Canonical Allele Identifier: CA891837438
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965350_87965351delinsAT , CM000672.2:g.87965350_87965351delinsAT GRCh38
NC_000010.10:g.89725107_89725108delinsAT , CM000672.1:g.89725107_89725108delinsAT GRCh37
NC_000010.9:g.89715087_89715088delinsAT NCBI36
NG_007466.2:g.106912_106913delinsAT , LRG_311:g.106912_106913delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1183_1184delinsAT ENSP00000514759.2:p.Ser395Ile
ENST00000710265.1:c.*119_*120delinsAT ENSP00000518161.1:n.*119_*120delinsAT
ENST00000688158.2:n.1825_1826delinsAT
ENST00000688922.2:c.*920_*921delinsAT ENSP00000508742.2:n.*920_*921delinsAT
ENST00000700021.1:c.1045_1046delinsAT ENSP00000514757.1:p.Ser349Ile
ENST00000700022.1:c.*429_*430delinsAT ENSP00000514758.1:n.*429_*430delinsAT
ENST00000700023.1:n.2248_2249delinsAT
ENST00000700024.1:n.2482_2483delinsAT
ENST00000706954.1:c.1090_1091delinsAT ENSP00000516674.1:p.Ser364Ile
ENST00000706955.1:c.*1125_*1126delinsAT ENSP00000516675.1:n.*1125_*1126delinsAT
ENST00000686459.1:c.*676_*677delinsAT ENSP00000508909.1:n.*676_*677delinsAT
ENST00000688158.1:c.*1201_*1202delinsAT ENSP00000509254.1:n.*1201_*1202delinsAT
ENST00000688308.1:c.1090_1091delinsAT ENSP00000508752.1:p.Ser364Ile
ENST00000688922.1:c.1011_1012delinsAT
ENST00000693560.1:c.1609_1610delinsAT ENSP00000509861.1:p.Ser537Ile
ENST00000371953.8:c.1090_1091delinsAT MANE Select ENSP00000361021.3:p.Ser364Ile
ENST00000371953.7:c.1090_1091delinsAT ENSP00000361021.3:p.Ser364Ile
NM_000314.5:c.1090_1091delinsAT NP_000305.3:p.Ser364Ile
NM_000314.6:c.1090_1091delinsAT NP_000305.3:p.Ser364Ile
NM_001304717.2:c.1609_1610delinsAT NP_001291646.2:p.Ser537Ile
NM_001304718.1:c.499_500delinsAT NP_001291647.1:p.Ser167Ile
XM_006717926.2:c.1045_1046delinsAT XP_006717989.1:p.Ser349Ile
XM_011539982.1:c.994_995delinsAT XP_011538284.1:p.Ser332Ile
XR_945791.1:n.1660_1661delinsAT
NM_000314.7:c.1090_1091delinsAT NP_000305.3:p.Ser364Ile
NM_001304717.5:c.1609_1610delinsAT NP_001291646.4:p.Ser537Ile
NM_001304718.2:c.499_500delinsAT NP_001291647.1:p.Ser167Ile
NM_000314.8:c.1090_1091delinsAT MANE Select NP_000305.3:p.Ser364Ile