Canonical Allele Identifier: CA645553901
Gene: PTEN HGNC NCBI

Linked Data

COSMIC: COSM249829

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87952187_87952189del , CM000672.2:g.87952187_87952189del GRCh38
NC_000010.10:g.89711944_89711946del , CM000672.1:g.89711944_89711946del GRCh37
NC_000010.9:g.89701924_89701926del NCBI36
NG_007466.2:g.93749_93751del , LRG_311:g.93749_93751del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.562_564del ENSP00000514759.2:p.Tyr188del
ENST00000710265.1:c.562_564del ENSP00000518161.1:p.Tyr188del
ENST00000472832.3:c.562_564del ENSP00000483066.2:p.Tyr188del
ENST00000688158.2:n.1297_1299del
ENST00000688922.2:c.*392_*394del ENSP00000508742.2:n.*392_*394del
ENST00000700021.1:c.517_519del ENSP00000514757.1:p.Tyr173del
ENST00000700022.1:c.493-5666_493-5664del ENSP00000514758.1:n.493-5666_493-5664del
ENST00000700023.1:n.1720_1722del
ENST00000700024.1:n.1954_1956del
ENST00000700025.1:n.1331_1333del
ENST00000700029.1:c.396_398del
ENST00000706954.1:c.562_564del ENSP00000516674.1:p.Tyr188del
ENST00000706955.1:c.*597_*599del ENSP00000516675.1:n.*597_*599del
ENST00000686459.1:c.*148_*150del ENSP00000508909.1:n.*148_*150del
ENST00000688158.1:c.*673_*675del ENSP00000509254.1:n.*673_*675del
ENST00000688308.1:c.562_564del ENSP00000508752.1:p.Tyr188del
ENST00000688922.1:c.483_485del
ENST00000693560.1:c.1081_1083del ENSP00000509861.1:p.Tyr361del
ENST00000371953.8:c.562_564del MANE Select ENSP00000361021.3:p.Tyr188del
ENST00000371953.7:c.562_564del ENSP00000361021.3:p.Tyr188del
NM_000314.5:c.562_564del NP_000305.3:p.Tyr188del
NM_000314.6:c.562_564del NP_000305.3:p.Tyr188del
NM_001304717.2:c.1081_1083del NP_001291646.2:p.Tyr361del
NM_001304718.1:c.-30_-28del NP_001291647.1:n.-30_-28del
XM_006717926.2:c.517_519del XP_006717989.1:p.Tyr173del
XM_011539981.1:c.562_564del XP_011538283.1:p.Tyr188del
XM_011539982.1:c.466_468del XP_011538284.1:p.Tyr156del
XR_945791.1:n.1205-5666_1205-5664del
NM_000314.7:c.562_564del NP_000305.3:p.Tyr188del
NM_001304717.5:c.1081_1083del NP_001291646.4:p.Tyr361del
NM_001304718.2:c.-30_-28del NP_001291647.1:n.-30_-28del
NM_000314.8:c.562_564del MANE Select NP_000305.3:p.Tyr188del