Canonical Allele Identifier: CA891837154
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965320_87965321delinsAT , CM000672.2:g.87965320_87965321delinsAT GRCh38
NC_000010.10:g.89725077_89725078delinsAT , CM000672.1:g.89725077_89725078delinsAT GRCh37
NC_000010.9:g.89715057_89715058delinsAT NCBI36
NG_007466.2:g.106882_106883delinsAT , LRG_311:g.106882_106883delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1153_1154delinsAT ENSP00000514759.2:p.Pro385Met
ENST00000710265.1:c.*89_*90delinsAT ENSP00000518161.1:n.*89_*90delinsAT
ENST00000688158.2:n.1795_1796delinsAT
ENST00000688922.2:c.*890_*891delinsAT ENSP00000508742.2:n.*890_*891delinsAT
ENST00000700021.1:c.1015_1016delinsAT ENSP00000514757.1:p.Pro339Met
ENST00000700022.1:c.*399_*400delinsAT ENSP00000514758.1:n.*399_*400delinsAT
ENST00000700023.1:n.2218_2219delinsAT
ENST00000700024.1:n.2452_2453delinsAT
ENST00000706954.1:c.1060_1061delinsAT ENSP00000516674.1:p.Pro354Met
ENST00000706955.1:c.*1095_*1096delinsAT ENSP00000516675.1:n.*1095_*1096delinsAT
ENST00000686459.1:c.*646_*647delinsAT ENSP00000508909.1:n.*646_*647delinsAT
ENST00000688158.1:c.*1171_*1172delinsAT ENSP00000509254.1:n.*1171_*1172delinsAT
ENST00000688308.1:c.1060_1061delinsAT ENSP00000508752.1:p.Pro354Met
ENST00000688922.1:c.981_982delinsAT
ENST00000693560.1:c.1579_1580delinsAT ENSP00000509861.1:p.Pro527Met
ENST00000371953.8:c.1060_1061delinsAT MANE Select ENSP00000361021.3:p.Pro354Met
ENST00000371953.7:c.1060_1061delinsAT ENSP00000361021.3:p.Pro354Met
NM_000314.5:c.1060_1061delinsAT NP_000305.3:p.Pro354Met
NM_000314.6:c.1060_1061delinsAT NP_000305.3:p.Pro354Met
NM_001304717.2:c.1579_1580delinsAT NP_001291646.2:p.Pro527Met
NM_001304718.1:c.469_470delinsAT NP_001291647.1:p.Pro157Met
XM_006717926.2:c.1015_1016delinsAT XP_006717989.1:p.Pro339Met
XM_011539982.1:c.964_965delinsAT XP_011538284.1:p.Pro322Met
XR_945791.1:n.1630_1631delinsAT
NM_000314.7:c.1060_1061delinsAT NP_000305.3:p.Pro354Met
NM_001304717.5:c.1579_1580delinsAT NP_001291646.4:p.Pro527Met
NM_001304718.2:c.469_470delinsAT NP_001291647.1:p.Pro157Met
NM_000314.8:c.1060_1061delinsAT MANE Select NP_000305.3:p.Pro354Met