Canonical Allele Identifier: CA1926190108
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961083G= , CM000672.2:g.87961083G= GRCh38
NC_000010.10:g.89720840G= , CM000672.1:g.89720840G= GRCh37
NC_000010.9:g.89710820G= NCBI36
NG_007466.2:g.102645G= , LRG_311:g.102645G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1084G= ENSP00000514759.2:p.Asp362=
ENST00000710265.1:c.991G= ENSP00000518161.1:p.Asp331=
ENST00000472832.3:c.991G= ENSP00000483066.2:p.Asp331=
ENST00000688158.2:n.1726G=
ENST00000688922.2:c.*821G= ENSP00000508742.2:n.*821G=
ENST00000700021.1:c.946G= ENSP00000514757.1:p.Asp316=
ENST00000700022.1:c.*330G= ENSP00000514758.1:n.*330G=
ENST00000700023.1:n.2149G=
ENST00000700024.1:n.2383G=
ENST00000700025.1:n.1760G=
ENST00000700026.1:n.628G=
ENST00000706954.1:c.991G= ENSP00000516674.1:p.Asp331=
ENST00000706955.1:c.*1026G= ENSP00000516675.1:n.*1026G=
ENST00000686459.1:c.*577G= ENSP00000508909.1:n.*577G=
ENST00000688158.1:c.*1102G= ENSP00000509254.1:n.*1102G=
ENST00000688308.1:c.991G= ENSP00000508752.1:p.Asp331=
ENST00000688922.1:c.912G=
ENST00000693560.1:c.1510G= ENSP00000509861.1:p.Asp504=
ENST00000371953.8:c.991G= MANE Select ENSP00000361021.3:p.Asp331=
ENST00000371953.7:c.991G= ENSP00000361021.3:p.Asp331=
ENST00000472832.2:c.418G= ENSP00000483066.1:p.Asp140=
NM_000314.5:c.991G= NP_000305.3:p.Asp331=
NM_000314.6:c.991G= NP_000305.3:p.Asp331=
NM_001304717.2:c.1510G= NP_001291646.2:p.Asp504=
NM_001304718.1:c.400G= NP_001291647.1:p.Asp134=
XM_006717926.2:c.946G= XP_006717989.1:p.Asp316=
XM_011539981.1:c.991G= XP_011538283.1:p.Asp331=
XM_011539982.1:c.895G= XP_011538284.1:p.Asp299=
XR_945791.1:n.1561G=
NM_000314.7:c.991G= NP_000305.3:p.Asp331=
NM_001304717.5:c.1510G= NP_001291646.4:p.Asp504=
NM_001304718.2:c.400G= NP_001291647.1:p.Asp134=
NM_000314.8:c.991G= MANE Select NP_000305.3:p.Asp331=