Canonical Allele Identifier: CA1926190025
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960993G= , CM000672.2:g.87960993G= GRCh38
NC_000010.10:g.89720750G= , CM000672.1:g.89720750G= GRCh37
NC_000010.9:g.89710730G= NCBI36
NG_007466.2:g.102555G= , LRG_311:g.102555G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.994G= ENSP00000514759.2:p.Asp332=
ENST00000710265.1:c.901G= ENSP00000518161.1:p.Asp301=
ENST00000472832.3:c.901G= ENSP00000483066.2:p.Asp301=
ENST00000688158.2:n.1636G=
ENST00000688922.2:c.*731G= ENSP00000508742.2:n.*731G=
ENST00000700021.1:c.856G= ENSP00000514757.1:p.Asp286=
ENST00000700022.1:c.*240G= ENSP00000514758.1:n.*240G=
ENST00000700023.1:n.2059G=
ENST00000700024.1:n.2293G=
ENST00000700025.1:n.1670G=
ENST00000700026.1:n.538G=
ENST00000706954.1:c.901G= ENSP00000516674.1:p.Asp301=
ENST00000706955.1:c.*936G= ENSP00000516675.1:n.*936G=
ENST00000686459.1:c.*487G= ENSP00000508909.1:n.*487G=
ENST00000688158.1:c.*1012G= ENSP00000509254.1:n.*1012G=
ENST00000688308.1:c.901G= ENSP00000508752.1:p.Asp301=
ENST00000688922.1:c.822G=
ENST00000693560.1:c.1420G= ENSP00000509861.1:p.Asp474=
ENST00000371953.8:c.901G= MANE Select ENSP00000361021.3:p.Asp301=
ENST00000371953.7:c.901G= ENSP00000361021.3:p.Asp301=
ENST00000472832.2:c.328G= ENSP00000483066.1:p.Asp110=
NM_000314.5:c.901G= NP_000305.3:p.Asp301=
NM_000314.6:c.901G= NP_000305.3:p.Asp301=
NM_001304717.2:c.1420G= NP_001291646.2:p.Asp474=
NM_001304718.1:c.310G= NP_001291647.1:p.Asp104=
XM_006717926.2:c.856G= XP_006717989.1:p.Asp286=
XM_011539981.1:c.901G= XP_011538283.1:p.Asp301=
XM_011539982.1:c.805G= XP_011538284.1:p.Asp269=
XR_945791.1:n.1471G=
NM_000314.7:c.901G= NP_000305.3:p.Asp301=
NM_001304717.5:c.1420G= NP_001291646.4:p.Asp474=
NM_001304718.2:c.310G= NP_001291647.1:p.Asp104=
NM_000314.8:c.901G= MANE Select NP_000305.3:p.Asp301=