Canonical Allele Identifier: CA891837263
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965332_87965334delinsTAT , CM000672.2:g.87965332_87965334delinsTAT GRCh38
NC_000010.10:g.89725089_89725091delinsTAT , CM000672.1:g.89725089_89725091delinsTAT GRCh37
NC_000010.9:g.89715069_89715071delinsTAT NCBI36
NG_007466.2:g.106894_106896delinsTAT , LRG_311:g.106894_106896delinsTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1165_1167delinsTAT ENSP00000514759.2:p.Glu389Tyr
ENST00000710265.1:c.*101_*103delinsTAT ENSP00000518161.1:n.*101_*103delinsTAT
ENST00000688158.2:n.1807_1809delinsTAT
ENST00000688922.2:c.*902_*904delinsTAT ENSP00000508742.2:n.*902_*904delinsTAT
ENST00000700021.1:c.1027_1029delinsTAT ENSP00000514757.1:p.Glu343Tyr
ENST00000700022.1:c.*411_*413delinsTAT ENSP00000514758.1:n.*411_*413delinsTAT
ENST00000700023.1:n.2230_2232delinsTAT
ENST00000700024.1:n.2464_2466delinsTAT
ENST00000706954.1:c.1072_1074delinsTAT ENSP00000516674.1:p.Glu358Tyr
ENST00000706955.1:c.*1107_*1109delinsTAT ENSP00000516675.1:n.*1107_*1109delinsTAT
ENST00000686459.1:c.*658_*660delinsTAT ENSP00000508909.1:n.*658_*660delinsTAT
ENST00000688158.1:c.*1183_*1185delinsTAT ENSP00000509254.1:n.*1183_*1185delinsTAT
ENST00000688308.1:c.1072_1074delinsTAT ENSP00000508752.1:p.Glu358Tyr
ENST00000688922.1:c.993_995delinsTAT
ENST00000693560.1:c.1591_1593delinsTAT ENSP00000509861.1:p.Glu531Tyr
ENST00000371953.8:c.1072_1074delinsTAT MANE Select ENSP00000361021.3:p.Glu358Tyr
ENST00000371953.7:c.1072_1074delinsTAT ENSP00000361021.3:p.Glu358Tyr
NM_000314.5:c.1072_1074delinsTAT NP_000305.3:p.Glu358Tyr
NM_000314.6:c.1072_1074delinsTAT NP_000305.3:p.Glu358Tyr
NM_001304717.2:c.1591_1593delinsTAT NP_001291646.2:p.Glu531Tyr
NM_001304718.1:c.481_483delinsTAT NP_001291647.1:p.Glu161Tyr
XM_006717926.2:c.1027_1029delinsTAT XP_006717989.1:p.Glu343Tyr
XM_011539982.1:c.976_978delinsTAT XP_011538284.1:p.Glu326Tyr
XR_945791.1:n.1642_1644delinsTAT
NM_000314.7:c.1072_1074delinsTAT NP_000305.3:p.Glu358Tyr
NM_001304717.5:c.1591_1593delinsTAT NP_001291646.4:p.Glu531Tyr
NM_001304718.2:c.481_483delinsTAT NP_001291647.1:p.Glu161Tyr
NM_000314.8:c.1072_1074delinsTAT MANE Select NP_000305.3:p.Glu358Tyr