Canonical Allele Identifier: CA1926174017

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965430A= , CM000672.2:g.87965430A=	GRCh38
NC_000010.10:g.89725187A= , CM000672.1:g.89725187A=	GRCh37
NC_000010.9:g.89715167A=	NCBI36
NG_007466.2:g.106992A= , LRG_311:g.106992A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1263A=	ENSP00000514759.2:p.Glu421=
ENST00000710265.1:c.*199A=	ENSP00000518161.1:n.*199A=
ENST00000688158.2:n.1905A=
ENST00000688922.2:c.*1000A=	ENSP00000508742.2:n.*1000A=
ENST00000700021.1:c.1125A=	ENSP00000514757.1:p.Glu375=
ENST00000700022.1:c.*509A=	ENSP00000514758.1:n.*509A=
ENST00000700023.1:n.2328A=
ENST00000700024.1:n.2562A=
ENST00000706954.1:c.1170A=	ENSP00000516674.1:p.Glu390=
ENST00000706955.1:c.*1205A=	ENSP00000516675.1:n.*1205A=
ENST00000686459.1:c.*756A=	ENSP00000508909.1:n.*756A=
ENST00000688158.1:c.*1281A=	ENSP00000509254.1:n.*1281A=
ENST00000688308.1:c.1170A=	ENSP00000508752.1:p.Glu390=
ENST00000688922.1:c.1091A=
ENST00000693560.1:c.1689A=	ENSP00000509861.1:p.Glu563=
ENST00000371953.8:c.1170A= MANE Select	ENSP00000361021.3:p.Glu390=
ENST00000371953.7:c.1170A=	ENSP00000361021.3:p.Glu390=
NM_000314.5:c.1170A=	NP_000305.3:p.Glu390=
NM_000314.6:c.1170A=	NP_000305.3:p.Glu390=
NM_001304717.2:c.1689A=	NP_001291646.2:p.Glu563=
NM_001304718.1:c.579A=	NP_001291647.1:p.Glu193=
XM_006717926.2:c.1125A=	XP_006717989.1:p.Glu375=
XM_011539982.1:c.1074A=	XP_011538284.1:p.Glu358=
XR_945791.1:n.1740A=
NM_000314.7:c.1170A=	NP_000305.3:p.Glu390=
NM_001304717.5:c.1689A=	NP_001291646.4:p.Glu563=
NM_001304718.2:c.579A=	NP_001291647.1:p.Glu193=
NM_000314.8:c.1170A= MANE Select	NP_000305.3:p.Glu390=