Canonical Allele Identifier: CA2633931728
Gene: CDH1 HGNC NCBI

Linked Data

gnomAD v4: 16-68819200-CTG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819201_68819202del , CM000678.2:g.68819201_68819202del GRCh38
NC_000016.9:g.68853104_68853105del , CM000678.1:g.68853104_68853105del GRCh37
NC_000016.8:g.67410605_67410606del NCBI36
NG_008021.1:g.86910_86911del , LRG_301:g.86910_86911del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1566-79_1566-78del MANE Select ENSP00000261769.4:n.1566-79_1566-78del
ENST00000261769.9:c.1566-79_1566-78del ENSP00000261769.4:n.1566-79_1566-78del
ENST00000422392.6:c.1383-79_1383-78del ENSP00000414946.2:n.1383-79_1383-78del
ENST00000562836.5:n.1637-79_1637-78del
ENST00000566510.5:c.*232-79_*232-78del ENSP00000458139.1:n.*232-79_*232-78del
ENST00000566612.5:c.1566-2800_1566-2799del ENSP00000454782.1:n.1566-2800_1566-2799del
ENST00000611625.4:c.1629-79_1629-78del ENSP00000481063.1:n.1629-79_1629-78del
ENST00000612417.4:c.1566-79_1566-78del ENSP00000478360.1:n.1566-79_1566-78del
ENST00000621016.4:c.1566-79_1566-78del ENSP00000480664.1:n.1566-79_1566-78del
NM_004360.3:c.1566-79_1566-78del , LRG_301t1:c.1566-79_1566-78del NP_004351.1:n.1566-79_1566-78del
XM_011523488.1:c.831-79_831-78del XP_011521790.1:n.831-79_831-78del
XM_011523489.1:c.831-79_831-78del XP_011521791.1:n.831-79_831-78del
NM_001317184.1:c.1383-79_1383-78del NP_001304113.1:n.1383-79_1383-78del
NM_001317185.1:c.18-79_18-78del NP_001304114.1:n.18-79_18-78del
NM_001317186.1:c.-254-2800_-254-2799del NP_001304115.1:n.-254-2800_-254-2799del
NM_004360.4:c.1566-79_1566-78del NP_004351.1:n.1566-79_1566-78del
NM_004360.5:c.1566-79_1566-78del MANE Select NP_004351.1:n.1566-79_1566-78del
NM_001317184.2:c.1383-79_1383-78del NP_001304113.1:n.1383-79_1383-78del
NM_001317185.2:c.18-79_18-78del NP_001304114.1:n.18-79_18-78del
NM_001317186.2:c.-254-2800_-254-2799del NP_001304115.1:n.-254-2800_-254-2799del
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