Canonical Allele Identifier: CA891841587
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965347_87965348delinsCG , CM000672.2:g.87965347_87965348delinsCG GRCh38
NC_000010.10:g.89725104_89725105delinsCG , CM000672.1:g.89725104_89725105delinsCG GRCh37
NC_000010.9:g.89715084_89715085delinsCG NCBI36
NG_007466.2:g.106909_106910delinsCG , LRG_311:g.106909_106910delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1180_1181delinsCG ENSP00000514759.2:p.Thr394Arg
ENST00000710265.1:c.*116_*117delinsCG ENSP00000518161.1:n.*116_*117delinsCG
ENST00000688158.2:n.1822_1823delinsCG
ENST00000688922.2:c.*917_*918delinsCG ENSP00000508742.2:n.*917_*918delinsCG
ENST00000700021.1:c.1042_1043delinsCG ENSP00000514757.1:p.Thr348Arg
ENST00000700022.1:c.*426_*427delinsCG ENSP00000514758.1:n.*426_*427delinsCG
ENST00000700023.1:n.2245_2246delinsCG
ENST00000700024.1:n.2479_2480delinsCG
ENST00000706954.1:c.1087_1088delinsCG ENSP00000516674.1:p.Thr363Arg
ENST00000706955.1:c.*1122_*1123delinsCG ENSP00000516675.1:n.*1122_*1123delinsCG
ENST00000686459.1:c.*673_*674delinsCG ENSP00000508909.1:n.*673_*674delinsCG
ENST00000688158.1:c.*1198_*1199delinsCG ENSP00000509254.1:n.*1198_*1199delinsCG
ENST00000688308.1:c.1087_1088delinsCG ENSP00000508752.1:p.Thr363Arg
ENST00000688922.1:c.1008_1009delinsCG
ENST00000693560.1:c.1606_1607delinsCG ENSP00000509861.1:p.Thr536Arg
ENST00000371953.8:c.1087_1088delinsCG MANE Select ENSP00000361021.3:p.Thr363Arg
ENST00000371953.7:c.1087_1088delinsCG ENSP00000361021.3:p.Thr363Arg
NM_000314.5:c.1087_1088delinsCG NP_000305.3:p.Thr363Arg
NM_000314.6:c.1087_1088delinsCG NP_000305.3:p.Thr363Arg
NM_001304717.2:c.1606_1607delinsCG NP_001291646.2:p.Thr536Arg
NM_001304718.1:c.496_497delinsCG NP_001291647.1:p.Thr166Arg
XM_006717926.2:c.1042_1043delinsCG XP_006717989.1:p.Thr348Arg
XM_011539982.1:c.991_992delinsCG XP_011538284.1:p.Thr331Arg
XR_945791.1:n.1657_1658delinsCG
NM_000314.7:c.1087_1088delinsCG NP_000305.3:p.Thr363Arg
NM_001304717.5:c.1606_1607delinsCG NP_001291646.4:p.Thr536Arg
NM_001304718.2:c.496_497delinsCG NP_001291647.1:p.Thr166Arg
NM_000314.8:c.1087_1088delinsCG MANE Select NP_000305.3:p.Thr363Arg