Canonical Allele Identifier: CA891839775
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957945_87957947delinsATT , CM000672.2:g.87957945_87957947delinsATT GRCh38
NC_000010.10:g.89717702_89717704delinsATT , CM000672.1:g.89717702_89717704delinsATT GRCh37
NC_000010.9:g.89707682_89707684delinsATT NCBI36
NG_007466.2:g.99507_99509delinsATT , LRG_311:g.99507_99509delinsATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.727_729delinsATT ENSP00000514759.2:p.Phe243Ile
ENST00000710265.1:c.727_729delinsATT ENSP00000518161.1:p.Phe243Ile
ENST00000472832.3:c.727_729delinsATT ENSP00000483066.2:p.Phe243Ile
ENST00000688158.2:n.1462_1464delinsATT
ENST00000688922.2:c.*557_*559delinsATT ENSP00000508742.2:n.*557_*559delinsATT
ENST00000700021.1:c.682_684delinsATT ENSP00000514757.1:p.Phe228Ile
ENST00000700022.1:c.*66_*68delinsATT ENSP00000514758.1:n.*66_*68delinsATT
ENST00000700023.1:n.1885_1887delinsATT
ENST00000700024.1:n.2119_2121delinsATT
ENST00000700025.1:n.1496_1498delinsATT
ENST00000700026.1:n.364_366delinsATT
ENST00000700029.1:c.561_563delinsATT
ENST00000706954.1:c.727_729delinsATT ENSP00000516674.1:p.Phe243Ile
ENST00000706955.1:c.*762_*764delinsATT ENSP00000516675.1:n.*762_*764delinsATT
ENST00000686459.1:c.*313_*315delinsATT ENSP00000508909.1:n.*313_*315delinsATT
ENST00000688158.1:c.*838_*840delinsATT ENSP00000509254.1:n.*838_*840delinsATT
ENST00000688308.1:c.727_729delinsATT ENSP00000508752.1:p.Phe243Ile
ENST00000688922.1:c.648_650delinsATT
ENST00000693560.1:c.1246_1248delinsATT ENSP00000509861.1:p.Phe416Ile
ENST00000371953.8:c.727_729delinsATT MANE Select ENSP00000361021.3:p.Phe243Ile
ENST00000371953.7:c.727_729delinsATT ENSP00000361021.3:p.Phe243Ile
ENST00000472832.2:c.154_156delinsATT ENSP00000483066.1:p.Phe52Ile
NM_000314.5:c.727_729delinsATT NP_000305.3:p.Phe243Ile
NM_000314.6:c.727_729delinsATT NP_000305.3:p.Phe243Ile
NM_001304717.2:c.1246_1248delinsATT NP_001291646.2:p.Phe416Ile
NM_001304718.1:c.136_138delinsATT NP_001291647.1:p.Phe46Ile
XM_006717926.2:c.682_684delinsATT XP_006717989.1:p.Phe228Ile
XM_011539981.1:c.727_729delinsATT XP_011538283.1:p.Phe243Ile
XM_011539982.1:c.631_633delinsATT XP_011538284.1:p.Phe211Ile
XR_945791.1:n.1297_1299delinsATT
NM_000314.7:c.727_729delinsATT NP_000305.3:p.Phe243Ile
NM_001304717.5:c.1246_1248delinsATT NP_001291646.4:p.Phe416Ile
NM_001304718.2:c.136_138delinsATT NP_001291647.1:p.Phe46Ile
NM_000314.8:c.727_729delinsATT MANE Select NP_000305.3:p.Phe243Ile