Canonical Allele Identifier: CA891837092
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965315_87965316delinsTT , CM000672.2:g.87965315_87965316delinsTT GRCh38
NC_000010.10:g.89725072_89725073delinsTT , CM000672.1:g.89725072_89725073delinsTT GRCh37
NC_000010.9:g.89715052_89715053delinsTT NCBI36
NG_007466.2:g.106877_106878delinsTT , LRG_311:g.106877_106878delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1148_1149delinsTT ENSP00000514759.2:p.Glu383Val
ENST00000710265.1:c.*84_*85delinsTT ENSP00000518161.1:n.*84_*85delinsTT
ENST00000688158.2:n.1790_1791delinsTT
ENST00000688922.2:c.*885_*886delinsTT ENSP00000508742.2:n.*885_*886delinsTT
ENST00000700021.1:c.1010_1011delinsTT ENSP00000514757.1:p.Glu337Val
ENST00000700022.1:c.*394_*395delinsTT ENSP00000514758.1:n.*394_*395delinsTT
ENST00000700023.1:n.2213_2214delinsTT
ENST00000700024.1:n.2447_2448delinsTT
ENST00000706954.1:c.1055_1056delinsTT ENSP00000516674.1:p.Glu352Val
ENST00000706955.1:c.*1090_*1091delinsTT ENSP00000516675.1:n.*1090_*1091delinsTT
ENST00000686459.1:c.*641_*642delinsTT ENSP00000508909.1:n.*641_*642delinsTT
ENST00000688158.1:c.*1166_*1167delinsTT ENSP00000509254.1:n.*1166_*1167delinsTT
ENST00000688308.1:c.1055_1056delinsTT ENSP00000508752.1:p.Glu352Val
ENST00000688922.1:c.976_977delinsTT
ENST00000693560.1:c.1574_1575delinsTT ENSP00000509861.1:p.Glu525Val
ENST00000371953.8:c.1055_1056delinsTT MANE Select ENSP00000361021.3:p.Glu352Val
ENST00000371953.7:c.1055_1056delinsTT ENSP00000361021.3:p.Glu352Val
NM_000314.5:c.1055_1056delinsTT NP_000305.3:p.Glu352Val
NM_000314.6:c.1055_1056delinsTT NP_000305.3:p.Glu352Val
NM_001304717.2:c.1574_1575delinsTT NP_001291646.2:p.Glu525Val
NM_001304718.1:c.464_465delinsTT NP_001291647.1:p.Glu155Val
XM_006717926.2:c.1010_1011delinsTT XP_006717989.1:p.Glu337Val
XM_011539982.1:c.959_960delinsTT XP_011538284.1:p.Glu320Val
XR_945791.1:n.1625_1626delinsTT
NM_000314.7:c.1055_1056delinsTT NP_000305.3:p.Glu352Val
NM_001304717.5:c.1574_1575delinsTT NP_001291646.4:p.Glu525Val
NM_001304718.2:c.464_465delinsTT NP_001291647.1:p.Glu155Val
NM_000314.8:c.1055_1056delinsTT MANE Select NP_000305.3:p.Glu352Val