Canonical Allele Identifier: CA891837769
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965389_87965391delinsCAA , CM000672.2:g.87965389_87965391delinsCAA GRCh38
NC_000010.10:g.89725146_89725148delinsCAA , CM000672.1:g.89725146_89725148delinsCAA GRCh37
NC_000010.9:g.89715126_89715128delinsCAA NCBI36
NG_007466.2:g.106951_106953delinsCAA , LRG_311:g.106951_106953delinsCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1222_1224delinsCAA ENSP00000514759.2:p.Tyr408Gln
ENST00000710265.1:c.*158_*160delinsCAA ENSP00000518161.1:n.*158_*160delinsCAA
ENST00000688158.2:n.1864_1866delinsCAA
ENST00000688922.2:c.*959_*961delinsCAA ENSP00000508742.2:n.*959_*961delinsCAA
ENST00000700021.1:c.1084_1086delinsCAA ENSP00000514757.1:p.Tyr362Gln
ENST00000700022.1:c.*468_*470delinsCAA ENSP00000514758.1:n.*468_*470delinsCAA
ENST00000700023.1:n.2287_2289delinsCAA
ENST00000700024.1:n.2521_2523delinsCAA
ENST00000706954.1:c.1129_1131delinsCAA ENSP00000516674.1:p.Tyr377Gln
ENST00000706955.1:c.*1164_*1166delinsCAA ENSP00000516675.1:n.*1164_*1166delinsCAA
ENST00000686459.1:c.*715_*717delinsCAA ENSP00000508909.1:n.*715_*717delinsCAA
ENST00000688158.1:c.*1240_*1242delinsCAA ENSP00000509254.1:n.*1240_*1242delinsCAA
ENST00000688308.1:c.1129_1131delinsCAA ENSP00000508752.1:p.Tyr377Gln
ENST00000688922.1:c.1050_1052delinsCAA
ENST00000693560.1:c.1648_1650delinsCAA ENSP00000509861.1:p.Tyr550Gln
ENST00000371953.8:c.1129_1131delinsCAA MANE Select ENSP00000361021.3:p.Tyr377Gln
ENST00000371953.7:c.1129_1131delinsCAA ENSP00000361021.3:p.Tyr377Gln
NM_000314.5:c.1129_1131delinsCAA NP_000305.3:p.Tyr377Gln
NM_000314.6:c.1129_1131delinsCAA NP_000305.3:p.Tyr377Gln
NM_001304717.2:c.1648_1650delinsCAA NP_001291646.2:p.Tyr550Gln
NM_001304718.1:c.538_540delinsCAA NP_001291647.1:p.Tyr180Gln
XM_006717926.2:c.1084_1086delinsCAA XP_006717989.1:p.Tyr362Gln
XM_011539982.1:c.1033_1035delinsCAA XP_011538284.1:p.Tyr345Gln
XR_945791.1:n.1699_1701delinsCAA
NM_000314.7:c.1129_1131delinsCAA NP_000305.3:p.Tyr377Gln
NM_001304717.5:c.1648_1650delinsCAA NP_001291646.4:p.Tyr550Gln
NM_001304718.2:c.538_540delinsCAA NP_001291647.1:p.Tyr180Gln
NM_000314.8:c.1129_1131delinsCAA MANE Select NP_000305.3:p.Tyr377Gln