Canonical Allele Identifier: CA891837662
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965377_87965379delinsTTT , CM000672.2:g.87965377_87965379delinsTTT GRCh38
NC_000010.10:g.89725134_89725136delinsTTT , CM000672.1:g.89725134_89725136delinsTTT GRCh37
NC_000010.9:g.89715114_89715116delinsTTT NCBI36
NG_007466.2:g.106939_106941delinsTTT , LRG_311:g.106939_106941delinsTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1210_1212delinsTTT ENSP00000514759.2:p.Glu404Phe
ENST00000710265.1:c.*146_*148delinsTTT ENSP00000518161.1:n.*146_*148delinsTTT
ENST00000688158.2:n.1852_1854delinsTTT
ENST00000688922.2:c.*947_*949delinsTTT ENSP00000508742.2:n.*947_*949delinsTTT
ENST00000700021.1:c.1072_1074delinsTTT ENSP00000514757.1:p.Glu358Phe
ENST00000700022.1:c.*456_*458delinsTTT ENSP00000514758.1:n.*456_*458delinsTTT
ENST00000700023.1:n.2275_2277delinsTTT
ENST00000700024.1:n.2509_2511delinsTTT
ENST00000706954.1:c.1117_1119delinsTTT ENSP00000516674.1:p.Glu373Phe
ENST00000706955.1:c.*1152_*1154delinsTTT ENSP00000516675.1:n.*1152_*1154delinsTTT
ENST00000686459.1:c.*703_*705delinsTTT ENSP00000508909.1:n.*703_*705delinsTTT
ENST00000688158.1:c.*1228_*1230delinsTTT ENSP00000509254.1:n.*1228_*1230delinsTTT
ENST00000688308.1:c.1117_1119delinsTTT ENSP00000508752.1:p.Glu373Phe
ENST00000688922.1:c.1038_1040delinsTTT
ENST00000693560.1:c.1636_1638delinsTTT ENSP00000509861.1:p.Glu546Phe
ENST00000371953.8:c.1117_1119delinsTTT MANE Select ENSP00000361021.3:p.Glu373Phe
ENST00000371953.7:c.1117_1119delinsTTT ENSP00000361021.3:p.Glu373Phe
NM_000314.5:c.1117_1119delinsTTT NP_000305.3:p.Glu373Phe
NM_000314.6:c.1117_1119delinsTTT NP_000305.3:p.Glu373Phe
NM_001304717.2:c.1636_1638delinsTTT NP_001291646.2:p.Glu546Phe
NM_001304718.1:c.526_528delinsTTT NP_001291647.1:p.Glu176Phe
XM_006717926.2:c.1072_1074delinsTTT XP_006717989.1:p.Glu358Phe
XM_011539982.1:c.1021_1023delinsTTT XP_011538284.1:p.Glu341Phe
XR_945791.1:n.1687_1689delinsTTT
NM_000314.7:c.1117_1119delinsTTT NP_000305.3:p.Glu373Phe
NM_001304717.5:c.1636_1638delinsTTT NP_001291646.4:p.Glu546Phe
NM_001304718.2:c.526_528delinsTTT NP_001291647.1:p.Glu176Phe
NM_000314.8:c.1117_1119delinsTTT MANE Select NP_000305.3:p.Glu373Phe