Canonical Allele Identifier: CA1926190043

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961012A= , CM000672.2:g.87961012A=	GRCh38
NC_000010.10:g.89720769A= , CM000672.1:g.89720769A=	GRCh37
NC_000010.9:g.89710749A=	NCBI36
NG_007466.2:g.102574A= , LRG_311:g.102574A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1013A=	ENSP00000514759.2:p.Glu338=
ENST00000710265.1:c.920A=	ENSP00000518161.1:p.Glu307=
ENST00000472832.3:c.920A=	ENSP00000483066.2:p.Glu307=
ENST00000688158.2:n.1655A=
ENST00000688922.2:c.*750A=	ENSP00000508742.2:n.*750A=
ENST00000700021.1:c.875A=	ENSP00000514757.1:p.Glu292=
ENST00000700022.1:c.*259A=	ENSP00000514758.1:n.*259A=
ENST00000700023.1:n.2078A=
ENST00000700024.1:n.2312A=
ENST00000700025.1:n.1689A=
ENST00000700026.1:n.557A=
ENST00000706954.1:c.920A=	ENSP00000516674.1:p.Glu307=
ENST00000706955.1:c.*955A=	ENSP00000516675.1:n.*955A=
ENST00000686459.1:c.*506A=	ENSP00000508909.1:n.*506A=
ENST00000688158.1:c.*1031A=	ENSP00000509254.1:n.*1031A=
ENST00000688308.1:c.920A=	ENSP00000508752.1:p.Glu307=
ENST00000688922.1:c.841A=
ENST00000693560.1:c.1439A=	ENSP00000509861.1:p.Glu480=
ENST00000371953.8:c.920A= MANE Select	ENSP00000361021.3:p.Glu307=
ENST00000371953.7:c.920A=	ENSP00000361021.3:p.Glu307=
ENST00000472832.2:c.347A=	ENSP00000483066.1:p.Glu116=
NM_000314.5:c.920A=	NP_000305.3:p.Glu307=
NM_000314.6:c.920A=	NP_000305.3:p.Glu307=
NM_001304717.2:c.1439A=	NP_001291646.2:p.Glu480=
NM_001304718.1:c.329A=	NP_001291647.1:p.Glu110=
XM_006717926.2:c.875A=	XP_006717989.1:p.Glu292=
XM_011539981.1:c.920A=	XP_011538283.1:p.Glu307=
XM_011539982.1:c.824A=	XP_011538284.1:p.Glu275=
XR_945791.1:n.1490A=
NM_000314.7:c.920A=	NP_000305.3:p.Glu307=
NM_001304717.5:c.1439A=	NP_001291646.4:p.Glu480=
NM_001304718.2:c.329A=	NP_001291647.1:p.Glu110=
NM_000314.8:c.920A= MANE Select	NP_000305.3:p.Glu307=