Canonical Allele Identifier: CA891840872
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957984_87957986delinsTTT , CM000672.2:g.87957984_87957986delinsTTT GRCh38
NC_000010.10:g.89717741_89717743delinsTTT , CM000672.1:g.89717741_89717743delinsTTT GRCh37
NC_000010.9:g.89707721_89707723delinsTTT NCBI36
NG_007466.2:g.99546_99548delinsTTT , LRG_311:g.99546_99548delinsTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.766_768delinsTTT ENSP00000514759.2:p.Glu256Phe
ENST00000710265.1:c.766_768delinsTTT ENSP00000518161.1:p.Glu256Phe
ENST00000472832.3:c.766_768delinsTTT ENSP00000483066.2:p.Glu256Phe
ENST00000688158.2:n.1501_1503delinsTTT
ENST00000688922.2:c.*596_*598delinsTTT ENSP00000508742.2:n.*596_*598delinsTTT
ENST00000700021.1:c.721_723delinsTTT ENSP00000514757.1:p.Glu241Phe
ENST00000700022.1:c.*105_*107delinsTTT ENSP00000514758.1:n.*105_*107delinsTTT
ENST00000700023.1:n.1924_1926delinsTTT
ENST00000700024.1:n.2158_2160delinsTTT
ENST00000700025.1:n.1535_1537delinsTTT
ENST00000700026.1:n.403_405delinsTTT
ENST00000700029.1:c.600_602delinsTTT
ENST00000706954.1:c.766_768delinsTTT ENSP00000516674.1:p.Glu256Phe
ENST00000706955.1:c.*801_*803delinsTTT ENSP00000516675.1:n.*801_*803delinsTTT
ENST00000686459.1:c.*352_*354delinsTTT ENSP00000508909.1:n.*352_*354delinsTTT
ENST00000688158.1:c.*877_*879delinsTTT ENSP00000509254.1:n.*877_*879delinsTTT
ENST00000688308.1:c.766_768delinsTTT ENSP00000508752.1:p.Glu256Phe
ENST00000688922.1:c.687_689delinsTTT
ENST00000693560.1:c.1285_1287delinsTTT ENSP00000509861.1:p.Glu429Phe
ENST00000371953.8:c.766_768delinsTTT MANE Select ENSP00000361021.3:p.Glu256Phe
ENST00000371953.7:c.766_768delinsTTT ENSP00000361021.3:p.Glu256Phe
ENST00000472832.2:c.193_195delinsTTT ENSP00000483066.1:p.Glu65Phe
NM_000314.5:c.766_768delinsTTT NP_000305.3:p.Glu256Phe
NM_000314.6:c.766_768delinsTTT NP_000305.3:p.Glu256Phe
NM_001304717.2:c.1285_1287delinsTTT NP_001291646.2:p.Glu429Phe
NM_001304718.1:c.175_177delinsTTT NP_001291647.1:p.Glu59Phe
XM_006717926.2:c.721_723delinsTTT XP_006717989.1:p.Glu241Phe
XM_011539981.1:c.766_768delinsTTT XP_011538283.1:p.Glu256Phe
XM_011539982.1:c.670_672delinsTTT XP_011538284.1:p.Glu224Phe
XR_945791.1:n.1336_1338delinsTTT
NM_000314.7:c.766_768delinsTTT NP_000305.3:p.Glu256Phe
NM_001304717.5:c.1285_1287delinsTTT NP_001291646.4:p.Glu429Phe
NM_001304718.2:c.175_177delinsTTT NP_001291647.1:p.Glu59Phe
NM_000314.8:c.766_768delinsTTT MANE Select NP_000305.3:p.Glu256Phe