Canonical Allele Identifier: CA891838266
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965468_87965469delinsAA , CM000672.2:g.87965468_87965469delinsAA GRCh38
NC_000010.10:g.89725225_89725226delinsAA , CM000672.1:g.89725225_89725226delinsAA GRCh37
NC_000010.9:g.89715205_89715206delinsAA NCBI36
NG_007466.2:g.107030_107031delinsAA , LRG_311:g.107030_107031delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1301_1302delinsAA ENSP00000514759.2:p.Val434Glu
ENST00000710265.1:c.*237_*238delinsAA ENSP00000518161.1:n.*237_*238delinsAA
ENST00000688158.2:n.1943_1944delinsAA
ENST00000688922.2:c.*1038_*1039delinsAA ENSP00000508742.2:n.*1038_*1039delinsAA
ENST00000700021.1:c.1163_1164delinsAA ENSP00000514757.1:p.Val388Glu
ENST00000700022.1:c.*547_*548delinsAA ENSP00000514758.1:n.*547_*548delinsAA
ENST00000700023.1:n.2366_2367delinsAA
ENST00000700024.1:n.2600_2601delinsAA
ENST00000706954.1:c.1208_1209delinsAA ENSP00000516674.1:p.Val403Glu
ENST00000706955.1:c.*1243_*1244delinsAA ENSP00000516675.1:n.*1243_*1244delinsAA
ENST00000686459.1:c.*794_*795delinsAA ENSP00000508909.1:n.*794_*795delinsAA
ENST00000688158.1:c.*1319_*1320delinsAA ENSP00000509254.1:n.*1319_*1320delinsAA
ENST00000688308.1:c.1208_1209delinsAA ENSP00000508752.1:p.Val403Glu
ENST00000688922.1:c.1129_1130delinsAA
ENST00000693560.1:c.1727_1728delinsAA ENSP00000509861.1:p.Val576Glu
ENST00000371953.8:c.1208_1209delinsAA MANE Select ENSP00000361021.3:p.Val403Glu
ENST00000371953.7:c.1208_1209delinsAA ENSP00000361021.3:p.Val403Glu
NM_000314.5:c.1208_1209delinsAA NP_000305.3:p.Val403Glu
NM_000314.6:c.1208_1209delinsAA NP_000305.3:p.Val403Glu
NM_001304717.2:c.1727_1728delinsAA NP_001291646.2:p.Val576Glu
NM_001304718.1:c.617_618delinsAA NP_001291647.1:p.Val206Glu
XM_006717926.2:c.1163_1164delinsAA XP_006717989.1:p.Val388Glu
XM_011539982.1:c.1112_1113delinsAA XP_011538284.1:p.Val371Glu
XR_945791.1:n.1778_1779delinsAA
NM_000314.7:c.1208_1209delinsAA NP_000305.3:p.Val403Glu
NM_001304717.5:c.1727_1728delinsAA NP_001291646.4:p.Val576Glu
NM_001304718.2:c.617_618delinsAA NP_001291647.1:p.Val206Glu
NM_000314.8:c.1208_1209delinsAA MANE Select NP_000305.3:p.Val403Glu