Canonical Allele Identifier: CA891841607
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965366_87965367delinsAA , CM000672.2:g.87965366_87965367delinsAA GRCh38
NC_000010.10:g.89725123_89725124delinsAA , CM000672.1:g.89725123_89725124delinsAA GRCh37
NC_000010.9:g.89715103_89715104delinsAA NCBI36
NG_007466.2:g.106928_106929delinsAA , LRG_311:g.106928_106929delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1199_1200delinsAA ENSP00000514759.2:p.Val400Glu
ENST00000710265.1:c.*135_*136delinsAA ENSP00000518161.1:n.*135_*136delinsAA
ENST00000688158.2:n.1841_1842delinsAA
ENST00000688922.2:c.*936_*937delinsAA ENSP00000508742.2:n.*936_*937delinsAA
ENST00000700021.1:c.1061_1062delinsAA ENSP00000514757.1:p.Val354Glu
ENST00000700022.1:c.*445_*446delinsAA ENSP00000514758.1:n.*445_*446delinsAA
ENST00000700023.1:n.2264_2265delinsAA
ENST00000700024.1:n.2498_2499delinsAA
ENST00000706954.1:c.1106_1107delinsAA ENSP00000516674.1:p.Val369Glu
ENST00000706955.1:c.*1141_*1142delinsAA ENSP00000516675.1:n.*1141_*1142delinsAA
ENST00000686459.1:c.*692_*693delinsAA ENSP00000508909.1:n.*692_*693delinsAA
ENST00000688158.1:c.*1217_*1218delinsAA ENSP00000509254.1:n.*1217_*1218delinsAA
ENST00000688308.1:c.1106_1107delinsAA ENSP00000508752.1:p.Val369Glu
ENST00000688922.1:c.1027_1028delinsAA
ENST00000693560.1:c.1625_1626delinsAA ENSP00000509861.1:p.Val542Glu
ENST00000371953.8:c.1106_1107delinsAA MANE Select ENSP00000361021.3:p.Val369Glu
ENST00000371953.7:c.1106_1107delinsAA ENSP00000361021.3:p.Val369Glu
NM_000314.5:c.1106_1107delinsAA NP_000305.3:p.Val369Glu
NM_000314.6:c.1106_1107delinsAA NP_000305.3:p.Val369Glu
NM_001304717.2:c.1625_1626delinsAA NP_001291646.2:p.Val542Glu
NM_001304718.1:c.515_516delinsAA NP_001291647.1:p.Val172Glu
XM_006717926.2:c.1061_1062delinsAA XP_006717989.1:p.Val354Glu
XM_011539982.1:c.1010_1011delinsAA XP_011538284.1:p.Val337Glu
XR_945791.1:n.1676_1677delinsAA
NM_000314.7:c.1106_1107delinsAA NP_000305.3:p.Val369Glu
NM_001304717.5:c.1625_1626delinsAA NP_001291646.4:p.Val542Glu
NM_001304718.2:c.515_516delinsAA NP_001291647.1:p.Val172Glu
NM_000314.8:c.1106_1107delinsAA MANE Select NP_000305.3:p.Val369Glu