Canonical Allele Identifier: CA891841702
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965452_87965453delinsGG , CM000672.2:g.87965452_87965453delinsGG GRCh38
NC_000010.10:g.89725209_89725210delinsGG , CM000672.1:g.89725209_89725210delinsGG GRCh37
NC_000010.9:g.89715189_89715190delinsGG NCBI36
NG_007466.2:g.107014_107015delinsGG , LRG_311:g.107014_107015delinsGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1285_1286delinsGG ENSP00000514759.2:p.Thr429Gly
ENST00000710265.1:c.*221_*222delinsGG ENSP00000518161.1:n.*221_*222delinsGG
ENST00000688158.2:n.1927_1928delinsGG
ENST00000688922.2:c.*1022_*1023delinsGG ENSP00000508742.2:n.*1022_*1023delinsGG
ENST00000700021.1:c.1147_1148delinsGG ENSP00000514757.1:p.Thr383Gly
ENST00000700022.1:c.*531_*532delinsGG ENSP00000514758.1:n.*531_*532delinsGG
ENST00000700023.1:n.2350_2351delinsGG
ENST00000700024.1:n.2584_2585delinsGG
ENST00000706954.1:c.1192_1193delinsGG ENSP00000516674.1:p.Thr398Gly
ENST00000706955.1:c.*1227_*1228delinsGG ENSP00000516675.1:n.*1227_*1228delinsGG
ENST00000686459.1:c.*778_*779delinsGG ENSP00000508909.1:n.*778_*779delinsGG
ENST00000688158.1:c.*1303_*1304delinsGG ENSP00000509254.1:n.*1303_*1304delinsGG
ENST00000688308.1:c.1192_1193delinsGG ENSP00000508752.1:p.Thr398Gly
ENST00000688922.1:c.1113_1114delinsGG
ENST00000693560.1:c.1711_1712delinsGG ENSP00000509861.1:p.Thr571Gly
ENST00000371953.8:c.1192_1193delinsGG MANE Select ENSP00000361021.3:p.Thr398Gly
ENST00000371953.7:c.1192_1193delinsGG ENSP00000361021.3:p.Thr398Gly
NM_000314.5:c.1192_1193delinsGG NP_000305.3:p.Thr398Gly
NM_000314.6:c.1192_1193delinsGG NP_000305.3:p.Thr398Gly
NM_001304717.2:c.1711_1712delinsGG NP_001291646.2:p.Thr571Gly
NM_001304718.1:c.601_602delinsGG NP_001291647.1:p.Thr201Gly
XM_006717926.2:c.1147_1148delinsGG XP_006717989.1:p.Thr383Gly
XM_011539982.1:c.1096_1097delinsGG XP_011538284.1:p.Thr366Gly
XR_945791.1:n.1762_1763delinsGG
NM_000314.7:c.1192_1193delinsGG NP_000305.3:p.Thr398Gly
NM_001304717.5:c.1711_1712delinsGG NP_001291646.4:p.Thr571Gly
NM_001304718.2:c.601_602delinsGG NP_001291647.1:p.Thr201Gly
NM_000314.8:c.1192_1193delinsGG MANE Select NP_000305.3:p.Thr398Gly