Canonical Allele Identifier: CA891837885
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965402_87965403delinsCT , CM000672.2:g.87965402_87965403delinsCT GRCh38
NC_000010.10:g.89725159_89725160delinsCT , CM000672.1:g.89725159_89725160delinsCT GRCh37
NC_000010.9:g.89715139_89715140delinsCT NCBI36
NG_007466.2:g.106964_106965delinsCT , LRG_311:g.106964_106965delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1235_1236delinsCT ENSP00000514759.2:p.Asp412Ala
ENST00000710265.1:c.*171_*172delinsCT ENSP00000518161.1:n.*171_*172delinsCT
ENST00000688158.2:n.1877_1878delinsCT
ENST00000688922.2:c.*972_*973delinsCT ENSP00000508742.2:n.*972_*973delinsCT
ENST00000700021.1:c.1097_1098delinsCT ENSP00000514757.1:p.Asp366Ala
ENST00000700022.1:c.*481_*482delinsCT ENSP00000514758.1:n.*481_*482delinsCT
ENST00000700023.1:n.2300_2301delinsCT
ENST00000700024.1:n.2534_2535delinsCT
ENST00000706954.1:c.1142_1143delinsCT ENSP00000516674.1:p.Asp381Ala
ENST00000706955.1:c.*1177_*1178delinsCT ENSP00000516675.1:n.*1177_*1178delinsCT
ENST00000686459.1:c.*728_*729delinsCT ENSP00000508909.1:n.*728_*729delinsCT
ENST00000688158.1:c.*1253_*1254delinsCT ENSP00000509254.1:n.*1253_*1254delinsCT
ENST00000688308.1:c.1142_1143delinsCT ENSP00000508752.1:p.Asp381Ala
ENST00000688922.1:c.1063_1064delinsCT
ENST00000693560.1:c.1661_1662delinsCT ENSP00000509861.1:p.Asp554Ala
ENST00000371953.8:c.1142_1143delinsCT MANE Select ENSP00000361021.3:p.Asp381Ala
ENST00000371953.7:c.1142_1143delinsCT ENSP00000361021.3:p.Asp381Ala
NM_000314.5:c.1142_1143delinsCT NP_000305.3:p.Asp381Ala
NM_000314.6:c.1142_1143delinsCT NP_000305.3:p.Asp381Ala
NM_001304717.2:c.1661_1662delinsCT NP_001291646.2:p.Asp554Ala
NM_001304718.1:c.551_552delinsCT NP_001291647.1:p.Asp184Ala
XM_006717926.2:c.1097_1098delinsCT XP_006717989.1:p.Asp366Ala
XM_011539982.1:c.1046_1047delinsCT XP_011538284.1:p.Asp349Ala
XR_945791.1:n.1712_1713delinsCT
NM_000314.7:c.1142_1143delinsCT NP_000305.3:p.Asp381Ala
NM_001304717.5:c.1661_1662delinsCT NP_001291646.4:p.Asp554Ala
NM_001304718.2:c.551_552delinsCT NP_001291647.1:p.Asp184Ala
NM_000314.8:c.1142_1143delinsCT MANE Select NP_000305.3:p.Asp381Ala