Canonical Allele Identifier: CA891837965
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965416_87965418delinsTAA , CM000672.2:g.87965416_87965418delinsTAA GRCh38
NC_000010.10:g.89725173_89725175delinsTAA , CM000672.1:g.89725173_89725175delinsTAA GRCh37
NC_000010.9:g.89715153_89715155delinsTAA NCBI36
NG_007466.2:g.106978_106980delinsTAA , LRG_311:g.106978_106980delinsTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1249_1251delinsTAA ENSP00000514759.2:p.Asp417Ter
ENST00000710265.1:c.*185_*187delinsTAA ENSP00000518161.1:n.*185_*187delinsTAA
ENST00000688158.2:n.1891_1893delinsTAA
ENST00000688922.2:c.*986_*988delinsTAA ENSP00000508742.2:n.*986_*988delinsTAA
ENST00000700021.1:c.1111_1113delinsTAA ENSP00000514757.1:p.Asp371Ter
ENST00000700022.1:c.*495_*497delinsTAA ENSP00000514758.1:n.*495_*497delinsTAA
ENST00000700023.1:n.2314_2316delinsTAA
ENST00000700024.1:n.2548_2550delinsTAA
ENST00000706954.1:c.1156_1158delinsTAA ENSP00000516674.1:p.Asp386Ter
ENST00000706955.1:c.*1191_*1193delinsTAA ENSP00000516675.1:n.*1191_*1193delinsTAA
ENST00000686459.1:c.*742_*744delinsTAA ENSP00000508909.1:n.*742_*744delinsTAA
ENST00000688158.1:c.*1267_*1269delinsTAA ENSP00000509254.1:n.*1267_*1269delinsTAA
ENST00000688308.1:c.1156_1158delinsTAA ENSP00000508752.1:p.Asp386Ter
ENST00000688922.1:c.1077_1079delinsTAA
ENST00000693560.1:c.1675_1677delinsTAA ENSP00000509861.1:p.Asp559Ter
ENST00000371953.8:c.1156_1158delinsTAA MANE Select ENSP00000361021.3:p.Asp386Ter
ENST00000371953.7:c.1156_1158delinsTAA ENSP00000361021.3:p.Asp386Ter
NM_000314.5:c.1156_1158delinsTAA NP_000305.3:p.Asp386Ter
NM_000314.6:c.1156_1158delinsTAA NP_000305.3:p.Asp386Ter
NM_001304717.2:c.1675_1677delinsTAA NP_001291646.2:p.Asp559Ter
NM_001304718.1:c.565_567delinsTAA NP_001291647.1:p.Asp189Ter
XM_006717926.2:c.1111_1113delinsTAA XP_006717989.1:p.Asp371Ter
XM_011539982.1:c.1060_1062delinsTAA XP_011538284.1:p.Asp354Ter
XR_945791.1:n.1726_1728delinsTAA
NM_000314.7:c.1156_1158delinsTAA NP_000305.3:p.Asp386Ter
NM_001304717.5:c.1675_1677delinsTAA NP_001291646.4:p.Asp559Ter
NM_001304718.2:c.565_567delinsTAA NP_001291647.1:p.Asp189Ter
NM_000314.8:c.1156_1158delinsTAA MANE Select NP_000305.3:p.Asp386Ter