Canonical Allele Identifier: CA978527734
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829975_68829991del , CM000678.2:g.68829975_68829991del GRCh38
NC_000016.9:g.68863878_68863894del , CM000678.1:g.68863878_68863894del GRCh37
NC_000016.8:g.67421379_67421395del NCBI36
NG_008021.1:g.97684_97700del , LRG_301:g.97684_97700del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+178_2439+194del MANE Select ENSP00000261769.4:n.2439+178_2439+194del
ENST00000261769.9:c.2439+178_2439+194del ENSP00000261769.4:n.2439+178_2439+194del
ENST00000422392.6:c.2256+178_2256+194del ENSP00000414946.2:n.2256+178_2256+194del
ENST00000562118.1:n.657+178_657+194del
ENST00000562836.5:n.2510+178_2510+194del
ENST00000566510.5:c.*1105+178_*1105+194del ENSP00000458139.1:n.*1105+178_*1105+194del
ENST00000566612.5:c.*679+178_*679+194del ENSP00000454782.1:n.*679+178_*679+194del
ENST00000611625.4:c.2502+178_2502+194del ENSP00000481063.1:n.2502+178_2502+194del
ENST00000612417.4:c.1853+3421_1853+3437del ENSP00000478360.1:n.1853+3421_1853+3437del
ENST00000621016.4:c.1866-4228_1866-4212del ENSP00000480664.1:n.1866-4228_1866-4212del
NM_004360.3:c.2439+178_2439+194del , LRG_301t1:c.2439+178_2439+194del NP_004351.1:n.2439+178_2439+194del
XM_011523488.1:c.1704+178_1704+194del XP_011521790.1:n.1704+178_1704+194del
XM_011523489.1:c.1704+178_1704+194del XP_011521791.1:n.1704+178_1704+194del
NM_001317184.1:c.2256+178_2256+194del NP_001304113.1:n.2256+178_2256+194del
NM_001317185.1:c.891+178_891+194del NP_001304114.1:n.891+178_891+194del
NM_001317186.1:c.474+178_474+194del NP_001304115.1:n.474+178_474+194del
NM_004360.4:c.2439+178_2439+194del NP_004351.1:n.2439+178_2439+194del
NM_004360.5:c.2439+178_2439+194del MANE Select NP_004351.1:n.2439+178_2439+194del
NM_001317184.2:c.2256+178_2256+194del NP_001304113.1:n.2256+178_2256+194del
NM_001317185.2:c.891+178_891+194del NP_001304114.1:n.891+178_891+194del
NM_001317186.2:c.474+178_474+194del NP_001304115.1:n.474+178_474+194del