Canonical Allele Identifier: CA1926189983

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960945G= , CM000672.2:g.87960945G=	GRCh38
NC_000010.10:g.89720702G= , CM000672.1:g.89720702G=	GRCh37
NC_000010.9:g.89710682G=	NCBI36
NG_007466.2:g.102507G= , LRG_311:g.102507G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.946G=	ENSP00000514759.2:p.Glu316=
ENST00000710265.1:c.853G=	ENSP00000518161.1:p.Glu285=
ENST00000472832.3:c.853G=	ENSP00000483066.2:p.Glu285=
ENST00000688158.2:n.1588G=
ENST00000688922.2:c.*683G=	ENSP00000508742.2:n.*683G=
ENST00000700021.1:c.808G=	ENSP00000514757.1:p.Glu270=
ENST00000700022.1:c.*192G=	ENSP00000514758.1:n.*192G=
ENST00000700023.1:n.2011G=
ENST00000700024.1:n.2245G=
ENST00000700025.1:n.1622G=
ENST00000700026.1:n.490G=
ENST00000700029.1:c.780G=
ENST00000706954.1:c.853G=	ENSP00000516674.1:p.Glu285=
ENST00000706955.1:c.*888G=	ENSP00000516675.1:n.*888G=
ENST00000686459.1:c.*439G=	ENSP00000508909.1:n.*439G=
ENST00000688158.1:c.*964G=	ENSP00000509254.1:n.*964G=
ENST00000688308.1:c.853G=	ENSP00000508752.1:p.Glu285=
ENST00000688922.1:c.774G=
ENST00000693560.1:c.1372G=	ENSP00000509861.1:p.Glu458=
ENST00000371953.8:c.853G= MANE Select	ENSP00000361021.3:p.Glu285=
ENST00000371953.7:c.853G=	ENSP00000361021.3:p.Glu285=
ENST00000472832.2:c.280G=	ENSP00000483066.1:p.Glu94=
NM_000314.5:c.853G=	NP_000305.3:p.Glu285=
NM_000314.6:c.853G=	NP_000305.3:p.Glu285=
NM_001304717.2:c.1372G=	NP_001291646.2:p.Glu458=
NM_001304718.1:c.262G=	NP_001291647.1:p.Glu88=
XM_006717926.2:c.808G=	XP_006717989.1:p.Glu270=
XM_011539981.1:c.853G=	XP_011538283.1:p.Glu285=
XM_011539982.1:c.757G=	XP_011538284.1:p.Glu253=
XR_945791.1:n.1423G=
NM_000314.7:c.853G=	NP_000305.3:p.Glu285=
NM_001304717.5:c.1372G=	NP_001291646.4:p.Glu458=
NM_001304718.2:c.262G=	NP_001291647.1:p.Glu88=
NM_000314.8:c.853G= MANE Select	NP_000305.3:p.Glu285=