Canonical Allele Identifier: CA2633932035
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829895_68829896del , CM000678.2:g.68829895_68829896del GRCh38
NC_000016.9:g.68863798_68863799del , CM000678.1:g.68863798_68863799del GRCh37
NC_000016.8:g.67421299_67421300del NCBI36
NG_008021.1:g.97604_97605del , LRG_301:g.97604_97605del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+98_2439+99del MANE Select ENSP00000261769.4:n.2439+98_2439+99del
ENST00000261769.9:c.2439+98_2439+99del ENSP00000261769.4:n.2439+98_2439+99del
ENST00000422392.6:c.2256+98_2256+99del ENSP00000414946.2:n.2256+98_2256+99del
ENST00000562118.1:n.657+98_657+99del
ENST00000562836.5:n.2510+98_2510+99del
ENST00000566510.5:c.*1105+98_*1105+99del ENSP00000458139.1:n.*1105+98_*1105+99del
ENST00000566612.5:c.*679+98_*679+99del ENSP00000454782.1:n.*679+98_*679+99del
ENST00000611625.4:c.2502+98_2502+99del ENSP00000481063.1:n.2502+98_2502+99del
ENST00000612417.4:c.1853+3341_1853+3342del ENSP00000478360.1:n.1853+3341_1853+3342del
ENST00000621016.4:c.1866-4308_1866-4307del ENSP00000480664.1:n.1866-4308_1866-4307del
NM_004360.3:c.2439+98_2439+99del , LRG_301t1:c.2439+98_2439+99del NP_004351.1:n.2439+98_2439+99del
XM_011523488.1:c.1704+98_1704+99del XP_011521790.1:n.1704+98_1704+99del
XM_011523489.1:c.1704+98_1704+99del XP_011521791.1:n.1704+98_1704+99del
NM_001317184.1:c.2256+98_2256+99del NP_001304113.1:n.2256+98_2256+99del
NM_001317185.1:c.891+98_891+99del NP_001304114.1:n.891+98_891+99del
NM_001317186.1:c.474+98_474+99del NP_001304115.1:n.474+98_474+99del
NM_004360.4:c.2439+98_2439+99del NP_004351.1:n.2439+98_2439+99del
NM_004360.5:c.2439+98_2439+99del MANE Select NP_004351.1:n.2439+98_2439+99del
NM_001317184.2:c.2256+98_2256+99del NP_001304113.1:n.2256+98_2256+99del
NM_001317185.2:c.891+98_891+99del NP_001304114.1:n.891+98_891+99del
NM_001317186.2:c.474+98_474+99del NP_001304115.1:n.474+98_474+99del