Canonical Allele Identifier: CA891838105
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965437_87965439delinsAGA , CM000672.2:g.87965437_87965439delinsAGA GRCh38
NC_000010.10:g.89725194_89725196delinsAGA , CM000672.1:g.89725194_89725196delinsAGA GRCh37
NC_000010.9:g.89715174_89715176delinsAGA NCBI36
NG_007466.2:g.106999_107001delinsAGA , LRG_311:g.106999_107001delinsAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1270_1272delinsAGA ENSP00000514759.2:p.Asp424Arg
ENST00000710265.1:c.*206_*208delinsAGA ENSP00000518161.1:n.*206_*208delinsAGA
ENST00000688158.2:n.1912_1914delinsAGA
ENST00000688922.2:c.*1007_*1009delinsAGA ENSP00000508742.2:n.*1007_*1009delinsAGA
ENST00000700021.1:c.1132_1134delinsAGA ENSP00000514757.1:p.Asp378Arg
ENST00000700022.1:c.*516_*518delinsAGA ENSP00000514758.1:n.*516_*518delinsAGA
ENST00000700023.1:n.2335_2337delinsAGA
ENST00000700024.1:n.2569_2571delinsAGA
ENST00000706954.1:c.1177_1179delinsAGA ENSP00000516674.1:p.Asp393Arg
ENST00000706955.1:c.*1212_*1214delinsAGA ENSP00000516675.1:n.*1212_*1214delinsAGA
ENST00000686459.1:c.*763_*765delinsAGA ENSP00000508909.1:n.*763_*765delinsAGA
ENST00000688158.1:c.*1288_*1290delinsAGA ENSP00000509254.1:n.*1288_*1290delinsAGA
ENST00000688308.1:c.1177_1179delinsAGA ENSP00000508752.1:p.Asp393Arg
ENST00000688922.1:c.1098_1100delinsAGA
ENST00000693560.1:c.1696_1698delinsAGA ENSP00000509861.1:p.Asp566Arg
ENST00000371953.8:c.1177_1179delinsAGA MANE Select ENSP00000361021.3:p.Asp393Arg
ENST00000371953.7:c.1177_1179delinsAGA ENSP00000361021.3:p.Asp393Arg
NM_000314.5:c.1177_1179delinsAGA NP_000305.3:p.Asp393Arg
NM_000314.6:c.1177_1179delinsAGA NP_000305.3:p.Asp393Arg
NM_001304717.2:c.1696_1698delinsAGA NP_001291646.2:p.Asp566Arg
NM_001304718.1:c.586_588delinsAGA NP_001291647.1:p.Asp196Arg
XM_006717926.2:c.1132_1134delinsAGA XP_006717989.1:p.Asp378Arg
XM_011539982.1:c.1081_1083delinsAGA XP_011538284.1:p.Asp361Arg
XR_945791.1:n.1747_1749delinsAGA
NM_000314.7:c.1177_1179delinsAGA NP_000305.3:p.Asp393Arg
NM_001304717.5:c.1696_1698delinsAGA NP_001291646.4:p.Asp566Arg
NM_001304718.2:c.586_588delinsAGA NP_001291647.1:p.Asp196Arg
NM_000314.8:c.1177_1179delinsAGA MANE Select NP_000305.3:p.Asp393Arg