Canonical Allele Identifier: CA891837842
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965398_87965400delinsAGA , CM000672.2:g.87965398_87965400delinsAGA GRCh38
NC_000010.10:g.89725155_89725157delinsAGA , CM000672.1:g.89725155_89725157delinsAGA GRCh37
NC_000010.9:g.89715135_89715137delinsAGA NCBI36
NG_007466.2:g.106960_106962delinsAGA , LRG_311:g.106960_106962delinsAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1231_1233delinsAGA ENSP00000514759.2:p.Ser411Arg
ENST00000710265.1:c.*167_*169delinsAGA ENSP00000518161.1:n.*167_*169delinsAGA
ENST00000688158.2:n.1873_1875delinsAGA
ENST00000688922.2:c.*968_*970delinsAGA ENSP00000508742.2:n.*968_*970delinsAGA
ENST00000700021.1:c.1093_1095delinsAGA ENSP00000514757.1:p.Ser365Arg
ENST00000700022.1:c.*477_*479delinsAGA ENSP00000514758.1:n.*477_*479delinsAGA
ENST00000700023.1:n.2296_2298delinsAGA
ENST00000700024.1:n.2530_2532delinsAGA
ENST00000706954.1:c.1138_1140delinsAGA ENSP00000516674.1:p.Ser380Arg
ENST00000706955.1:c.*1173_*1175delinsAGA ENSP00000516675.1:n.*1173_*1175delinsAGA
ENST00000686459.1:c.*724_*726delinsAGA ENSP00000508909.1:n.*724_*726delinsAGA
ENST00000688158.1:c.*1249_*1251delinsAGA ENSP00000509254.1:n.*1249_*1251delinsAGA
ENST00000688308.1:c.1138_1140delinsAGA ENSP00000508752.1:p.Ser380Arg
ENST00000688922.1:c.1059_1061delinsAGA
ENST00000693560.1:c.1657_1659delinsAGA ENSP00000509861.1:p.Ser553Arg
ENST00000371953.8:c.1138_1140delinsAGA MANE Select ENSP00000361021.3:p.Ser380Arg
ENST00000371953.7:c.1138_1140delinsAGA ENSP00000361021.3:p.Ser380Arg
NM_000314.5:c.1138_1140delinsAGA NP_000305.3:p.Ser380Arg
NM_000314.6:c.1138_1140delinsAGA NP_000305.3:p.Ser380Arg
NM_001304717.2:c.1657_1659delinsAGA NP_001291646.2:p.Ser553Arg
NM_001304718.1:c.547_549delinsAGA NP_001291647.1:p.Ser183Arg
XM_006717926.2:c.1093_1095delinsAGA XP_006717989.1:p.Ser365Arg
XM_011539982.1:c.1042_1044delinsAGA XP_011538284.1:p.Ser348Arg
XR_945791.1:n.1708_1710delinsAGA
NM_000314.7:c.1138_1140delinsAGA NP_000305.3:p.Ser380Arg
NM_001304717.5:c.1657_1659delinsAGA NP_001291646.4:p.Ser553Arg
NM_001304718.2:c.547_549delinsAGA NP_001291647.1:p.Ser183Arg
NM_000314.8:c.1138_1140delinsAGA MANE Select NP_000305.3:p.Ser380Arg