:n.1853+3423_1853+3424del
ENST00000621016.4:c.1866-4226_1866-4225del ENSP00000480664.1:n.1866-4226_1866-4225del
NM_004360.3:c.2439+180_2439+181del , LRG_301t1:c.2439+180_2439+181del NP_004351.1:n.2439+180_2439+181del
XM_011523488.1:c.1704+180_1704+181del XP_011521790.1:n.1704+180_1704+181del
XM_011523489.1:c.1704+180_1704+181del XP_011521791.1:n.1704+180_1704+181del
NM_001317184.1:c.2256+180_2256+181del NP_001304113.1:n.2256+180_2256+181del
NM_001317185.1:c.891+180_891+181del NP_001304114.1:n.891+180_891+181del
NM_001317186.1:c.474+180_474+181del NP_001304115.1:n.474+180_474+181del
NM_004360.4:c.2439+180_2439+181del NP_004351.1:n.2439+180_2439+181del
NM_004360.5:c.2439+180_2439+181del MANE Select NP_004351.1:n.2439+180_2439+181del
NM_001317184.2:c.2256+180_2256+181del NP_001304113.1:n.2256+180_2256+181del
NM_001317185.2:c.891+180_891+181del NP_001304114.1:n.891+180_891+181del
NM_001317186.2:c.474+180_474+181del NP_001304115.1:n.474+180_474+181del