Canonical Allele Identifier: CA2633931748
Gene: CDH1 HGNC NCBI

Linked Data

gnomAD v4: 16-68819231-ATGT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819236_68819238del , CM000678.2:g.68819236_68819238del GRCh38
NC_000016.9:g.68853139_68853141del , CM000678.1:g.68853139_68853141del GRCh37
NC_000016.8:g.67410640_67410642del NCBI36
NG_008021.1:g.86945_86947del , LRG_301:g.86945_86947del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1566-44_1566-42del MANE Select ENSP00000261769.4:n.1566-44_1566-42del
ENST00000261769.9:c.1566-44_1566-42del ENSP00000261769.4:n.1566-44_1566-42del
ENST00000422392.6:c.1383-44_1383-42del ENSP00000414946.2:n.1383-44_1383-42del
ENST00000562836.5:n.1637-44_1637-42del
ENST00000566510.5:c.*232-44_*232-42del ENSP00000458139.1:n.*232-44_*232-42del
ENST00000566612.5:c.1566-2765_1566-2763del ENSP00000454782.1:n.1566-2765_1566-2763del
ENST00000611625.4:c.1629-44_1629-42del ENSP00000481063.1:n.1629-44_1629-42del
ENST00000612417.4:c.1566-44_1566-42del ENSP00000478360.1:n.1566-44_1566-42del
ENST00000621016.4:c.1566-44_1566-42del ENSP00000480664.1:n.1566-44_1566-42del
NM_004360.3:c.1566-44_1566-42del , LRG_301t1:c.1566-44_1566-42del NP_004351.1:n.1566-44_1566-42del
XM_011523488.1:c.831-44_831-42del XP_011521790.1:n.831-44_831-42del
XM_011523489.1:c.831-44_831-42del XP_011521791.1:n.831-44_831-42del
NM_001317184.1:c.1383-44_1383-42del NP_001304113.1:n.1383-44_1383-42del
NM_001317185.1:c.18-44_18-42del NP_001304114.1:n.18-44_18-42del
NM_001317186.1:c.-254-2765_-254-2763del NP_001304115.1:n.-254-2765_-254-2763del
NM_004360.4:c.1566-44_1566-42del NP_004351.1:n.1566-44_1566-42del
NM_004360.5:c.1566-44_1566-42del MANE Select NP_004351.1:n.1566-44_1566-42del
NM_001317184.2:c.1383-44_1383-42del NP_001304113.1:n.1383-44_1383-42del
NM_001317185.2:c.18-44_18-42del NP_001304114.1:n.18-44_18-42del
NM_001317186.2:c.-254-2765_-254-2763del NP_001304115.1:n.-254-2765_-254-2763del
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