Canonical Allele Identifier: CA2579926462
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965408_87965409delinsGA , CM000672.2:g.87965408_87965409delinsGA GRCh38
NC_000010.10:g.89725165_89725166delinsGA , CM000672.1:g.89725165_89725166delinsGA GRCh37
NC_000010.9:g.89715145_89715146delinsGA NCBI36
NG_007466.2:g.106970_106971delinsGA , LRG_311:g.106970_106971delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1241_1242delinsGA ENSP00000514759.2:p.Thr414Arg
ENST00000710265.1:c.*177_*178delinsGA ENSP00000518161.1:n.*177_*178delinsGA
ENST00000688158.2:n.1883_1884delinsGA
ENST00000688922.2:c.*978_*979delinsGA ENSP00000508742.2:n.*978_*979delinsGA
ENST00000700021.1:c.1103_1104delinsGA ENSP00000514757.1:p.Thr368Arg
ENST00000700022.1:c.*487_*488delinsGA ENSP00000514758.1:n.*487_*488delinsGA
ENST00000700023.1:n.2306_2307delinsGA
ENST00000700024.1:n.2540_2541delinsGA
ENST00000706954.1:c.1148_1149delinsGA ENSP00000516674.1:p.Thr383Arg
ENST00000706955.1:c.*1183_*1184delinsGA ENSP00000516675.1:n.*1183_*1184delinsGA
ENST00000686459.1:c.*734_*735delinsGA ENSP00000508909.1:n.*734_*735delinsGA
ENST00000688158.1:c.*1259_*1260delinsGA ENSP00000509254.1:n.*1259_*1260delinsGA
ENST00000688308.1:c.1148_1149delinsGA ENSP00000508752.1:p.Thr383Arg
ENST00000688922.1:c.1069_1070delinsGA
ENST00000693560.1:c.1667_1668delinsGA ENSP00000509861.1:p.Thr556Arg
ENST00000371953.8:c.1148_1149delinsGA MANE Select ENSP00000361021.3:p.Thr383Arg
ENST00000371953.7:c.1148_1149delinsGA ENSP00000361021.3:p.Thr383Arg
NM_000314.5:c.1148_1149delinsGA NP_000305.3:p.Thr383Arg
NM_000314.6:c.1148_1149delinsGA NP_000305.3:p.Thr383Arg
NM_001304717.2:c.1667_1668delinsGA NP_001291646.2:p.Thr556Arg
NM_001304718.1:c.557_558delinsGA NP_001291647.1:p.Thr186Arg
XM_006717926.2:c.1103_1104delinsGA XP_006717989.1:p.Thr368Arg
XM_011539982.1:c.1052_1053delinsGA XP_011538284.1:p.Thr351Arg
XR_945791.1:n.1718_1719delinsGA
NM_000314.7:c.1148_1149delinsGA NP_000305.3:p.Thr383Arg
NM_001304717.5:c.1667_1668delinsGA NP_001291646.4:p.Thr556Arg
NM_001304718.2:c.557_558delinsGA NP_001291647.1:p.Thr186Arg
NM_000314.8:c.1148_1149delinsGA MANE Select NP_000305.3:p.Thr383Arg