Canonical Allele Identifier: CA1926190062
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961033A= , CM000672.2:g.87961033A= GRCh38
NC_000010.10:g.89720790A= , CM000672.1:g.89720790A= GRCh37
NC_000010.9:g.89710770A= NCBI36
NG_007466.2:g.102595A= , LRG_311:g.102595A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1034A= ENSP00000514759.2:p.Glu345=
ENST00000710265.1:c.941A= ENSP00000518161.1:p.Glu314=
ENST00000472832.3:c.941A= ENSP00000483066.2:p.Glu314=
ENST00000688158.2:n.1676A=
ENST00000688922.2:c.*771A= ENSP00000508742.2:n.*771A=
ENST00000700021.1:c.896A= ENSP00000514757.1:p.Glu299=
ENST00000700022.1:c.*280A= ENSP00000514758.1:n.*280A=
ENST00000700023.1:n.2099A=
ENST00000700024.1:n.2333A=
ENST00000700025.1:n.1710A=
ENST00000700026.1:n.578A=
ENST00000706954.1:c.941A= ENSP00000516674.1:p.Glu314=
ENST00000706955.1:c.*976A= ENSP00000516675.1:n.*976A=
ENST00000686459.1:c.*527A= ENSP00000508909.1:n.*527A=
ENST00000688158.1:c.*1052A= ENSP00000509254.1:n.*1052A=
ENST00000688308.1:c.941A= ENSP00000508752.1:p.Glu314=
ENST00000688922.1:c.862A=
ENST00000693560.1:c.1460A= ENSP00000509861.1:p.Glu487=
ENST00000371953.8:c.941A= MANE Select ENSP00000361021.3:p.Glu314=
ENST00000371953.7:c.941A= ENSP00000361021.3:p.Glu314=
ENST00000472832.2:c.368A= ENSP00000483066.1:p.Glu123=
NM_000314.5:c.941A= NP_000305.3:p.Glu314=
NM_000314.6:c.941A= NP_000305.3:p.Glu314=
NM_001304717.2:c.1460A= NP_001291646.2:p.Glu487=
NM_001304718.1:c.350A= NP_001291647.1:p.Glu117=
XM_006717926.2:c.896A= XP_006717989.1:p.Glu299=
XM_011539981.1:c.941A= XP_011538283.1:p.Glu314=
XM_011539982.1:c.845A= XP_011538284.1:p.Glu282=
XR_945791.1:n.1511A=
NM_000314.7:c.941A= NP_000305.3:p.Glu314=
NM_001304717.5:c.1460A= NP_001291646.4:p.Glu487=
NM_001304718.2:c.350A= NP_001291647.1:p.Glu117=
NM_000314.8:c.941A= MANE Select NP_000305.3:p.Glu314=