Canonical Allele Identifier: CA891838044
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965426_87965427delinsTG , CM000672.2:g.87965426_87965427delinsTG GRCh38
NC_000010.10:g.89725183_89725184delinsTG , CM000672.1:g.89725183_89725184delinsTG GRCh37
NC_000010.9:g.89715163_89715164delinsTG NCBI36
NG_007466.2:g.106988_106989delinsTG , LRG_311:g.106988_106989delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1259_1260delinsTG ENSP00000514759.2:p.Asn420Met
ENST00000710265.1:c.*195_*196delinsTG ENSP00000518161.1:n.*195_*196delinsTG
ENST00000688158.2:n.1901_1902delinsTG
ENST00000688922.2:c.*996_*997delinsTG ENSP00000508742.2:n.*996_*997delinsTG
ENST00000700021.1:c.1121_1122delinsTG ENSP00000514757.1:p.Asn374Met
ENST00000700022.1:c.*505_*506delinsTG ENSP00000514758.1:n.*505_*506delinsTG
ENST00000700023.1:n.2324_2325delinsTG
ENST00000700024.1:n.2558_2559delinsTG
ENST00000706954.1:c.1166_1167delinsTG ENSP00000516674.1:p.Asn389Met
ENST00000706955.1:c.*1201_*1202delinsTG ENSP00000516675.1:n.*1201_*1202delinsTG
ENST00000686459.1:c.*752_*753delinsTG ENSP00000508909.1:n.*752_*753delinsTG
ENST00000688158.1:c.*1277_*1278delinsTG ENSP00000509254.1:n.*1277_*1278delinsTG
ENST00000688308.1:c.1166_1167delinsTG ENSP00000508752.1:p.Asn389Met
ENST00000688922.1:c.1087_1088delinsTG
ENST00000693560.1:c.1685_1686delinsTG ENSP00000509861.1:p.Asn562Met
ENST00000371953.8:c.1166_1167delinsTG MANE Select ENSP00000361021.3:p.Asn389Met
ENST00000371953.7:c.1166_1167delinsTG ENSP00000361021.3:p.Asn389Met
NM_000314.5:c.1166_1167delinsTG NP_000305.3:p.Asn389Met
NM_000314.6:c.1166_1167delinsTG NP_000305.3:p.Asn389Met
NM_001304717.2:c.1685_1686delinsTG NP_001291646.2:p.Asn562Met
NM_001304718.1:c.575_576delinsTG NP_001291647.1:p.Asn192Met
XM_006717926.2:c.1121_1122delinsTG XP_006717989.1:p.Asn374Met
XM_011539982.1:c.1070_1071delinsTG XP_011538284.1:p.Asn357Met
XR_945791.1:n.1736_1737delinsTG
NM_000314.7:c.1166_1167delinsTG NP_000305.3:p.Asn389Met
NM_001304717.5:c.1685_1686delinsTG NP_001291646.4:p.Asn562Met
NM_001304718.2:c.575_576delinsTG NP_001291647.1:p.Asn192Met
NM_000314.8:c.1166_1167delinsTG MANE Select NP_000305.3:p.Asn389Met