Canonical Allele Identifier: CA891839773
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957945_87957947delinsACT , CM000672.2:g.87957945_87957947delinsACT GRCh38
NC_000010.10:g.89717702_89717704delinsACT , CM000672.1:g.89717702_89717704delinsACT GRCh37
NC_000010.9:g.89707682_89707684delinsACT NCBI36
NG_007466.2:g.99507_99509delinsACT , LRG_311:g.99507_99509delinsACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.727_729delinsACT ENSP00000514759.2:p.Phe243Thr
ENST00000710265.1:c.727_729delinsACT ENSP00000518161.1:p.Phe243Thr
ENST00000472832.3:c.727_729delinsACT ENSP00000483066.2:p.Phe243Thr
ENST00000688158.2:n.1462_1464delinsACT
ENST00000688922.2:c.*557_*559delinsACT ENSP00000508742.2:n.*557_*559delinsACT
ENST00000700021.1:c.682_684delinsACT ENSP00000514757.1:p.Phe228Thr
ENST00000700022.1:c.*66_*68delinsACT ENSP00000514758.1:n.*66_*68delinsACT
ENST00000700023.1:n.1885_1887delinsACT
ENST00000700024.1:n.2119_2121delinsACT
ENST00000700025.1:n.1496_1498delinsACT
ENST00000700026.1:n.364_366delinsACT
ENST00000700029.1:c.561_563delinsACT
ENST00000706954.1:c.727_729delinsACT ENSP00000516674.1:p.Phe243Thr
ENST00000706955.1:c.*762_*764delinsACT ENSP00000516675.1:n.*762_*764delinsACT
ENST00000686459.1:c.*313_*315delinsACT ENSP00000508909.1:n.*313_*315delinsACT
ENST00000688158.1:c.*838_*840delinsACT ENSP00000509254.1:n.*838_*840delinsACT
ENST00000688308.1:c.727_729delinsACT ENSP00000508752.1:p.Phe243Thr
ENST00000688922.1:c.648_650delinsACT
ENST00000693560.1:c.1246_1248delinsACT ENSP00000509861.1:p.Phe416Thr
ENST00000371953.8:c.727_729delinsACT MANE Select ENSP00000361021.3:p.Phe243Thr
ENST00000371953.7:c.727_729delinsACT ENSP00000361021.3:p.Phe243Thr
ENST00000472832.2:c.154_156delinsACT ENSP00000483066.1:p.Phe52Thr
NM_000314.5:c.727_729delinsACT NP_000305.3:p.Phe243Thr
NM_000314.6:c.727_729delinsACT NP_000305.3:p.Phe243Thr
NM_001304717.2:c.1246_1248delinsACT NP_001291646.2:p.Phe416Thr
NM_001304718.1:c.136_138delinsACT NP_001291647.1:p.Phe46Thr
XM_006717926.2:c.682_684delinsACT XP_006717989.1:p.Phe228Thr
XM_011539981.1:c.727_729delinsACT XP_011538283.1:p.Phe243Thr
XM_011539982.1:c.631_633delinsACT XP_011538284.1:p.Phe211Thr
XR_945791.1:n.1297_1299delinsACT
NM_000314.7:c.727_729delinsACT NP_000305.3:p.Phe243Thr
NM_001304717.5:c.1246_1248delinsACT NP_001291646.4:p.Phe416Thr
NM_001304718.2:c.136_138delinsACT NP_001291647.1:p.Phe46Thr
NM_000314.8:c.727_729delinsACT MANE Select NP_000305.3:p.Phe243Thr