Canonical Allele Identifier: CA2633932057
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829924_68829931del , CM000678.2:g.68829924_68829931del GRCh38
NC_000016.9:g.68863827_68863834del , CM000678.1:g.68863827_68863834del GRCh37
NC_000016.8:g.67421328_67421335del NCBI36
NG_008021.1:g.97633_97640del , LRG_301:g.97633_97640del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+127_2439+134del MANE Select ENSP00000261769.4:n.2439+127_2439+134del
ENST00000261769.9:c.2439+127_2439+134del ENSP00000261769.4:n.2439+127_2439+134del
ENST00000422392.6:c.2256+127_2256+134del ENSP00000414946.2:n.2256+127_2256+134del
ENST00000562118.1:n.657+127_657+134del
ENST00000562836.5:n.2510+127_2510+134del
ENST00000566510.5:c.*1105+127_*1105+134del ENSP00000458139.1:n.*1105+127_*1105+134del
ENST00000566612.5:c.*679+127_*679+134del ENSP00000454782.1:n.*679+127_*679+134del
ENST00000611625.4:c.2502+127_2502+134del ENSP00000481063.1:n.2502+127_2502+134del
ENST00000612417.4:c.1853+3370_1853+3377del ENSP00000478360.1:n.1853+3370_1853+3377del
ENST00000621016.4:c.1866-4279_1866-4272del ENSP00000480664.1:n.1866-4279_1866-4272del
NM_004360.3:c.2439+127_2439+134del , LRG_301t1:c.2439+127_2439+134del NP_004351.1:n.2439+127_2439+134del
XM_011523488.1:c.1704+127_1704+134del XP_011521790.1:n.1704+127_1704+134del
XM_011523489.1:c.1704+127_1704+134del XP_011521791.1:n.1704+127_1704+134del
NM_001317184.1:c.2256+127_2256+134del NP_001304113.1:n.2256+127_2256+134del
NM_001317185.1:c.891+127_891+134del NP_001304114.1:n.891+127_891+134del
NM_001317186.1:c.474+127_474+134del NP_001304115.1:n.474+127_474+134del
NM_004360.4:c.2439+127_2439+134del NP_004351.1:n.2439+127_2439+134del
NM_004360.5:c.2439+127_2439+134del MANE Select NP_004351.1:n.2439+127_2439+134del
NM_001317184.2:c.2256+127_2256+134del NP_001304113.1:n.2256+127_2256+134del
NM_001317185.2:c.891+127_891+134del NP_001304114.1:n.891+127_891+134del
NM_001317186.2:c.474+127_474+134del NP_001304115.1:n.474+127_474+134del