Canonical Allele Identifier: CA723144030
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1474694357

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829875_68829876del , CM000678.2:g.68829875_68829876del GRCh38
NC_000016.9:g.68863778_68863779del , CM000678.1:g.68863778_68863779del GRCh37
NC_000016.8:g.67421279_67421280del NCBI36
NG_008021.1:g.97584_97585del , LRG_301:g.97584_97585del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+78_2439+79del MANE Select ENSP00000261769.4:n.2439+78_2439+79del
ENST00000261769.9:c.2439+78_2439+79del ENSP00000261769.4:n.2439+78_2439+79del
ENST00000422392.6:c.2256+78_2256+79del ENSP00000414946.2:n.2256+78_2256+79del
ENST00000562118.1:n.657+78_657+79del
ENST00000562836.5:n.2510+78_2510+79del
ENST00000566510.5:c.*1105+78_*1105+79del ENSP00000458139.1:n.*1105+78_*1105+79del
ENST00000566612.5:c.*679+78_*679+79del ENSP00000454782.1:n.*679+78_*679+79del
ENST00000611625.4:c.2502+78_2502+79del ENSP00000481063.1:n.2502+78_2502+79del
ENST00000612417.4:c.1853+3321_1853+3322del ENSP00000478360.1:n.1853+3321_1853+3322del
ENST00000621016.4:c.1866-4328_1866-4327del ENSP00000480664.1:n.1866-4328_1866-4327del
NM_004360.3:c.2439+78_2439+79del , LRG_301t1:c.2439+78_2439+79del NP_004351.1:n.2439+78_2439+79del
XM_011523488.1:c.1704+78_1704+79del XP_011521790.1:n.1704+78_1704+79del
XM_011523489.1:c.1704+78_1704+79del XP_011521791.1:n.1704+78_1704+79del
NM_001317184.1:c.2256+78_2256+79del NP_001304113.1:n.2256+78_2256+79del
NM_001317185.1:c.891+78_891+79del NP_001304114.1:n.891+78_891+79del
NM_001317186.1:c.474+78_474+79del NP_001304115.1:n.474+78_474+79del
NM_004360.4:c.2439+78_2439+79del NP_004351.1:n.2439+78_2439+79del
NM_004360.5:c.2439+78_2439+79del MANE Select NP_004351.1:n.2439+78_2439+79del
NM_001317184.2:c.2256+78_2256+79del NP_001304113.1:n.2256+78_2256+79del
NM_001317185.2:c.891+78_891+79del NP_001304114.1:n.891+78_891+79del
NM_001317186.2:c.474+78_474+79del NP_001304115.1:n.474+78_474+79del