Canonical Allele Identifier: CA891837877
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965401_87965403delinsTGT , CM000672.2:g.87965401_87965403delinsTGT GRCh38
NC_000010.10:g.89725158_89725160delinsTGT , CM000672.1:g.89725158_89725160delinsTGT GRCh37
NC_000010.9:g.89715138_89715140delinsTGT NCBI36
NG_007466.2:g.106963_106965delinsTGT , LRG_311:g.106963_106965delinsTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1234_1236delinsTGT ENSP00000514759.2:p.Asp412Cys
ENST00000710265.1:c.*170_*172delinsTGT ENSP00000518161.1:n.*170_*172delinsTGT
ENST00000688158.2:n.1876_1878delinsTGT
ENST00000688922.2:c.*971_*973delinsTGT ENSP00000508742.2:n.*971_*973delinsTGT
ENST00000700021.1:c.1096_1098delinsTGT ENSP00000514757.1:p.Asp366Cys
ENST00000700022.1:c.*480_*482delinsTGT ENSP00000514758.1:n.*480_*482delinsTGT
ENST00000700023.1:n.2299_2301delinsTGT
ENST00000700024.1:n.2533_2535delinsTGT
ENST00000706954.1:c.1141_1143delinsTGT ENSP00000516674.1:p.Asp381Cys
ENST00000706955.1:c.*1176_*1178delinsTGT ENSP00000516675.1:n.*1176_*1178delinsTGT
ENST00000686459.1:c.*727_*729delinsTGT ENSP00000508909.1:n.*727_*729delinsTGT
ENST00000688158.1:c.*1252_*1254delinsTGT ENSP00000509254.1:n.*1252_*1254delinsTGT
ENST00000688308.1:c.1141_1143delinsTGT ENSP00000508752.1:p.Asp381Cys
ENST00000688922.1:c.1062_1064delinsTGT
ENST00000693560.1:c.1660_1662delinsTGT ENSP00000509861.1:p.Asp554Cys
ENST00000371953.8:c.1141_1143delinsTGT MANE Select ENSP00000361021.3:p.Asp381Cys
ENST00000371953.7:c.1141_1143delinsTGT ENSP00000361021.3:p.Asp381Cys
NM_000314.5:c.1141_1143delinsTGT NP_000305.3:p.Asp381Cys
NM_000314.6:c.1141_1143delinsTGT NP_000305.3:p.Asp381Cys
NM_001304717.2:c.1660_1662delinsTGT NP_001291646.2:p.Asp554Cys
NM_001304718.1:c.550_552delinsTGT NP_001291647.1:p.Asp184Cys
XM_006717926.2:c.1096_1098delinsTGT XP_006717989.1:p.Asp366Cys
XM_011539982.1:c.1045_1047delinsTGT XP_011538284.1:p.Asp349Cys
XR_945791.1:n.1711_1713delinsTGT
NM_000314.7:c.1141_1143delinsTGT NP_000305.3:p.Asp381Cys
NM_001304717.5:c.1660_1662delinsTGT NP_001291646.4:p.Asp554Cys
NM_001304718.2:c.550_552delinsTGT NP_001291647.1:p.Asp184Cys
NM_000314.8:c.1141_1143delinsTGT MANE Select NP_000305.3:p.Asp381Cys