Canonical Allele Identifier: CA623137602
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1567516310

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829953_68829957del , CM000678.2:g.68829953_68829957del GRCh38
NC_000016.9:g.68863856_68863860del , CM000678.1:g.68863856_68863860del GRCh37
NC_000016.8:g.67421357_67421361del NCBI36
NG_008021.1:g.97662_97666del , LRG_301:g.97662_97666del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+156_2439+160del MANE Select ENSP00000261769.4:n.2439+156_2439+160del
ENST00000261769.9:c.2439+156_2439+160del ENSP00000261769.4:n.2439+156_2439+160del
ENST00000422392.6:c.2256+156_2256+160del ENSP00000414946.2:n.2256+156_2256+160del
ENST00000562118.1:n.657+156_657+160del
ENST00000562836.5:n.2510+156_2510+160del
ENST00000566510.5:c.*1105+156_*1105+160del ENSP00000458139.1:n.*1105+156_*1105+160del
ENST00000566612.5:c.*679+156_*679+160del ENSP00000454782.1:n.*679+156_*679+160del
ENST00000611625.4:c.2502+156_2502+160del ENSP00000481063.1:n.2502+156_2502+160del
ENST00000612417.4:c.1853+3399_1853+3403del ENSP00000478360.1:n.1853+3399_1853+3403del
ENST00000621016.4:c.1866-4250_1866-4246del ENSP00000480664.1:n.1866-4250_1866-4246del
NM_004360.3:c.2439+156_2439+160del , LRG_301t1:c.2439+156_2439+160del NP_004351.1:n.2439+156_2439+160del
XM_011523488.1:c.1704+156_1704+160del XP_011521790.1:n.1704+156_1704+160del
XM_011523489.1:c.1704+156_1704+160del XP_011521791.1:n.1704+156_1704+160del
NM_001317184.1:c.2256+156_2256+160del NP_001304113.1:n.2256+156_2256+160del
NM_001317185.1:c.891+156_891+160del NP_001304114.1:n.891+156_891+160del
NM_001317186.1:c.474+156_474+160del NP_001304115.1:n.474+156_474+160del
NM_004360.4:c.2439+156_2439+160del NP_004351.1:n.2439+156_2439+160del
NM_004360.5:c.2439+156_2439+160del MANE Select NP_004351.1:n.2439+156_2439+160del
NM_001317184.2:c.2256+156_2256+160del NP_001304113.1:n.2256+156_2256+160del
NM_001317185.2:c.891+156_891+160del NP_001304114.1:n.891+156_891+160del
NM_001317186.2:c.474+156_474+160del NP_001304115.1:n.474+156_474+160del