Canonical Allele Identifier: CA891837102
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87933099_87933101delinsACT , CM000672.2:g.87933099_87933101delinsACT GRCh38
NC_000010.10:g.89692856_89692858delinsACT , CM000672.1:g.89692856_89692858delinsACT GRCh37
NC_000010.9:g.89682836_89682838delinsACT NCBI36
NG_007466.2:g.74661_74663delinsACT , LRG_311:g.74661_74663delinsACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.340_342delinsACT ENSP00000514759.2:p.Glu114Thr
ENST00000710265.1:c.340_342delinsACT ENSP00000518161.1:p.Glu114Thr
ENST00000472832.3:c.340_342delinsACT ENSP00000483066.2:p.Glu114Thr
ENST00000688158.2:n.1075_1077delinsACT
ENST00000688922.2:c.*170_*172delinsACT ENSP00000508742.2:n.*170_*172delinsACT
ENST00000700021.1:c.295_297delinsACT ENSP00000514757.1:p.Glu99Thr
ENST00000700022.1:c.340_342delinsACT ENSP00000514758.1:p.Glu114Thr
ENST00000700029.1:c.174_176delinsACT
ENST00000706954.1:c.340_342delinsACT ENSP00000516674.1:p.Glu114Thr
ENST00000706955.1:c.*375_*377delinsACT ENSP00000516675.1:n.*375_*377delinsACT
ENST00000686459.1:c.340_342delinsACT ENSP00000508909.1:p.Glu114Thr
ENST00000688158.1:c.*451_*453delinsACT ENSP00000509254.1:n.*451_*453delinsACT
ENST00000688308.1:c.340_342delinsACT ENSP00000508752.1:p.Glu114Thr
ENST00000688922.1:c.261_263delinsACT
ENST00000693560.1:c.859_861delinsACT ENSP00000509861.1:p.Glu287Thr
ENST00000371953.8:c.340_342delinsACT MANE Select ENSP00000361021.3:p.Glu114Thr
ENST00000371953.7:c.340_342delinsACT ENSP00000361021.3:p.Glu114Thr
ENST00000498703.1:n.166_168delinsACT
ENST00000610634.1:c.238_240delinsACT ENSP00000477517.1:p.Glu80Thr
NM_000314.5:c.340_342delinsACT NP_000305.3:p.Glu114Thr
NM_000314.6:c.340_342delinsACT NP_000305.3:p.Glu114Thr
NM_001304717.2:c.859_861delinsACT NP_001291646.2:p.Glu287Thr
NM_001304718.1:c.-411_-409delinsACT NP_001291647.1:n.-411_-409delinsACT
XM_006717926.2:c.295_297delinsACT XP_006717989.1:p.Glu99Thr
XM_011539981.1:c.340_342delinsACT XP_011538283.1:p.Glu114Thr
XM_011539982.1:c.244_246delinsACT XP_011538284.1:p.Glu82Thr
XR_945789.1:n.1052_1054delinsACT
XR_945790.1:n.1052_1054delinsACT
XR_945791.1:n.1052_1054delinsACT
NM_000314.7:c.340_342delinsACT NP_000305.3:p.Glu114Thr
NM_001304717.5:c.859_861delinsACT NP_001291646.4:p.Glu287Thr
NM_001304718.2:c.-411_-409delinsACT NP_001291647.1:n.-411_-409delinsACT
NM_000314.8:c.340_342delinsACT MANE Select NP_000305.3:p.Glu114Thr