Canonical Allele Identifier: CA891837876
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965401_87965403delinsTAT , CM000672.2:g.87965401_87965403delinsTAT GRCh38
NC_000010.10:g.89725158_89725160delinsTAT , CM000672.1:g.89725158_89725160delinsTAT GRCh37
NC_000010.9:g.89715138_89715140delinsTAT NCBI36
NG_007466.2:g.106963_106965delinsTAT , LRG_311:g.106963_106965delinsTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1234_1236delinsTAT ENSP00000514759.2:p.Asp412Tyr
ENST00000710265.1:c.*170_*172delinsTAT ENSP00000518161.1:n.*170_*172delinsTAT
ENST00000688158.2:n.1876_1878delinsTAT
ENST00000688922.2:c.*971_*973delinsTAT ENSP00000508742.2:n.*971_*973delinsTAT
ENST00000700021.1:c.1096_1098delinsTAT ENSP00000514757.1:p.Asp366Tyr
ENST00000700022.1:c.*480_*482delinsTAT ENSP00000514758.1:n.*480_*482delinsTAT
ENST00000700023.1:n.2299_2301delinsTAT
ENST00000700024.1:n.2533_2535delinsTAT
ENST00000706954.1:c.1141_1143delinsTAT ENSP00000516674.1:p.Asp381Tyr
ENST00000706955.1:c.*1176_*1178delinsTAT ENSP00000516675.1:n.*1176_*1178delinsTAT
ENST00000686459.1:c.*727_*729delinsTAT ENSP00000508909.1:n.*727_*729delinsTAT
ENST00000688158.1:c.*1252_*1254delinsTAT ENSP00000509254.1:n.*1252_*1254delinsTAT
ENST00000688308.1:c.1141_1143delinsTAT ENSP00000508752.1:p.Asp381Tyr
ENST00000688922.1:c.1062_1064delinsTAT
ENST00000693560.1:c.1660_1662delinsTAT ENSP00000509861.1:p.Asp554Tyr
ENST00000371953.8:c.1141_1143delinsTAT MANE Select ENSP00000361021.3:p.Asp381Tyr
ENST00000371953.7:c.1141_1143delinsTAT ENSP00000361021.3:p.Asp381Tyr
NM_000314.5:c.1141_1143delinsTAT NP_000305.3:p.Asp381Tyr
NM_000314.6:c.1141_1143delinsTAT NP_000305.3:p.Asp381Tyr
NM_001304717.2:c.1660_1662delinsTAT NP_001291646.2:p.Asp554Tyr
NM_001304718.1:c.550_552delinsTAT NP_001291647.1:p.Asp184Tyr
XM_006717926.2:c.1096_1098delinsTAT XP_006717989.1:p.Asp366Tyr
XM_011539982.1:c.1045_1047delinsTAT XP_011538284.1:p.Asp349Tyr
XR_945791.1:n.1711_1713delinsTAT
NM_000314.7:c.1141_1143delinsTAT NP_000305.3:p.Asp381Tyr
NM_001304717.5:c.1660_1662delinsTAT NP_001291646.4:p.Asp554Tyr
NM_001304718.2:c.550_552delinsTAT NP_001291647.1:p.Asp184Tyr
NM_000314.8:c.1141_1143delinsTAT MANE Select NP_000305.3:p.Asp381Tyr