Canonical Allele Identifier: CA891837926
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965408_87965409delinsTG , CM000672.2:g.87965408_87965409delinsTG GRCh38
NC_000010.10:g.89725165_89725166delinsTG , CM000672.1:g.89725165_89725166delinsTG GRCh37
NC_000010.9:g.89715145_89715146delinsTG NCBI36
NG_007466.2:g.106970_106971delinsTG , LRG_311:g.106970_106971delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1241_1242delinsTG ENSP00000514759.2:p.Thr414Met
ENST00000710265.1:c.*177_*178delinsTG ENSP00000518161.1:n.*177_*178delinsTG
ENST00000688158.2:n.1883_1884delinsTG
ENST00000688922.2:c.*978_*979delinsTG ENSP00000508742.2:n.*978_*979delinsTG
ENST00000700021.1:c.1103_1104delinsTG ENSP00000514757.1:p.Thr368Met
ENST00000700022.1:c.*487_*488delinsTG ENSP00000514758.1:n.*487_*488delinsTG
ENST00000700023.1:n.2306_2307delinsTG
ENST00000700024.1:n.2540_2541delinsTG
ENST00000706954.1:c.1148_1149delinsTG ENSP00000516674.1:p.Thr383Met
ENST00000706955.1:c.*1183_*1184delinsTG ENSP00000516675.1:n.*1183_*1184delinsTG
ENST00000686459.1:c.*734_*735delinsTG ENSP00000508909.1:n.*734_*735delinsTG
ENST00000688158.1:c.*1259_*1260delinsTG ENSP00000509254.1:n.*1259_*1260delinsTG
ENST00000688308.1:c.1148_1149delinsTG ENSP00000508752.1:p.Thr383Met
ENST00000688922.1:c.1069_1070delinsTG
ENST00000693560.1:c.1667_1668delinsTG ENSP00000509861.1:p.Thr556Met
ENST00000371953.8:c.1148_1149delinsTG MANE Select ENSP00000361021.3:p.Thr383Met
ENST00000371953.7:c.1148_1149delinsTG ENSP00000361021.3:p.Thr383Met
NM_000314.5:c.1148_1149delinsTG NP_000305.3:p.Thr383Met
NM_000314.6:c.1148_1149delinsTG NP_000305.3:p.Thr383Met
NM_001304717.2:c.1667_1668delinsTG NP_001291646.2:p.Thr556Met
NM_001304718.1:c.557_558delinsTG NP_001291647.1:p.Thr186Met
XM_006717926.2:c.1103_1104delinsTG XP_006717989.1:p.Thr368Met
XM_011539982.1:c.1052_1053delinsTG XP_011538284.1:p.Thr351Met
XR_945791.1:n.1718_1719delinsTG
NM_000314.7:c.1148_1149delinsTG NP_000305.3:p.Thr383Met
NM_001304717.5:c.1667_1668delinsTG NP_001291646.4:p.Thr556Met
NM_001304718.2:c.557_558delinsTG NP_001291647.1:p.Thr186Met
NM_000314.8:c.1148_1149delinsTG MANE Select NP_000305.3:p.Thr383Met