Canonical Allele Identifier: CA891839973
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957984_87957985delinsTG , CM000672.2:g.87957984_87957985delinsTG GRCh38
NC_000010.10:g.89717741_89717742delinsTG , CM000672.1:g.89717741_89717742delinsTG GRCh37
NC_000010.9:g.89707721_89707722delinsTG NCBI36
NG_007466.2:g.99546_99547delinsTG , LRG_311:g.99546_99547delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.766_767delinsTG ENSP00000514759.2:p.Glu256Trp
ENST00000710265.1:c.766_767delinsTG ENSP00000518161.1:p.Glu256Trp
ENST00000472832.3:c.766_767delinsTG ENSP00000483066.2:p.Glu256Trp
ENST00000688158.2:n.1501_1502delinsTG
ENST00000688922.2:c.*596_*597delinsTG ENSP00000508742.2:n.*596_*597delinsTG
ENST00000700021.1:c.721_722delinsTG ENSP00000514757.1:p.Glu241Trp
ENST00000700022.1:c.*105_*106delinsTG ENSP00000514758.1:n.*105_*106delinsTG
ENST00000700023.1:n.1924_1925delinsTG
ENST00000700024.1:n.2158_2159delinsTG
ENST00000700025.1:n.1535_1536delinsTG
ENST00000700026.1:n.403_404delinsTG
ENST00000700029.1:c.600_601delinsTG
ENST00000706954.1:c.766_767delinsTG ENSP00000516674.1:p.Glu256Trp
ENST00000706955.1:c.*801_*802delinsTG ENSP00000516675.1:n.*801_*802delinsTG
ENST00000686459.1:c.*352_*353delinsTG ENSP00000508909.1:n.*352_*353delinsTG
ENST00000688158.1:c.*877_*878delinsTG ENSP00000509254.1:n.*877_*878delinsTG
ENST00000688308.1:c.766_767delinsTG ENSP00000508752.1:p.Glu256Trp
ENST00000688922.1:c.687_688delinsTG
ENST00000693560.1:c.1285_1286delinsTG ENSP00000509861.1:p.Glu429Trp
ENST00000371953.8:c.766_767delinsTG MANE Select ENSP00000361021.3:p.Glu256Trp
ENST00000371953.7:c.766_767delinsTG ENSP00000361021.3:p.Glu256Trp
ENST00000472832.2:c.193_194delinsTG ENSP00000483066.1:p.Glu65Trp
NM_000314.5:c.766_767delinsTG NP_000305.3:p.Glu256Trp
NM_000314.6:c.766_767delinsTG NP_000305.3:p.Glu256Trp
NM_001304717.2:c.1285_1286delinsTG NP_001291646.2:p.Glu429Trp
NM_001304718.1:c.175_176delinsTG NP_001291647.1:p.Glu59Trp
XM_006717926.2:c.721_722delinsTG XP_006717989.1:p.Glu241Trp
XM_011539981.1:c.766_767delinsTG XP_011538283.1:p.Glu256Trp
XM_011539982.1:c.670_671delinsTG XP_011538284.1:p.Glu224Trp
XR_945791.1:n.1336_1337delinsTG
NM_000314.7:c.766_767delinsTG NP_000305.3:p.Glu256Trp
NM_001304717.5:c.1285_1286delinsTG NP_001291646.4:p.Glu429Trp
NM_001304718.2:c.175_176delinsTG NP_001291647.1:p.Glu59Trp
NM_000314.8:c.766_767delinsTG MANE Select NP_000305.3:p.Glu256Trp