Canonical Allele Identifier: CA891838189
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965449_87965450delinsGT , CM000672.2:g.87965449_87965450delinsGT GRCh38
NC_000010.10:g.89725206_89725207delinsGT , CM000672.1:g.89725206_89725207delinsGT GRCh37
NC_000010.9:g.89715186_89715187delinsGT NCBI36
NG_007466.2:g.107011_107012delinsGT , LRG_311:g.107011_107012delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1282_1283delinsGT ENSP00000514759.2:p.His428Val
ENST00000710265.1:c.*218_*219delinsGT ENSP00000518161.1:n.*218_*219delinsGT
ENST00000688158.2:n.1924_1925delinsGT
ENST00000688922.2:c.*1019_*1020delinsGT ENSP00000508742.2:n.*1019_*1020delinsGT
ENST00000700021.1:c.1144_1145delinsGT ENSP00000514757.1:p.His382Val
ENST00000700022.1:c.*528_*529delinsGT ENSP00000514758.1:n.*528_*529delinsGT
ENST00000700023.1:n.2347_2348delinsGT
ENST00000700024.1:n.2581_2582delinsGT
ENST00000706954.1:c.1189_1190delinsGT ENSP00000516674.1:p.His397Val
ENST00000706955.1:c.*1224_*1225delinsGT ENSP00000516675.1:n.*1224_*1225delinsGT
ENST00000686459.1:c.*775_*776delinsGT ENSP00000508909.1:n.*775_*776delinsGT
ENST00000688158.1:c.*1300_*1301delinsGT ENSP00000509254.1:n.*1300_*1301delinsGT
ENST00000688308.1:c.1189_1190delinsGT ENSP00000508752.1:p.His397Val
ENST00000688922.1:c.1110_1111delinsGT
ENST00000693560.1:c.1708_1709delinsGT ENSP00000509861.1:p.His570Val
ENST00000371953.8:c.1189_1190delinsGT MANE Select ENSP00000361021.3:p.His397Val
ENST00000371953.7:c.1189_1190delinsGT ENSP00000361021.3:p.His397Val
NM_000314.5:c.1189_1190delinsGT NP_000305.3:p.His397Val
NM_000314.6:c.1189_1190delinsGT NP_000305.3:p.His397Val
NM_001304717.2:c.1708_1709delinsGT NP_001291646.2:p.His570Val
NM_001304718.1:c.598_599delinsGT NP_001291647.1:p.His200Val
XM_006717926.2:c.1144_1145delinsGT XP_006717989.1:p.His382Val
XM_011539982.1:c.1093_1094delinsGT XP_011538284.1:p.His365Val
XR_945791.1:n.1759_1760delinsGT
NM_000314.7:c.1189_1190delinsGT NP_000305.3:p.His397Val
NM_001304717.5:c.1708_1709delinsGT NP_001291646.4:p.His570Val
NM_001304718.2:c.598_599delinsGT NP_001291647.1:p.His200Val
NM_000314.8:c.1189_1190delinsGT MANE Select NP_000305.3:p.His397Val