Canonical Allele Identifier: CA623137630
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1776769203

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829976_68829983del , CM000678.2:g.68829976_68829983del GRCh38
NC_000016.9:g.68863879_68863886del , CM000678.1:g.68863879_68863886del GRCh37
NC_000016.8:g.67421380_67421387del NCBI36
NG_008021.1:g.97685_97692del , LRG_301:g.97685_97692del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+179_2439+186del MANE Select ENSP00000261769.4:n.2439+179_2439+186del
ENST00000261769.9:c.2439+179_2439+186del ENSP00000261769.4:n.2439+179_2439+186del
ENST00000422392.6:c.2256+179_2256+186del ENSP00000414946.2:n.2256+179_2256+186del
ENST00000562118.1:n.657+179_657+186del
ENST00000562836.5:n.2510+179_2510+186del
ENST00000566510.5:c.*1105+179_*1105+186del ENSP00000458139.1:n.*1105+179_*1105+186del
ENST00000566612.5:c.*679+179_*679+186del ENSP00000454782.1:n.*679+179_*679+186del
ENST00000611625.4:c.2502+179_2502+186del ENSP00000481063.1:n.2502+179_2502+186del
ENST00000612417.4:c.1853+3422_1853+3429del ENSP00000478360.1:n.1853+3422_1853+3429del
ENST00000621016.4:c.1866-4227_1866-4220del ENSP00000480664.1:n.1866-4227_1866-4220del
NM_004360.3:c.2439+179_2439+186del , LRG_301t1:c.2439+179_2439+186del NP_004351.1:n.2439+179_2439+186del
XM_011523488.1:c.1704+179_1704+186del XP_011521790.1:n.1704+179_1704+186del
XM_011523489.1:c.1704+179_1704+186del XP_011521791.1:n.1704+179_1704+186del
NM_001317184.1:c.2256+179_2256+186del NP_001304113.1:n.2256+179_2256+186del
NM_001317185.1:c.891+179_891+186del NP_001304114.1:n.891+179_891+186del
NM_001317186.1:c.474+179_474+186del NP_001304115.1:n.474+179_474+186del
NM_004360.4:c.2439+179_2439+186del NP_004351.1:n.2439+179_2439+186del
NM_004360.5:c.2439+179_2439+186del MANE Select NP_004351.1:n.2439+179_2439+186del
NM_001317184.2:c.2256+179_2256+186del NP_001304113.1:n.2256+179_2256+186del
NM_001317185.2:c.891+179_891+186del NP_001304114.1:n.891+179_891+186del
NM_001317186.2:c.474+179_474+186del NP_001304115.1:n.474+179_474+186del