Canonical Allele Identifier: CA891837884
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965402_87965403delinsTT , CM000672.2:g.87965402_87965403delinsTT GRCh38
NC_000010.10:g.89725159_89725160delinsTT , CM000672.1:g.89725159_89725160delinsTT GRCh37
NC_000010.9:g.89715139_89715140delinsTT NCBI36
NG_007466.2:g.106964_106965delinsTT , LRG_311:g.106964_106965delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1235_1236delinsTT ENSP00000514759.2:p.Asp412Val
ENST00000710265.1:c.*171_*172delinsTT ENSP00000518161.1:n.*171_*172delinsTT
ENST00000688158.2:n.1877_1878delinsTT
ENST00000688922.2:c.*972_*973delinsTT ENSP00000508742.2:n.*972_*973delinsTT
ENST00000700021.1:c.1097_1098delinsTT ENSP00000514757.1:p.Asp366Val
ENST00000700022.1:c.*481_*482delinsTT ENSP00000514758.1:n.*481_*482delinsTT
ENST00000700023.1:n.2300_2301delinsTT
ENST00000700024.1:n.2534_2535delinsTT
ENST00000706954.1:c.1142_1143delinsTT ENSP00000516674.1:p.Asp381Val
ENST00000706955.1:c.*1177_*1178delinsTT ENSP00000516675.1:n.*1177_*1178delinsTT
ENST00000686459.1:c.*728_*729delinsTT ENSP00000508909.1:n.*728_*729delinsTT
ENST00000688158.1:c.*1253_*1254delinsTT ENSP00000509254.1:n.*1253_*1254delinsTT
ENST00000688308.1:c.1142_1143delinsTT ENSP00000508752.1:p.Asp381Val
ENST00000688922.1:c.1063_1064delinsTT
ENST00000693560.1:c.1661_1662delinsTT ENSP00000509861.1:p.Asp554Val
ENST00000371953.8:c.1142_1143delinsTT MANE Select ENSP00000361021.3:p.Asp381Val
ENST00000371953.7:c.1142_1143delinsTT ENSP00000361021.3:p.Asp381Val
NM_000314.5:c.1142_1143delinsTT NP_000305.3:p.Asp381Val
NM_000314.6:c.1142_1143delinsTT NP_000305.3:p.Asp381Val
NM_001304717.2:c.1661_1662delinsTT NP_001291646.2:p.Asp554Val
NM_001304718.1:c.551_552delinsTT NP_001291647.1:p.Asp184Val
XM_006717926.2:c.1097_1098delinsTT XP_006717989.1:p.Asp366Val
XM_011539982.1:c.1046_1047delinsTT XP_011538284.1:p.Asp349Val
XR_945791.1:n.1712_1713delinsTT
NM_000314.7:c.1142_1143delinsTT NP_000305.3:p.Asp381Val
NM_001304717.5:c.1661_1662delinsTT NP_001291646.4:p.Asp554Val
NM_001304718.2:c.551_552delinsTT NP_001291647.1:p.Asp184Val
NM_000314.8:c.1142_1143delinsTT MANE Select NP_000305.3:p.Asp381Val