Canonical Allele Identifier: CA283318438
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs993310507

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829959_68829968del , CM000678.2:g.68829959_68829968del GRCh38
NC_000016.9:g.68863862_68863871del , CM000678.1:g.68863862_68863871del GRCh37
NC_000016.8:g.67421363_67421372del NCBI36
NG_008021.1:g.97668_97677del , LRG_301:g.97668_97677del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+162_2439+171del MANE Select ENSP00000261769.4:n.2439+162_2439+171del
ENST00000261769.9:c.2439+162_2439+171del ENSP00000261769.4:n.2439+162_2439+171del
ENST00000422392.6:c.2256+162_2256+171del ENSP00000414946.2:n.2256+162_2256+171del
ENST00000562118.1:n.657+162_657+171del
ENST00000562836.5:n.2510+162_2510+171del
ENST00000566510.5:c.*1105+162_*1105+171del ENSP00000458139.1:n.*1105+162_*1105+171del
ENST00000566612.5:c.*679+162_*679+171del ENSP00000454782.1:n.*679+162_*679+171del
ENST00000611625.4:c.2502+162_2502+171del ENSP00000481063.1:n.2502+162_2502+171del
ENST00000612417.4:c.1853+3405_1853+3414del ENSP00000478360.1:n.1853+3405_1853+3414del
ENST00000621016.4:c.1866-4244_1866-4235del ENSP00000480664.1:n.1866-4244_1866-4235del
NM_004360.3:c.2439+162_2439+171del , LRG_301t1:c.2439+162_2439+171del NP_004351.1:n.2439+162_2439+171del
XM_011523488.1:c.1704+162_1704+171del XP_011521790.1:n.1704+162_1704+171del
XM_011523489.1:c.1704+162_1704+171del XP_011521791.1:n.1704+162_1704+171del
NM_001317184.1:c.2256+162_2256+171del NP_001304113.1:n.2256+162_2256+171del
NM_001317185.1:c.891+162_891+171del NP_001304114.1:n.891+162_891+171del
NM_001317186.1:c.474+162_474+171del NP_001304115.1:n.474+162_474+171del
NM_004360.4:c.2439+162_2439+171del NP_004351.1:n.2439+162_2439+171del
NM_004360.5:c.2439+162_2439+171del MANE Select NP_004351.1:n.2439+162_2439+171del
NM_001317184.2:c.2256+162_2256+171del NP_001304113.1:n.2256+162_2256+171del
NM_001317185.2:c.891+162_891+171del NP_001304114.1:n.891+162_891+171del
NM_001317186.2:c.474+162_474+171del NP_001304115.1:n.474+162_474+171del