Canonical Allele Identifier: CA2695223618
Gene: CDH1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819280_68819288del , CM000678.2:g.68819280_68819288del GRCh38
NC_000016.9:g.68853183_68853191del , CM000678.1:g.68853183_68853191del GRCh37
NC_000016.8:g.67410684_67410692del NCBI36
NG_008021.1:g.86989_86997del , LRG_301:g.86989_86997del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1566_1574del MANE Select ENSP00000261769.4:p.Tyr523_Ile525del
ENST00000261769.9:c.1566_1574del ENSP00000261769.4:p.Tyr523_Ile525del
ENST00000422392.6:c.1383_1391del ENSP00000414946.2:p.Tyr462_Ile464del
ENST00000562836.5:n.1637_1645del
ENST00000566510.5:c.*232_*240del ENSP00000458139.1:n.*232_*240del
ENST00000566612.5:c.1566-2721_1566-2713del ENSP00000454782.1:n.1566-2721_1566-2713del
ENST00000611625.4:c.1629_1637del ENSP00000481063.1:p.Tyr544_Ile546del
ENST00000612417.4:c.1566_1574del ENSP00000478360.1:p.Tyr523_Ile525del
ENST00000621016.4:c.1566_1574del ENSP00000480664.1:p.Tyr523_Ile525del
NM_004360.3:c.1566_1574del , LRG_301t1:c.1566_1574del NP_004351.1:p.Tyr523_Ile525del
XM_011523488.1:c.831_839del XP_011521790.1:p.Tyr278_Ile280del
XM_011523489.1:c.831_839del XP_011521791.1:p.Tyr278_Ile280del
NM_001317184.1:c.1383_1391del NP_001304113.1:p.Tyr462_Ile464del
NM_001317185.1:c.18_26del NP_001304114.1:p.Tyr7_Ile9del
NM_001317186.1:c.-254-2721_-254-2713del NP_001304115.1:n.-254-2721_-254-2713del
NM_004360.4:c.1566_1574del NP_004351.1:p.Tyr523_Ile525del
NM_004360.5:c.1566_1574del MANE Select NP_004351.1:p.Tyr523_Ile525del
NM_001317184.2:c.1383_1391del NP_001304113.1:p.Tyr462_Ile464del
NM_001317185.2:c.18_26del NP_001304114.1:p.Tyr7_Ile9del
NM_001317186.2:c.-254-2721_-254-2713del NP_001304115.1:n.-254-2721_-254-2713del
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