Canonical Allele Identifier: CA891841676
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965437_87965439delinsAAA , CM000672.2:g.87965437_87965439delinsAAA GRCh38
NC_000010.10:g.89725194_89725196delinsAAA , CM000672.1:g.89725194_89725196delinsAAA GRCh37
NC_000010.9:g.89715174_89715176delinsAAA NCBI36
NG_007466.2:g.106999_107001delinsAAA , LRG_311:g.106999_107001delinsAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1270_1272delinsAAA ENSP00000514759.2:p.Asp424Lys
ENST00000710265.1:c.*206_*208delinsAAA ENSP00000518161.1:n.*206_*208delinsAAA
ENST00000688158.2:n.1912_1914delinsAAA
ENST00000688922.2:c.*1007_*1009delinsAAA ENSP00000508742.2:n.*1007_*1009delinsAAA
ENST00000700021.1:c.1132_1134delinsAAA ENSP00000514757.1:p.Asp378Lys
ENST00000700022.1:c.*516_*518delinsAAA ENSP00000514758.1:n.*516_*518delinsAAA
ENST00000700023.1:n.2335_2337delinsAAA
ENST00000700024.1:n.2569_2571delinsAAA
ENST00000706954.1:c.1177_1179delinsAAA ENSP00000516674.1:p.Asp393Lys
ENST00000706955.1:c.*1212_*1214delinsAAA ENSP00000516675.1:n.*1212_*1214delinsAAA
ENST00000686459.1:c.*763_*765delinsAAA ENSP00000508909.1:n.*763_*765delinsAAA
ENST00000688158.1:c.*1288_*1290delinsAAA ENSP00000509254.1:n.*1288_*1290delinsAAA
ENST00000688308.1:c.1177_1179delinsAAA ENSP00000508752.1:p.Asp393Lys
ENST00000688922.1:c.1098_1100delinsAAA
ENST00000693560.1:c.1696_1698delinsAAA ENSP00000509861.1:p.Asp566Lys
ENST00000371953.8:c.1177_1179delinsAAA MANE Select ENSP00000361021.3:p.Asp393Lys
ENST00000371953.7:c.1177_1179delinsAAA ENSP00000361021.3:p.Asp393Lys
NM_000314.5:c.1177_1179delinsAAA NP_000305.3:p.Asp393Lys
NM_000314.6:c.1177_1179delinsAAA NP_000305.3:p.Asp393Lys
NM_001304717.2:c.1696_1698delinsAAA NP_001291646.2:p.Asp566Lys
NM_001304718.1:c.586_588delinsAAA NP_001291647.1:p.Asp196Lys
XM_006717926.2:c.1132_1134delinsAAA XP_006717989.1:p.Asp378Lys
XM_011539982.1:c.1081_1083delinsAAA XP_011538284.1:p.Asp361Lys
XR_945791.1:n.1747_1749delinsAAA
NM_000314.7:c.1177_1179delinsAAA NP_000305.3:p.Asp393Lys
NM_001304717.5:c.1696_1698delinsAAA NP_001291646.4:p.Asp566Lys
NM_001304718.2:c.586_588delinsAAA NP_001291647.1:p.Asp196Lys
NM_000314.8:c.1177_1179delinsAAA MANE Select NP_000305.3:p.Asp393Lys