Canonical Allele Identifier: CA891840118
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958014_87958016delinsGGT , CM000672.2:g.87958014_87958016delinsGGT GRCh38
NC_000010.10:g.89717771_89717773delinsGGT , CM000672.1:g.89717771_89717773delinsGGT GRCh37
NC_000010.9:g.89707751_89707753delinsGGT NCBI36
NG_007466.2:g.99576_99578delinsGGT , LRG_311:g.99576_99578delinsGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.796_798delinsGGT ENSP00000514759.2:p.Lys266Gly
ENST00000710265.1:c.796_798delinsGGT ENSP00000518161.1:p.Lys266Gly
ENST00000472832.3:c.796_798delinsGGT ENSP00000483066.2:p.Lys266Gly
ENST00000688158.2:n.1531_1533delinsGGT
ENST00000688922.2:c.*626_*628delinsGGT ENSP00000508742.2:n.*626_*628delinsGGT
ENST00000700021.1:c.751_753delinsGGT ENSP00000514757.1:p.Lys251Gly
ENST00000700022.1:c.*135_*137delinsGGT ENSP00000514758.1:n.*135_*137delinsGGT
ENST00000700023.1:n.1954_1956delinsGGT
ENST00000700024.1:n.2188_2190delinsGGT
ENST00000700025.1:n.1565_1567delinsGGT
ENST00000700026.1:n.433_435delinsGGT
ENST00000700029.1:c.630_632delinsGGT
ENST00000706954.1:c.796_798delinsGGT ENSP00000516674.1:p.Lys266Gly
ENST00000706955.1:c.*831_*833delinsGGT ENSP00000516675.1:n.*831_*833delinsGGT
ENST00000686459.1:c.*382_*384delinsGGT ENSP00000508909.1:n.*382_*384delinsGGT
ENST00000688158.1:c.*907_*909delinsGGT ENSP00000509254.1:n.*907_*909delinsGGT
ENST00000688308.1:c.796_798delinsGGT ENSP00000508752.1:p.Lys266Gly
ENST00000688922.1:c.717_719delinsGGT
ENST00000693560.1:c.1315_1317delinsGGT ENSP00000509861.1:p.Lys439Gly
ENST00000371953.8:c.796_798delinsGGT MANE Select ENSP00000361021.3:p.Lys266Gly
ENST00000371953.7:c.796_798delinsGGT ENSP00000361021.3:p.Lys266Gly
ENST00000472832.2:c.223_225delinsGGT ENSP00000483066.1:p.Lys75Gly
NM_000314.5:c.796_798delinsGGT NP_000305.3:p.Lys266Gly
NM_000314.6:c.796_798delinsGGT NP_000305.3:p.Lys266Gly
NM_001304717.2:c.1315_1317delinsGGT NP_001291646.2:p.Lys439Gly
NM_001304718.1:c.205_207delinsGGT NP_001291647.1:p.Lys69Gly
XM_006717926.2:c.751_753delinsGGT XP_006717989.1:p.Lys251Gly
XM_011539981.1:c.796_798delinsGGT XP_011538283.1:p.Lys266Gly
XM_011539982.1:c.700_702delinsGGT XP_011538284.1:p.Lys234Gly
XR_945791.1:n.1366_1368delinsGGT
NM_000314.7:c.796_798delinsGGT NP_000305.3:p.Lys266Gly
NM_001304717.5:c.1315_1317delinsGGT NP_001291646.4:p.Lys439Gly
NM_001304718.2:c.205_207delinsGGT NP_001291647.1:p.Lys69Gly
NM_000314.8:c.796_798delinsGGT MANE Select NP_000305.3:p.Lys266Gly