Canonical Allele Identifier: CA2579926379
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965465_87965466delinsCT , CM000672.2:g.87965465_87965466delinsCT GRCh38
NC_000010.10:g.89725222_89725223delinsCT , CM000672.1:g.89725222_89725223delinsCT GRCh37
NC_000010.9:g.89715202_89715203delinsCT NCBI36
NG_007466.2:g.107027_107028delinsCT , LRG_311:g.107027_107028delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1298_1299delinsCT ENSP00000514759.2:p.Lys433Thr
ENST00000710265.1:c.*234_*235delinsCT ENSP00000518161.1:n.*234_*235delinsCT
ENST00000688158.2:n.1940_1941delinsCT
ENST00000688922.2:c.*1035_*1036delinsCT ENSP00000508742.2:n.*1035_*1036delinsCT
ENST00000700021.1:c.1160_1161delinsCT ENSP00000514757.1:p.Lys387Thr
ENST00000700022.1:c.*544_*545delinsCT ENSP00000514758.1:n.*544_*545delinsCT
ENST00000700023.1:n.2363_2364delinsCT
ENST00000700024.1:n.2597_2598delinsCT
ENST00000706954.1:c.1205_1206delinsCT ENSP00000516674.1:p.Lys402Thr
ENST00000706955.1:c.*1240_*1241delinsCT ENSP00000516675.1:n.*1240_*1241delinsCT
ENST00000686459.1:c.*791_*792delinsCT ENSP00000508909.1:n.*791_*792delinsCT
ENST00000688158.1:c.*1316_*1317delinsCT ENSP00000509254.1:n.*1316_*1317delinsCT
ENST00000688308.1:c.1205_1206delinsCT ENSP00000508752.1:p.Lys402Thr
ENST00000688922.1:c.1126_1127delinsCT
ENST00000693560.1:c.1724_1725delinsCT ENSP00000509861.1:p.Lys575Thr
ENST00000371953.8:c.1205_1206delinsCT MANE Select ENSP00000361021.3:p.Lys402Thr
ENST00000371953.7:c.1205_1206delinsCT ENSP00000361021.3:p.Lys402Thr
NM_000314.5:c.1205_1206delinsCT NP_000305.3:p.Lys402Thr
NM_000314.6:c.1205_1206delinsCT NP_000305.3:p.Lys402Thr
NM_001304717.2:c.1724_1725delinsCT NP_001291646.2:p.Lys575Thr
NM_001304718.1:c.614_615delinsCT NP_001291647.1:p.Lys205Thr
XM_006717926.2:c.1160_1161delinsCT XP_006717989.1:p.Lys387Thr
XM_011539982.1:c.1109_1110delinsCT XP_011538284.1:p.Lys370Thr
XR_945791.1:n.1775_1776delinsCT
NM_000314.7:c.1205_1206delinsCT NP_000305.3:p.Lys402Thr
NM_001304717.5:c.1724_1725delinsCT NP_001291646.4:p.Lys575Thr
NM_001304718.2:c.614_615delinsCT NP_001291647.1:p.Lys205Thr
NM_000314.8:c.1205_1206delinsCT MANE Select NP_000305.3:p.Lys402Thr