Canonical Allele Identifier: CA891837851
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965398_87965399delinsGT , CM000672.2:g.87965398_87965399delinsGT GRCh38
NC_000010.10:g.89725155_89725156delinsGT , CM000672.1:g.89725155_89725156delinsGT GRCh37
NC_000010.9:g.89715135_89715136delinsGT NCBI36
NG_007466.2:g.106960_106961delinsGT , LRG_311:g.106960_106961delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1231_1232delinsGT ENSP00000514759.2:p.Ser411Val
ENST00000710265.1:c.*167_*168delinsGT ENSP00000518161.1:n.*167_*168delinsGT
ENST00000688158.2:n.1873_1874delinsGT
ENST00000688922.2:c.*968_*969delinsGT ENSP00000508742.2:n.*968_*969delinsGT
ENST00000700021.1:c.1093_1094delinsGT ENSP00000514757.1:p.Ser365Val
ENST00000700022.1:c.*477_*478delinsGT ENSP00000514758.1:n.*477_*478delinsGT
ENST00000700023.1:n.2296_2297delinsGT
ENST00000700024.1:n.2530_2531delinsGT
ENST00000706954.1:c.1138_1139delinsGT ENSP00000516674.1:p.Ser380Val
ENST00000706955.1:c.*1173_*1174delinsGT ENSP00000516675.1:n.*1173_*1174delinsGT
ENST00000686459.1:c.*724_*725delinsGT ENSP00000508909.1:n.*724_*725delinsGT
ENST00000688158.1:c.*1249_*1250delinsGT ENSP00000509254.1:n.*1249_*1250delinsGT
ENST00000688308.1:c.1138_1139delinsGT ENSP00000508752.1:p.Ser380Val
ENST00000688922.1:c.1059_1060delinsGT
ENST00000693560.1:c.1657_1658delinsGT ENSP00000509861.1:p.Ser553Val
ENST00000371953.8:c.1138_1139delinsGT MANE Select ENSP00000361021.3:p.Ser380Val
ENST00000371953.7:c.1138_1139delinsGT ENSP00000361021.3:p.Ser380Val
NM_000314.5:c.1138_1139delinsGT NP_000305.3:p.Ser380Val
NM_000314.6:c.1138_1139delinsGT NP_000305.3:p.Ser380Val
NM_001304717.2:c.1657_1658delinsGT NP_001291646.2:p.Ser553Val
NM_001304718.1:c.547_548delinsGT NP_001291647.1:p.Ser183Val
XM_006717926.2:c.1093_1094delinsGT XP_006717989.1:p.Ser365Val
XM_011539982.1:c.1042_1043delinsGT XP_011538284.1:p.Ser348Val
XR_945791.1:n.1708_1709delinsGT
NM_000314.7:c.1138_1139delinsGT NP_000305.3:p.Ser380Val
NM_001304717.5:c.1657_1658delinsGT NP_001291646.4:p.Ser553Val
NM_001304718.2:c.547_548delinsGT NP_001291647.1:p.Ser183Val
NM_000314.8:c.1138_1139delinsGT MANE Select NP_000305.3:p.Ser380Val