Canonical Allele Identifier: CA891837663
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965377_87965379delinsTCT , CM000672.2:g.87965377_87965379delinsTCT GRCh38
NC_000010.10:g.89725134_89725136delinsTCT , CM000672.1:g.89725134_89725136delinsTCT GRCh37
NC_000010.9:g.89715114_89715116delinsTCT NCBI36
NG_007466.2:g.106939_106941delinsTCT , LRG_311:g.106939_106941delinsTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1210_1212delinsTCT ENSP00000514759.2:p.Glu404Ser
ENST00000710265.1:c.*146_*148delinsTCT ENSP00000518161.1:n.*146_*148delinsTCT
ENST00000688158.2:n.1852_1854delinsTCT
ENST00000688922.2:c.*947_*949delinsTCT ENSP00000508742.2:n.*947_*949delinsTCT
ENST00000700021.1:c.1072_1074delinsTCT ENSP00000514757.1:p.Glu358Ser
ENST00000700022.1:c.*456_*458delinsTCT ENSP00000514758.1:n.*456_*458delinsTCT
ENST00000700023.1:n.2275_2277delinsTCT
ENST00000700024.1:n.2509_2511delinsTCT
ENST00000706954.1:c.1117_1119delinsTCT ENSP00000516674.1:p.Glu373Ser
ENST00000706955.1:c.*1152_*1154delinsTCT ENSP00000516675.1:n.*1152_*1154delinsTCT
ENST00000686459.1:c.*703_*705delinsTCT ENSP00000508909.1:n.*703_*705delinsTCT
ENST00000688158.1:c.*1228_*1230delinsTCT ENSP00000509254.1:n.*1228_*1230delinsTCT
ENST00000688308.1:c.1117_1119delinsTCT ENSP00000508752.1:p.Glu373Ser
ENST00000688922.1:c.1038_1040delinsTCT
ENST00000693560.1:c.1636_1638delinsTCT ENSP00000509861.1:p.Glu546Ser
ENST00000371953.8:c.1117_1119delinsTCT MANE Select ENSP00000361021.3:p.Glu373Ser
ENST00000371953.7:c.1117_1119delinsTCT ENSP00000361021.3:p.Glu373Ser
NM_000314.5:c.1117_1119delinsTCT NP_000305.3:p.Glu373Ser
NM_000314.6:c.1117_1119delinsTCT NP_000305.3:p.Glu373Ser
NM_001304717.2:c.1636_1638delinsTCT NP_001291646.2:p.Glu546Ser
NM_001304718.1:c.526_528delinsTCT NP_001291647.1:p.Glu176Ser
XM_006717926.2:c.1072_1074delinsTCT XP_006717989.1:p.Glu358Ser
XM_011539982.1:c.1021_1023delinsTCT XP_011538284.1:p.Glu341Ser
XR_945791.1:n.1687_1689delinsTCT
NM_000314.7:c.1117_1119delinsTCT NP_000305.3:p.Glu373Ser
NM_001304717.5:c.1636_1638delinsTCT NP_001291646.4:p.Glu546Ser
NM_001304718.2:c.526_528delinsTCT NP_001291647.1:p.Glu176Ser
NM_000314.8:c.1117_1119delinsTCT MANE Select NP_000305.3:p.Glu373Ser