Canonical Allele Identifier: CA891838062
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965429_87965430delinsTT , CM000672.2:g.87965429_87965430delinsTT GRCh38
NC_000010.10:g.89725186_89725187delinsTT , CM000672.1:g.89725186_89725187delinsTT GRCh37
NC_000010.9:g.89715166_89715167delinsTT NCBI36
NG_007466.2:g.106991_106992delinsTT , LRG_311:g.106991_106992delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1262_1263delinsTT ENSP00000514759.2:p.Glu421Val
ENST00000710265.1:c.*198_*199delinsTT ENSP00000518161.1:n.*198_*199delinsTT
ENST00000688158.2:n.1904_1905delinsTT
ENST00000688922.2:c.*999_*1000delinsTT ENSP00000508742.2:n.*999_*1000delinsTT
ENST00000700021.1:c.1124_1125delinsTT ENSP00000514757.1:p.Glu375Val
ENST00000700022.1:c.*508_*509delinsTT ENSP00000514758.1:n.*508_*509delinsTT
ENST00000700023.1:n.2327_2328delinsTT
ENST00000700024.1:n.2561_2562delinsTT
ENST00000706954.1:c.1169_1170delinsTT ENSP00000516674.1:p.Glu390Val
ENST00000706955.1:c.*1204_*1205delinsTT ENSP00000516675.1:n.*1204_*1205delinsTT
ENST00000686459.1:c.*755_*756delinsTT ENSP00000508909.1:n.*755_*756delinsTT
ENST00000688158.1:c.*1280_*1281delinsTT ENSP00000509254.1:n.*1280_*1281delinsTT
ENST00000688308.1:c.1169_1170delinsTT ENSP00000508752.1:p.Glu390Val
ENST00000688922.1:c.1090_1091delinsTT
ENST00000693560.1:c.1688_1689delinsTT ENSP00000509861.1:p.Glu563Val
ENST00000371953.8:c.1169_1170delinsTT MANE Select ENSP00000361021.3:p.Glu390Val
ENST00000371953.7:c.1169_1170delinsTT ENSP00000361021.3:p.Glu390Val
NM_000314.5:c.1169_1170delinsTT NP_000305.3:p.Glu390Val
NM_000314.6:c.1169_1170delinsTT NP_000305.3:p.Glu390Val
NM_001304717.2:c.1688_1689delinsTT NP_001291646.2:p.Glu563Val
NM_001304718.1:c.578_579delinsTT NP_001291647.1:p.Glu193Val
XM_006717926.2:c.1124_1125delinsTT XP_006717989.1:p.Glu375Val
XM_011539982.1:c.1073_1074delinsTT XP_011538284.1:p.Glu358Val
XR_945791.1:n.1739_1740delinsTT
NM_000314.7:c.1169_1170delinsTT NP_000305.3:p.Glu390Val
NM_001304717.5:c.1688_1689delinsTT NP_001291646.4:p.Glu563Val
NM_001304718.2:c.578_579delinsTT NP_001291647.1:p.Glu193Val
NM_000314.8:c.1169_1170delinsTT MANE Select NP_000305.3:p.Glu390Val