Canonical Allele Identifier: CA2579926409
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965401_87965403delinsTCT , CM000672.2:g.87965401_87965403delinsTCT GRCh38
NC_000010.10:g.89725158_89725160delinsTCT , CM000672.1:g.89725158_89725160delinsTCT GRCh37
NC_000010.9:g.89715138_89715140delinsTCT NCBI36
NG_007466.2:g.106963_106965delinsTCT , LRG_311:g.106963_106965delinsTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1234_1236delinsTCT ENSP00000514759.2:p.Asp412Ser
ENST00000710265.1:c.*170_*172delinsTCT ENSP00000518161.1:n.*170_*172delinsTCT
ENST00000688158.2:n.1876_1878delinsTCT
ENST00000688922.2:c.*971_*973delinsTCT ENSP00000508742.2:n.*971_*973delinsTCT
ENST00000700021.1:c.1096_1098delinsTCT ENSP00000514757.1:p.Asp366Ser
ENST00000700022.1:c.*480_*482delinsTCT ENSP00000514758.1:n.*480_*482delinsTCT
ENST00000700023.1:n.2299_2301delinsTCT
ENST00000700024.1:n.2533_2535delinsTCT
ENST00000706954.1:c.1141_1143delinsTCT ENSP00000516674.1:p.Asp381Ser
ENST00000706955.1:c.*1176_*1178delinsTCT ENSP00000516675.1:n.*1176_*1178delinsTCT
ENST00000686459.1:c.*727_*729delinsTCT ENSP00000508909.1:n.*727_*729delinsTCT
ENST00000688158.1:c.*1252_*1254delinsTCT ENSP00000509254.1:n.*1252_*1254delinsTCT
ENST00000688308.1:c.1141_1143delinsTCT ENSP00000508752.1:p.Asp381Ser
ENST00000688922.1:c.1062_1064delinsTCT
ENST00000693560.1:c.1660_1662delinsTCT ENSP00000509861.1:p.Asp554Ser
ENST00000371953.8:c.1141_1143delinsTCT MANE Select ENSP00000361021.3:p.Asp381Ser
ENST00000371953.7:c.1141_1143delinsTCT ENSP00000361021.3:p.Asp381Ser
NM_000314.5:c.1141_1143delinsTCT NP_000305.3:p.Asp381Ser
NM_000314.6:c.1141_1143delinsTCT NP_000305.3:p.Asp381Ser
NM_001304717.2:c.1660_1662delinsTCT NP_001291646.2:p.Asp554Ser
NM_001304718.1:c.550_552delinsTCT NP_001291647.1:p.Asp184Ser
XM_006717926.2:c.1096_1098delinsTCT XP_006717989.1:p.Asp366Ser
XM_011539982.1:c.1045_1047delinsTCT XP_011538284.1:p.Asp349Ser
XR_945791.1:n.1711_1713delinsTCT
NM_000314.7:c.1141_1143delinsTCT NP_000305.3:p.Asp381Ser
NM_001304717.5:c.1660_1662delinsTCT NP_001291646.4:p.Asp554Ser
NM_001304718.2:c.550_552delinsTCT NP_001291647.1:p.Asp184Ser
NM_000314.8:c.1141_1143delinsTCT MANE Select NP_000305.3:p.Asp381Ser