Canonical Allele Identifier: CA891839803
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957951_87957953delinsACT , CM000672.2:g.87957951_87957953delinsACT GRCh38
NC_000010.10:g.89717708_89717710delinsACT , CM000672.1:g.89717708_89717710delinsACT GRCh37
NC_000010.9:g.89707688_89707690delinsACT NCBI36
NG_007466.2:g.99513_99515delinsACT , LRG_311:g.99513_99515delinsACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.733_735delinsACT ENSP00000514759.2:p.Gln245Thr
ENST00000710265.1:c.733_735delinsACT ENSP00000518161.1:p.Gln245Thr
ENST00000472832.3:c.733_735delinsACT ENSP00000483066.2:p.Gln245Thr
ENST00000688158.2:n.1468_1470delinsACT
ENST00000688922.2:c.*563_*565delinsACT ENSP00000508742.2:n.*563_*565delinsACT
ENST00000700021.1:c.688_690delinsACT ENSP00000514757.1:p.Gln230Thr
ENST00000700022.1:c.*72_*74delinsACT ENSP00000514758.1:n.*72_*74delinsACT
ENST00000700023.1:n.1891_1893delinsACT
ENST00000700024.1:n.2125_2127delinsACT
ENST00000700025.1:n.1502_1504delinsACT
ENST00000700026.1:n.370_372delinsACT
ENST00000700029.1:c.567_569delinsACT
ENST00000706954.1:c.733_735delinsACT ENSP00000516674.1:p.Gln245Thr
ENST00000706955.1:c.*768_*770delinsACT ENSP00000516675.1:n.*768_*770delinsACT
ENST00000686459.1:c.*319_*321delinsACT ENSP00000508909.1:n.*319_*321delinsACT
ENST00000688158.1:c.*844_*846delinsACT ENSP00000509254.1:n.*844_*846delinsACT
ENST00000688308.1:c.733_735delinsACT ENSP00000508752.1:p.Gln245Thr
ENST00000688922.1:c.654_656delinsACT
ENST00000693560.1:c.1252_1254delinsACT ENSP00000509861.1:p.Gln418Thr
ENST00000371953.8:c.733_735delinsACT MANE Select ENSP00000361021.3:p.Gln245Thr
ENST00000371953.7:c.733_735delinsACT ENSP00000361021.3:p.Gln245Thr
ENST00000472832.2:c.160_162delinsACT ENSP00000483066.1:p.Gln54Thr
NM_000314.5:c.733_735delinsACT NP_000305.3:p.Gln245Thr
NM_000314.6:c.733_735delinsACT NP_000305.3:p.Gln245Thr
NM_001304717.2:c.1252_1254delinsACT NP_001291646.2:p.Gln418Thr
NM_001304718.1:c.142_144delinsACT NP_001291647.1:p.Gln48Thr
XM_006717926.2:c.688_690delinsACT XP_006717989.1:p.Gln230Thr
XM_011539981.1:c.733_735delinsACT XP_011538283.1:p.Gln245Thr
XM_011539982.1:c.637_639delinsACT XP_011538284.1:p.Gln213Thr
XR_945791.1:n.1303_1305delinsACT
NM_000314.7:c.733_735delinsACT NP_000305.3:p.Gln245Thr
NM_001304717.5:c.1252_1254delinsACT NP_001291646.4:p.Gln418Thr
NM_001304718.2:c.142_144delinsACT NP_001291647.1:p.Gln48Thr
NM_000314.8:c.733_735delinsACT MANE Select NP_000305.3:p.Gln245Thr