Canonical Allele Identifier: CA1926190117

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961097A= , CM000672.2:g.87961097A=	GRCh38
NC_000010.10:g.89720854A= , CM000672.1:g.89720854A=	GRCh37
NC_000010.9:g.89710834A=	NCBI36
NG_007466.2:g.102659A= , LRG_311:g.102659A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1098A=	ENSP00000514759.2:p.Arg366=
ENST00000710265.1:c.1005A=	ENSP00000518161.1:p.Arg335=
ENST00000472832.3:c.1005A=	ENSP00000483066.2:p.Arg335=
ENST00000688158.2:n.1740A=
ENST00000688922.2:c.*835A=	ENSP00000508742.2:n.*835A=
ENST00000700021.1:c.960A=	ENSP00000514757.1:p.Arg320=
ENST00000700022.1:c.*344A=	ENSP00000514758.1:n.*344A=
ENST00000700023.1:n.2163A=
ENST00000700024.1:n.2397A=
ENST00000700025.1:n.1774A=
ENST00000700026.1:n.642A=
ENST00000706954.1:c.1005A=	ENSP00000516674.1:p.Arg335=
ENST00000706955.1:c.*1040A=	ENSP00000516675.1:n.*1040A=
ENST00000686459.1:c.*591A=	ENSP00000508909.1:n.*591A=
ENST00000688158.1:c.*1116A=	ENSP00000509254.1:n.*1116A=
ENST00000688308.1:c.1005A=	ENSP00000508752.1:p.Arg335=
ENST00000688922.1:c.926A=
ENST00000693560.1:c.1524A=	ENSP00000509861.1:p.Arg508=
ENST00000371953.8:c.1005A= MANE Select	ENSP00000361021.3:p.Arg335=
ENST00000371953.7:c.1005A=	ENSP00000361021.3:p.Arg335=
ENST00000472832.2:c.432A=	ENSP00000483066.1:p.Arg144=
NM_000314.5:c.1005A=	NP_000305.3:p.Arg335=
NM_000314.6:c.1005A=	NP_000305.3:p.Arg335=
NM_001304717.2:c.1524A=	NP_001291646.2:p.Arg508=
NM_001304718.1:c.414A=	NP_001291647.1:p.Arg138=
XM_006717926.2:c.960A=	XP_006717989.1:p.Arg320=
XM_011539981.1:c.1005A=	XP_011538283.1:p.Arg335=
XM_011539982.1:c.909A=	XP_011538284.1:p.Arg303=
XR_945791.1:n.1575A=
NM_000314.7:c.1005A=	NP_000305.3:p.Arg335=
NM_001304717.5:c.1524A=	NP_001291646.4:p.Arg508=
NM_001304718.2:c.414A=	NP_001291647.1:p.Arg138=
NM_000314.8:c.1005A= MANE Select	NP_000305.3:p.Arg335=