Canonical Allele Identifier: CA891837852
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965398_87965399delinsAT , CM000672.2:g.87965398_87965399delinsAT GRCh38
NC_000010.10:g.89725155_89725156delinsAT , CM000672.1:g.89725155_89725156delinsAT GRCh37
NC_000010.9:g.89715135_89715136delinsAT NCBI36
NG_007466.2:g.106960_106961delinsAT , LRG_311:g.106960_106961delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1231_1232delinsAT ENSP00000514759.2:p.Ser411Ile
ENST00000710265.1:c.*167_*168delinsAT ENSP00000518161.1:n.*167_*168delinsAT
ENST00000688158.2:n.1873_1874delinsAT
ENST00000688922.2:c.*968_*969delinsAT ENSP00000508742.2:n.*968_*969delinsAT
ENST00000700021.1:c.1093_1094delinsAT ENSP00000514757.1:p.Ser365Ile
ENST00000700022.1:c.*477_*478delinsAT ENSP00000514758.1:n.*477_*478delinsAT
ENST00000700023.1:n.2296_2297delinsAT
ENST00000700024.1:n.2530_2531delinsAT
ENST00000706954.1:c.1138_1139delinsAT ENSP00000516674.1:p.Ser380Ile
ENST00000706955.1:c.*1173_*1174delinsAT ENSP00000516675.1:n.*1173_*1174delinsAT
ENST00000686459.1:c.*724_*725delinsAT ENSP00000508909.1:n.*724_*725delinsAT
ENST00000688158.1:c.*1249_*1250delinsAT ENSP00000509254.1:n.*1249_*1250delinsAT
ENST00000688308.1:c.1138_1139delinsAT ENSP00000508752.1:p.Ser380Ile
ENST00000688922.1:c.1059_1060delinsAT
ENST00000693560.1:c.1657_1658delinsAT ENSP00000509861.1:p.Ser553Ile
ENST00000371953.8:c.1138_1139delinsAT MANE Select ENSP00000361021.3:p.Ser380Ile
ENST00000371953.7:c.1138_1139delinsAT ENSP00000361021.3:p.Ser380Ile
NM_000314.5:c.1138_1139delinsAT NP_000305.3:p.Ser380Ile
NM_000314.6:c.1138_1139delinsAT NP_000305.3:p.Ser380Ile
NM_001304717.2:c.1657_1658delinsAT NP_001291646.2:p.Ser553Ile
NM_001304718.1:c.547_548delinsAT NP_001291647.1:p.Ser183Ile
XM_006717926.2:c.1093_1094delinsAT XP_006717989.1:p.Ser365Ile
XM_011539982.1:c.1042_1043delinsAT XP_011538284.1:p.Ser348Ile
XR_945791.1:n.1708_1709delinsAT
NM_000314.7:c.1138_1139delinsAT NP_000305.3:p.Ser380Ile
NM_001304717.5:c.1657_1658delinsAT NP_001291646.4:p.Ser553Ile
NM_001304718.2:c.547_548delinsAT NP_001291647.1:p.Ser183Ile
NM_000314.8:c.1138_1139delinsAT MANE Select NP_000305.3:p.Ser380Ile