Canonical Allele Identifier: CA2732913432
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs2152136579
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819162_68819185del , CM000678.2:g.68819162_68819185del GRCh38
NC_000016.9:g.68853065_68853088del , CM000678.1:g.68853065_68853088del GRCh37
NC_000016.8:g.67410566_67410589del NCBI36
NG_008021.1:g.86871_86894del , LRG_301:g.86871_86894del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1566-118_1566-95del MANE Select ENSP00000261769.4:n.1566-118_1566-95del
ENST00000261769.9:c.1566-118_1566-95del ENSP00000261769.4:n.1566-118_1566-95del
ENST00000422392.6:c.1383-118_1383-95del ENSP00000414946.2:n.1383-118_1383-95del
ENST00000562836.5:n.1637-118_1637-95del
ENST00000566510.5:c.*232-118_*232-95del ENSP00000458139.1:n.*232-118_*232-95del
ENST00000566612.5:c.1566-2839_1566-2816del ENSP00000454782.1:n.1566-2839_1566-2816del
ENST00000611625.4:c.1629-118_1629-95del ENSP00000481063.1:n.1629-118_1629-95del
ENST00000612417.4:c.1566-118_1566-95del ENSP00000478360.1:n.1566-118_1566-95del
ENST00000621016.4:c.1566-118_1566-95del ENSP00000480664.1:n.1566-118_1566-95del
NM_004360.3:c.1566-118_1566-95del , LRG_301t1:c.1566-118_1566-95del NP_004351.1:n.1566-118_1566-95del
XM_011523488.1:c.831-118_831-95del XP_011521790.1:n.831-118_831-95del
XM_011523489.1:c.831-118_831-95del XP_011521791.1:n.831-118_831-95del
NM_001317184.1:c.1383-118_1383-95del NP_001304113.1:n.1383-118_1383-95del
NM_001317185.1:c.18-118_18-95del NP_001304114.1:n.18-118_18-95del
NM_001317186.1:c.-254-2839_-254-2816del NP_001304115.1:n.-254-2839_-254-2816del
NM_004360.4:c.1566-118_1566-95del NP_004351.1:n.1566-118_1566-95del
NM_004360.5:c.1566-118_1566-95del MANE Select NP_004351.1:n.1566-118_1566-95del
NM_001317184.2:c.1383-118_1383-95del NP_001304113.1:n.1383-118_1383-95del
NM_001317185.2:c.18-118_18-95del NP_001304114.1:n.18-118_18-95del
NM_001317186.2:c.-254-2839_-254-2816del NP_001304115.1:n.-254-2839_-254-2816del
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