Canonical Allele Identifier: CA891837670
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965378_87965379delinsTT , CM000672.2:g.87965378_87965379delinsTT GRCh38
NC_000010.10:g.89725135_89725136delinsTT , CM000672.1:g.89725135_89725136delinsTT GRCh37
NC_000010.9:g.89715115_89715116delinsTT NCBI36
NG_007466.2:g.106940_106941delinsTT , LRG_311:g.106940_106941delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1211_1212delinsTT ENSP00000514759.2:p.Glu404Val
ENST00000710265.1:c.*147_*148delinsTT ENSP00000518161.1:n.*147_*148delinsTT
ENST00000688158.2:n.1853_1854delinsTT
ENST00000688922.2:c.*948_*949delinsTT ENSP00000508742.2:n.*948_*949delinsTT
ENST00000700021.1:c.1073_1074delinsTT ENSP00000514757.1:p.Glu358Val
ENST00000700022.1:c.*457_*458delinsTT ENSP00000514758.1:n.*457_*458delinsTT
ENST00000700023.1:n.2276_2277delinsTT
ENST00000700024.1:n.2510_2511delinsTT
ENST00000706954.1:c.1118_1119delinsTT ENSP00000516674.1:p.Glu373Val
ENST00000706955.1:c.*1153_*1154delinsTT ENSP00000516675.1:n.*1153_*1154delinsTT
ENST00000686459.1:c.*704_*705delinsTT ENSP00000508909.1:n.*704_*705delinsTT
ENST00000688158.1:c.*1229_*1230delinsTT ENSP00000509254.1:n.*1229_*1230delinsTT
ENST00000688308.1:c.1118_1119delinsTT ENSP00000508752.1:p.Glu373Val
ENST00000688922.1:c.1039_1040delinsTT
ENST00000693560.1:c.1637_1638delinsTT ENSP00000509861.1:p.Glu546Val
ENST00000371953.8:c.1118_1119delinsTT MANE Select ENSP00000361021.3:p.Glu373Val
ENST00000371953.7:c.1118_1119delinsTT ENSP00000361021.3:p.Glu373Val
NM_000314.5:c.1118_1119delinsTT NP_000305.3:p.Glu373Val
NM_000314.6:c.1118_1119delinsTT NP_000305.3:p.Glu373Val
NM_001304717.2:c.1637_1638delinsTT NP_001291646.2:p.Glu546Val
NM_001304718.1:c.527_528delinsTT NP_001291647.1:p.Glu176Val
XM_006717926.2:c.1073_1074delinsTT XP_006717989.1:p.Glu358Val
XM_011539982.1:c.1022_1023delinsTT XP_011538284.1:p.Glu341Val
XR_945791.1:n.1688_1689delinsTT
NM_000314.7:c.1118_1119delinsTT NP_000305.3:p.Glu373Val
NM_001304717.5:c.1637_1638delinsTT NP_001291646.4:p.Glu546Val
NM_001304718.2:c.527_528delinsTT NP_001291647.1:p.Glu176Val
NM_000314.8:c.1118_1119delinsTT MANE Select NP_000305.3:p.Glu373Val