Canonical Allele Identifier: CA891837170
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965321_87965322delinsAA , CM000672.2:g.87965321_87965322delinsAA GRCh38
NC_000010.10:g.89725078_89725079delinsAA , CM000672.1:g.89725078_89725079delinsAA GRCh37
NC_000010.9:g.89715058_89715059delinsAA NCBI36
NG_007466.2:g.106883_106884delinsAA , LRG_311:g.106883_106884delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1154_1155delinsAA ENSP00000514759.2:p.Pro385Gln
ENST00000710265.1:c.*90_*91delinsAA ENSP00000518161.1:n.*90_*91delinsAA
ENST00000688158.2:n.1796_1797delinsAA
ENST00000688922.2:c.*891_*892delinsAA ENSP00000508742.2:n.*891_*892delinsAA
ENST00000700021.1:c.1016_1017delinsAA ENSP00000514757.1:p.Pro339Gln
ENST00000700022.1:c.*400_*401delinsAA ENSP00000514758.1:n.*400_*401delinsAA
ENST00000700023.1:n.2219_2220delinsAA
ENST00000700024.1:n.2453_2454delinsAA
ENST00000706954.1:c.1061_1062delinsAA ENSP00000516674.1:p.Pro354Gln
ENST00000706955.1:c.*1096_*1097delinsAA ENSP00000516675.1:n.*1096_*1097delinsAA
ENST00000686459.1:c.*647_*648delinsAA ENSP00000508909.1:n.*647_*648delinsAA
ENST00000688158.1:c.*1172_*1173delinsAA ENSP00000509254.1:n.*1172_*1173delinsAA
ENST00000688308.1:c.1061_1062delinsAA ENSP00000508752.1:p.Pro354Gln
ENST00000688922.1:c.982_983delinsAA
ENST00000693560.1:c.1580_1581delinsAA ENSP00000509861.1:p.Pro527Gln
ENST00000371953.8:c.1061_1062delinsAA MANE Select ENSP00000361021.3:p.Pro354Gln
ENST00000371953.7:c.1061_1062delinsAA ENSP00000361021.3:p.Pro354Gln
NM_000314.5:c.1061_1062delinsAA NP_000305.3:p.Pro354Gln
NM_000314.6:c.1061_1062delinsAA NP_000305.3:p.Pro354Gln
NM_001304717.2:c.1580_1581delinsAA NP_001291646.2:p.Pro527Gln
NM_001304718.1:c.470_471delinsAA NP_001291647.1:p.Pro157Gln
XM_006717926.2:c.1016_1017delinsAA XP_006717989.1:p.Pro339Gln
XM_011539982.1:c.965_966delinsAA XP_011538284.1:p.Pro322Gln
XR_945791.1:n.1631_1632delinsAA
NM_000314.7:c.1061_1062delinsAA NP_000305.3:p.Pro354Gln
NM_001304717.5:c.1580_1581delinsAA NP_001291646.4:p.Pro527Gln
NM_001304718.2:c.470_471delinsAA NP_001291647.1:p.Pro157Gln
NM_000314.8:c.1061_1062delinsAA MANE Select NP_000305.3:p.Pro354Gln