Canonical Allele Identifier: CA891837654
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965377_87965379delinsACT , CM000672.2:g.87965377_87965379delinsACT GRCh38
NC_000010.10:g.89725134_89725136delinsACT , CM000672.1:g.89725134_89725136delinsACT GRCh37
NC_000010.9:g.89715114_89715116delinsACT NCBI36
NG_007466.2:g.106939_106941delinsACT , LRG_311:g.106939_106941delinsACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1210_1212delinsACT ENSP00000514759.2:p.Glu404Thr
ENST00000710265.1:c.*146_*148delinsACT ENSP00000518161.1:n.*146_*148delinsACT
ENST00000688158.2:n.1852_1854delinsACT
ENST00000688922.2:c.*947_*949delinsACT ENSP00000508742.2:n.*947_*949delinsACT
ENST00000700021.1:c.1072_1074delinsACT ENSP00000514757.1:p.Glu358Thr
ENST00000700022.1:c.*456_*458delinsACT ENSP00000514758.1:n.*456_*458delinsACT
ENST00000700023.1:n.2275_2277delinsACT
ENST00000700024.1:n.2509_2511delinsACT
ENST00000706954.1:c.1117_1119delinsACT ENSP00000516674.1:p.Glu373Thr
ENST00000706955.1:c.*1152_*1154delinsACT ENSP00000516675.1:n.*1152_*1154delinsACT
ENST00000686459.1:c.*703_*705delinsACT ENSP00000508909.1:n.*703_*705delinsACT
ENST00000688158.1:c.*1228_*1230delinsACT ENSP00000509254.1:n.*1228_*1230delinsACT
ENST00000688308.1:c.1117_1119delinsACT ENSP00000508752.1:p.Glu373Thr
ENST00000688922.1:c.1038_1040delinsACT
ENST00000693560.1:c.1636_1638delinsACT ENSP00000509861.1:p.Glu546Thr
ENST00000371953.8:c.1117_1119delinsACT MANE Select ENSP00000361021.3:p.Glu373Thr
ENST00000371953.7:c.1117_1119delinsACT ENSP00000361021.3:p.Glu373Thr
NM_000314.5:c.1117_1119delinsACT NP_000305.3:p.Glu373Thr
NM_000314.6:c.1117_1119delinsACT NP_000305.3:p.Glu373Thr
NM_001304717.2:c.1636_1638delinsACT NP_001291646.2:p.Glu546Thr
NM_001304718.1:c.526_528delinsACT NP_001291647.1:p.Glu176Thr
XM_006717926.2:c.1072_1074delinsACT XP_006717989.1:p.Glu358Thr
XM_011539982.1:c.1021_1023delinsACT XP_011538284.1:p.Glu341Thr
XR_945791.1:n.1687_1689delinsACT
NM_000314.7:c.1117_1119delinsACT NP_000305.3:p.Glu373Thr
NM_001304717.5:c.1636_1638delinsACT NP_001291646.4:p.Glu546Thr
NM_001304718.2:c.526_528delinsACT NP_001291647.1:p.Glu176Thr
NM_000314.8:c.1117_1119delinsACT MANE Select NP_000305.3:p.Glu373Thr