Canonical Allele Identifier: CA978527505
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1961437975
gnomAD v3: 16-68829906-CA-C
gnomAD v4: 16-68829906-CA-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829907del , CM000678.2:g.68829907del GRCh38
NC_000016.9:g.68863810del , CM000678.1:g.68863810del GRCh37
NC_000016.8:g.67421311del NCBI36
NG_008021.1:g.97616del , LRG_301:g.97616del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+110del MANE Select ENSP00000261769.4:n.2439+110del
ENST00000261769.9:c.2439+110del ENSP00000261769.4:n.2439+110del
ENST00000422392.6:c.2256+110del ENSP00000414946.2:n.2256+110del
ENST00000562118.1:n.657+110del
ENST00000562836.5:n.2510+110del
ENST00000566510.5:c.*1105+110del ENSP00000458139.1:n.*1105+110del
ENST00000566612.5:c.*679+110del ENSP00000454782.1:n.*679+110del
ENST00000611625.4:c.2502+110del ENSP00000481063.1:n.2502+110del
ENST00000612417.4:c.1853+3353del ENSP00000478360.1:n.1853+3353del
ENST00000621016.4:c.1866-4296del ENSP00000480664.1:n.1866-4296del
NM_004360.3:c.2439+110del , LRG_301t1:c.2439+110del NP_004351.1:n.2439+110del
XM_011523488.1:c.1704+110del XP_011521790.1:n.1704+110del
XM_011523489.1:c.1704+110del XP_011521791.1:n.1704+110del
NM_001317184.1:c.2256+110del NP_001304113.1:n.2256+110del
NM_001317185.1:c.891+110del NP_001304114.1:n.891+110del
NM_001317186.1:c.474+110del NP_001304115.1:n.474+110del
NM_004360.4:c.2439+110del NP_004351.1:n.2439+110del
NM_004360.5:c.2439+110del MANE Select NP_004351.1:n.2439+110del
NM_001317184.2:c.2256+110del NP_001304113.1:n.2256+110del
NM_001317185.2:c.891+110del NP_001304114.1:n.891+110del
NM_001317186.2:c.474+110del NP_001304115.1:n.474+110del
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