Canonical Allele Identifier: CA891838111
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965437_87965439delinsTTG , CM000672.2:g.87965437_87965439delinsTTG GRCh38
NC_000010.10:g.89725194_89725196delinsTTG , CM000672.1:g.89725194_89725196delinsTTG GRCh37
NC_000010.9:g.89715174_89715176delinsTTG NCBI36
NG_007466.2:g.106999_107001delinsTTG , LRG_311:g.106999_107001delinsTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1270_1272delinsTTG ENSP00000514759.2:p.Asp424Leu
ENST00000710265.1:c.*206_*208delinsTTG ENSP00000518161.1:n.*206_*208delinsTTG
ENST00000688158.2:n.1912_1914delinsTTG
ENST00000688922.2:c.*1007_*1009delinsTTG ENSP00000508742.2:n.*1007_*1009delinsTTG
ENST00000700021.1:c.1132_1134delinsTTG ENSP00000514757.1:p.Asp378Leu
ENST00000700022.1:c.*516_*518delinsTTG ENSP00000514758.1:n.*516_*518delinsTTG
ENST00000700023.1:n.2335_2337delinsTTG
ENST00000700024.1:n.2569_2571delinsTTG
ENST00000706954.1:c.1177_1179delinsTTG ENSP00000516674.1:p.Asp393Leu
ENST00000706955.1:c.*1212_*1214delinsTTG ENSP00000516675.1:n.*1212_*1214delinsTTG
ENST00000686459.1:c.*763_*765delinsTTG ENSP00000508909.1:n.*763_*765delinsTTG
ENST00000688158.1:c.*1288_*1290delinsTTG ENSP00000509254.1:n.*1288_*1290delinsTTG
ENST00000688308.1:c.1177_1179delinsTTG ENSP00000508752.1:p.Asp393Leu
ENST00000688922.1:c.1098_1100delinsTTG
ENST00000693560.1:c.1696_1698delinsTTG ENSP00000509861.1:p.Asp566Leu
ENST00000371953.8:c.1177_1179delinsTTG MANE Select ENSP00000361021.3:p.Asp393Leu
ENST00000371953.7:c.1177_1179delinsTTG ENSP00000361021.3:p.Asp393Leu
NM_000314.5:c.1177_1179delinsTTG NP_000305.3:p.Asp393Leu
NM_000314.6:c.1177_1179delinsTTG NP_000305.3:p.Asp393Leu
NM_001304717.2:c.1696_1698delinsTTG NP_001291646.2:p.Asp566Leu
NM_001304718.1:c.586_588delinsTTG NP_001291647.1:p.Asp196Leu
XM_006717926.2:c.1132_1134delinsTTG XP_006717989.1:p.Asp378Leu
XM_011539982.1:c.1081_1083delinsTTG XP_011538284.1:p.Asp361Leu
XR_945791.1:n.1747_1749delinsTTG
NM_000314.7:c.1177_1179delinsTTG NP_000305.3:p.Asp393Leu
NM_001304717.5:c.1696_1698delinsTTG NP_001291646.4:p.Asp566Leu
NM_001304718.2:c.586_588delinsTTG NP_001291647.1:p.Asp196Leu
NM_000314.8:c.1177_1179delinsTTG MANE Select NP_000305.3:p.Asp393Leu