Canonical Allele Identifier: CA891840776
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957945_87957946delinsCG , CM000672.2:g.87957945_87957946delinsCG GRCh38
NC_000010.10:g.89717702_89717703delinsCG , CM000672.1:g.89717702_89717703delinsCG GRCh37
NC_000010.9:g.89707682_89707683delinsCG NCBI36
NG_007466.2:g.99507_99508delinsCG , LRG_311:g.99507_99508delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.727_728delinsCG ENSP00000514759.2:p.Phe243Arg
ENST00000710265.1:c.727_728delinsCG ENSP00000518161.1:p.Phe243Arg
ENST00000472832.3:c.727_728delinsCG ENSP00000483066.2:p.Phe243Arg
ENST00000688158.2:n.1462_1463delinsCG
ENST00000688922.2:c.*557_*558delinsCG ENSP00000508742.2:n.*557_*558delinsCG
ENST00000700021.1:c.682_683delinsCG ENSP00000514757.1:p.Phe228Arg
ENST00000700022.1:c.*66_*67delinsCG ENSP00000514758.1:n.*66_*67delinsCG
ENST00000700023.1:n.1885_1886delinsCG
ENST00000700024.1:n.2119_2120delinsCG
ENST00000700025.1:n.1496_1497delinsCG
ENST00000700026.1:n.364_365delinsCG
ENST00000700029.1:c.561_562delinsCG
ENST00000706954.1:c.727_728delinsCG ENSP00000516674.1:p.Phe243Arg
ENST00000706955.1:c.*762_*763delinsCG ENSP00000516675.1:n.*762_*763delinsCG
ENST00000686459.1:c.*313_*314delinsCG ENSP00000508909.1:n.*313_*314delinsCG
ENST00000688158.1:c.*838_*839delinsCG ENSP00000509254.1:n.*838_*839delinsCG
ENST00000688308.1:c.727_728delinsCG ENSP00000508752.1:p.Phe243Arg
ENST00000688922.1:c.648_649delinsCG
ENST00000693560.1:c.1246_1247delinsCG ENSP00000509861.1:p.Phe416Arg
ENST00000371953.8:c.727_728delinsCG MANE Select ENSP00000361021.3:p.Phe243Arg
ENST00000371953.7:c.727_728delinsCG ENSP00000361021.3:p.Phe243Arg
ENST00000472832.2:c.154_155delinsCG ENSP00000483066.1:p.Phe52Arg
NM_000314.5:c.727_728delinsCG NP_000305.3:p.Phe243Arg
NM_000314.6:c.727_728delinsCG NP_000305.3:p.Phe243Arg
NM_001304717.2:c.1246_1247delinsCG NP_001291646.2:p.Phe416Arg
NM_001304718.1:c.136_137delinsCG NP_001291647.1:p.Phe46Arg
XM_006717926.2:c.682_683delinsCG XP_006717989.1:p.Phe228Arg
XM_011539981.1:c.727_728delinsCG XP_011538283.1:p.Phe243Arg
XM_011539982.1:c.631_632delinsCG XP_011538284.1:p.Phe211Arg
XR_945791.1:n.1297_1298delinsCG
NM_000314.7:c.727_728delinsCG NP_000305.3:p.Phe243Arg
NM_001304717.5:c.1246_1247delinsCG NP_001291646.4:p.Phe416Arg
NM_001304718.2:c.136_137delinsCG NP_001291647.1:p.Phe46Arg
NM_000314.8:c.727_728delinsCG MANE Select NP_000305.3:p.Phe243Arg