Canonical Allele Identifier: CA891837850
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965398_87965399delinsAA , CM000672.2:g.87965398_87965399delinsAA GRCh38
NC_000010.10:g.89725155_89725156delinsAA , CM000672.1:g.89725155_89725156delinsAA GRCh37
NC_000010.9:g.89715135_89715136delinsAA NCBI36
NG_007466.2:g.106960_106961delinsAA , LRG_311:g.106960_106961delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1231_1232delinsAA ENSP00000514759.2:p.Ser411Asn
ENST00000710265.1:c.*167_*168delinsAA ENSP00000518161.1:n.*167_*168delinsAA
ENST00000688158.2:n.1873_1874delinsAA
ENST00000688922.2:c.*968_*969delinsAA ENSP00000508742.2:n.*968_*969delinsAA
ENST00000700021.1:c.1093_1094delinsAA ENSP00000514757.1:p.Ser365Asn
ENST00000700022.1:c.*477_*478delinsAA ENSP00000514758.1:n.*477_*478delinsAA
ENST00000700023.1:n.2296_2297delinsAA
ENST00000700024.1:n.2530_2531delinsAA
ENST00000706954.1:c.1138_1139delinsAA ENSP00000516674.1:p.Ser380Asn
ENST00000706955.1:c.*1173_*1174delinsAA ENSP00000516675.1:n.*1173_*1174delinsAA
ENST00000686459.1:c.*724_*725delinsAA ENSP00000508909.1:n.*724_*725delinsAA
ENST00000688158.1:c.*1249_*1250delinsAA ENSP00000509254.1:n.*1249_*1250delinsAA
ENST00000688308.1:c.1138_1139delinsAA ENSP00000508752.1:p.Ser380Asn
ENST00000688922.1:c.1059_1060delinsAA
ENST00000693560.1:c.1657_1658delinsAA ENSP00000509861.1:p.Ser553Asn
ENST00000371953.8:c.1138_1139delinsAA MANE Select ENSP00000361021.3:p.Ser380Asn
ENST00000371953.7:c.1138_1139delinsAA ENSP00000361021.3:p.Ser380Asn
NM_000314.5:c.1138_1139delinsAA NP_000305.3:p.Ser380Asn
NM_000314.6:c.1138_1139delinsAA NP_000305.3:p.Ser380Asn
NM_001304717.2:c.1657_1658delinsAA NP_001291646.2:p.Ser553Asn
NM_001304718.1:c.547_548delinsAA NP_001291647.1:p.Ser183Asn
XM_006717926.2:c.1093_1094delinsAA XP_006717989.1:p.Ser365Asn
XM_011539982.1:c.1042_1043delinsAA XP_011538284.1:p.Ser348Asn
XR_945791.1:n.1708_1709delinsAA
NM_000314.7:c.1138_1139delinsAA NP_000305.3:p.Ser380Asn
NM_001304717.5:c.1657_1658delinsAA NP_001291646.4:p.Ser553Asn
NM_001304718.2:c.547_548delinsAA NP_001291647.1:p.Ser183Asn
NM_000314.8:c.1138_1139delinsAA MANE Select NP_000305.3:p.Ser380Asn