Canonical Allele Identifier: CA2579926392
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965461_87965463delinsTTG , CM000672.2:g.87965461_87965463delinsTTG GRCh38
NC_000010.10:g.89725218_89725220delinsTTG , CM000672.1:g.89725218_89725220delinsTTG GRCh37
NC_000010.9:g.89715198_89715200delinsTTG NCBI36
NG_007466.2:g.107023_107025delinsTTG , LRG_311:g.107023_107025delinsTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1294_1296delinsTTG ENSP00000514759.2:p.Thr432Leu
ENST00000710265.1:c.*230_*232delinsTTG ENSP00000518161.1:n.*230_*232delinsTTG
ENST00000688158.2:n.1936_1938delinsTTG
ENST00000688922.2:c.*1031_*1033delinsTTG ENSP00000508742.2:n.*1031_*1033delinsTTG
ENST00000700021.1:c.1156_1158delinsTTG ENSP00000514757.1:p.Thr386Leu
ENST00000700022.1:c.*540_*542delinsTTG ENSP00000514758.1:n.*540_*542delinsTTG
ENST00000700023.1:n.2359_2361delinsTTG
ENST00000700024.1:n.2593_2595delinsTTG
ENST00000706954.1:c.1201_1203delinsTTG ENSP00000516674.1:p.Thr401Leu
ENST00000706955.1:c.*1236_*1238delinsTTG ENSP00000516675.1:n.*1236_*1238delinsTTG
ENST00000686459.1:c.*787_*789delinsTTG ENSP00000508909.1:n.*787_*789delinsTTG
ENST00000688158.1:c.*1312_*1314delinsTTG ENSP00000509254.1:n.*1312_*1314delinsTTG
ENST00000688308.1:c.1201_1203delinsTTG ENSP00000508752.1:p.Thr401Leu
ENST00000688922.1:c.1122_1124delinsTTG
ENST00000693560.1:c.1720_1722delinsTTG ENSP00000509861.1:p.Thr574Leu
ENST00000371953.8:c.1201_1203delinsTTG MANE Select ENSP00000361021.3:p.Thr401Leu
ENST00000371953.7:c.1201_1203delinsTTG ENSP00000361021.3:p.Thr401Leu
NM_000314.5:c.1201_1203delinsTTG NP_000305.3:p.Thr401Leu
NM_000314.6:c.1201_1203delinsTTG NP_000305.3:p.Thr401Leu
NM_001304717.2:c.1720_1722delinsTTG NP_001291646.2:p.Thr574Leu
NM_001304718.1:c.610_612delinsTTG NP_001291647.1:p.Thr204Leu
XM_006717926.2:c.1156_1158delinsTTG XP_006717989.1:p.Thr386Leu
XM_011539982.1:c.1105_1107delinsTTG XP_011538284.1:p.Thr369Leu
XR_945791.1:n.1771_1773delinsTTG
NM_000314.7:c.1201_1203delinsTTG NP_000305.3:p.Thr401Leu
NM_001304717.5:c.1720_1722delinsTTG NP_001291646.4:p.Thr574Leu
NM_001304718.2:c.610_612delinsTTG NP_001291647.1:p.Thr204Leu
NM_000314.8:c.1201_1203delinsTTG MANE Select NP_000305.3:p.Thr401Leu