Canonical Allele Identifier: CA1926190086

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961058A= , CM000672.2:g.87961058A=	GRCh38
NC_000010.10:g.89720815A= , CM000672.1:g.89720815A=	GRCh37
NC_000010.9:g.89710795A=	NCBI36
NG_007466.2:g.102620A= , LRG_311:g.102620A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1059A=	ENSP00000514759.2:p.Lys353=
ENST00000710265.1:c.966A=	ENSP00000518161.1:p.Lys322=
ENST00000472832.3:c.966A=	ENSP00000483066.2:p.Lys322=
ENST00000688158.2:n.1701A=
ENST00000688922.2:c.*796A=	ENSP00000508742.2:n.*796A=
ENST00000700021.1:c.921A=	ENSP00000514757.1:p.Lys307=
ENST00000700022.1:c.*305A=	ENSP00000514758.1:n.*305A=
ENST00000700023.1:n.2124A=
ENST00000700024.1:n.2358A=
ENST00000700025.1:n.1735A=
ENST00000700026.1:n.603A=
ENST00000706954.1:c.966A=	ENSP00000516674.1:p.Lys322=
ENST00000706955.1:c.*1001A=	ENSP00000516675.1:n.*1001A=
ENST00000686459.1:c.*552A=	ENSP00000508909.1:n.*552A=
ENST00000688158.1:c.*1077A=	ENSP00000509254.1:n.*1077A=
ENST00000688308.1:c.966A=	ENSP00000508752.1:p.Lys322=
ENST00000688922.1:c.887A=
ENST00000693560.1:c.1485A=	ENSP00000509861.1:p.Lys495=
ENST00000371953.8:c.966A= MANE Select	ENSP00000361021.3:p.Lys322=
ENST00000371953.7:c.966A=	ENSP00000361021.3:p.Lys322=
ENST00000472832.2:c.393A=	ENSP00000483066.1:p.Lys131=
NM_000314.5:c.966A=	NP_000305.3:p.Lys322=
NM_000314.6:c.966A=	NP_000305.3:p.Lys322=
NM_001304717.2:c.1485A=	NP_001291646.2:p.Lys495=
NM_001304718.1:c.375A=	NP_001291647.1:p.Lys125=
XM_006717926.2:c.921A=	XP_006717989.1:p.Lys307=
XM_011539981.1:c.966A=	XP_011538283.1:p.Lys322=
XM_011539982.1:c.870A=	XP_011538284.1:p.Lys290=
XR_945791.1:n.1536A=
NM_000314.7:c.966A=	NP_000305.3:p.Lys322=
NM_001304717.5:c.1485A=	NP_001291646.4:p.Lys495=
NM_001304718.2:c.375A=	NP_001291647.1:p.Lys125=
NM_000314.8:c.966A= MANE Select	NP_000305.3:p.Lys322=