Canonical Allele Identifier: CA891840775
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957945_87957946delinsGA , CM000672.2:g.87957945_87957946delinsGA GRCh38
NC_000010.10:g.89717702_89717703delinsGA , CM000672.1:g.89717702_89717703delinsGA GRCh37
NC_000010.9:g.89707682_89707683delinsGA NCBI36
NG_007466.2:g.99507_99508delinsGA , LRG_311:g.99507_99508delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.727_728delinsGA ENSP00000514759.2:p.Phe243Asp
ENST00000710265.1:c.727_728delinsGA ENSP00000518161.1:p.Phe243Asp
ENST00000472832.3:c.727_728delinsGA ENSP00000483066.2:p.Phe243Asp
ENST00000688158.2:n.1462_1463delinsGA
ENST00000688922.2:c.*557_*558delinsGA ENSP00000508742.2:n.*557_*558delinsGA
ENST00000700021.1:c.682_683delinsGA ENSP00000514757.1:p.Phe228Asp
ENST00000700022.1:c.*66_*67delinsGA ENSP00000514758.1:n.*66_*67delinsGA
ENST00000700023.1:n.1885_1886delinsGA
ENST00000700024.1:n.2119_2120delinsGA
ENST00000700025.1:n.1496_1497delinsGA
ENST00000700026.1:n.364_365delinsGA
ENST00000700029.1:c.561_562delinsGA
ENST00000706954.1:c.727_728delinsGA ENSP00000516674.1:p.Phe243Asp
ENST00000706955.1:c.*762_*763delinsGA ENSP00000516675.1:n.*762_*763delinsGA
ENST00000686459.1:c.*313_*314delinsGA ENSP00000508909.1:n.*313_*314delinsGA
ENST00000688158.1:c.*838_*839delinsGA ENSP00000509254.1:n.*838_*839delinsGA
ENST00000688308.1:c.727_728delinsGA ENSP00000508752.1:p.Phe243Asp
ENST00000688922.1:c.648_649delinsGA
ENST00000693560.1:c.1246_1247delinsGA ENSP00000509861.1:p.Phe416Asp
ENST00000371953.8:c.727_728delinsGA MANE Select ENSP00000361021.3:p.Phe243Asp
ENST00000371953.7:c.727_728delinsGA ENSP00000361021.3:p.Phe243Asp
ENST00000472832.2:c.154_155delinsGA ENSP00000483066.1:p.Phe52Asp
NM_000314.5:c.727_728delinsGA NP_000305.3:p.Phe243Asp
NM_000314.6:c.727_728delinsGA NP_000305.3:p.Phe243Asp
NM_001304717.2:c.1246_1247delinsGA NP_001291646.2:p.Phe416Asp
NM_001304718.1:c.136_137delinsGA NP_001291647.1:p.Phe46Asp
XM_006717926.2:c.682_683delinsGA XP_006717989.1:p.Phe228Asp
XM_011539981.1:c.727_728delinsGA XP_011538283.1:p.Phe243Asp
XM_011539982.1:c.631_632delinsGA XP_011538284.1:p.Phe211Asp
XR_945791.1:n.1297_1298delinsGA
NM_000314.7:c.727_728delinsGA NP_000305.3:p.Phe243Asp
NM_001304717.5:c.1246_1247delinsGA NP_001291646.4:p.Phe416Asp
NM_001304718.2:c.136_137delinsGA NP_001291647.1:p.Phe46Asp
NM_000314.8:c.727_728delinsGA MANE Select NP_000305.3:p.Phe243Asp