Canonical Allele Identifier: CA891837858
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965399_87965400delinsAA , CM000672.2:g.87965399_87965400delinsAA GRCh38
NC_000010.10:g.89725156_89725157delinsAA , CM000672.1:g.89725156_89725157delinsAA GRCh37
NC_000010.9:g.89715136_89715137delinsAA NCBI36
NG_007466.2:g.106961_106962delinsAA , LRG_311:g.106961_106962delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1232_1233delinsAA ENSP00000514759.2:p.Ser411Ter
ENST00000710265.1:c.*168_*169delinsAA ENSP00000518161.1:n.*168_*169delinsAA
ENST00000688158.2:n.1874_1875delinsAA
ENST00000688922.2:c.*969_*970delinsAA ENSP00000508742.2:n.*969_*970delinsAA
ENST00000700021.1:c.1094_1095delinsAA ENSP00000514757.1:p.Ser365Ter
ENST00000700022.1:c.*478_*479delinsAA ENSP00000514758.1:n.*478_*479delinsAA
ENST00000700023.1:n.2297_2298delinsAA
ENST00000700024.1:n.2531_2532delinsAA
ENST00000706954.1:c.1139_1140delinsAA ENSP00000516674.1:p.Ser380Ter
ENST00000706955.1:c.*1174_*1175delinsAA ENSP00000516675.1:n.*1174_*1175delinsAA
ENST00000686459.1:c.*725_*726delinsAA ENSP00000508909.1:n.*725_*726delinsAA
ENST00000688158.1:c.*1250_*1251delinsAA ENSP00000509254.1:n.*1250_*1251delinsAA
ENST00000688308.1:c.1139_1140delinsAA ENSP00000508752.1:p.Ser380Ter
ENST00000688922.1:c.1060_1061delinsAA
ENST00000693560.1:c.1658_1659delinsAA ENSP00000509861.1:p.Ser553Ter
ENST00000371953.8:c.1139_1140delinsAA MANE Select ENSP00000361021.3:p.Ser380Ter
ENST00000371953.7:c.1139_1140delinsAA ENSP00000361021.3:p.Ser380Ter
NM_000314.5:c.1139_1140delinsAA NP_000305.3:p.Ser380Ter
NM_000314.6:c.1139_1140delinsAA NP_000305.3:p.Ser380Ter
NM_001304717.2:c.1658_1659delinsAA NP_001291646.2:p.Ser553Ter
NM_001304718.1:c.548_549delinsAA NP_001291647.1:p.Ser183Ter
XM_006717926.2:c.1094_1095delinsAA XP_006717989.1:p.Ser365Ter
XM_011539982.1:c.1043_1044delinsAA XP_011538284.1:p.Ser348Ter
XR_945791.1:n.1709_1710delinsAA
NM_000314.7:c.1139_1140delinsAA NP_000305.3:p.Ser380Ter
NM_001304717.5:c.1658_1659delinsAA NP_001291646.4:p.Ser553Ter
NM_001304718.2:c.548_549delinsAA NP_001291647.1:p.Ser183Ter
NM_000314.8:c.1139_1140delinsAA MANE Select NP_000305.3:p.Ser380Ter