Canonical Allele Identifier: CA1926175286

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933148G= , CM000672.2:g.87933148G=	GRCh38
NC_000010.10:g.89692905G= , CM000672.1:g.89692905G=	GRCh37
NC_000010.9:g.89682885G=	NCBI36
NG_007466.2:g.74710G= , LRG_311:g.74710G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.389G=	ENSP00000514759.2:p.Arg130=
ENST00000710265.1:c.389G=	ENSP00000518161.1:p.Arg130=
ENST00000472832.3:c.389G=	ENSP00000483066.2:p.Arg130=
ENST00000688158.2:n.1124G=
ENST00000688922.2:c.*219G=	ENSP00000508742.2:n.*219G=
ENST00000700021.1:c.344G=	ENSP00000514757.1:p.Arg115=
ENST00000700022.1:c.389G=	ENSP00000514758.1:p.Arg130=
ENST00000700029.1:c.223G=
ENST00000706954.1:c.389G=	ENSP00000516674.1:p.Arg130=
ENST00000706955.1:c.*424G=	ENSP00000516675.1:n.*424G=
ENST00000686459.1:c.389G=	ENSP00000508909.1:p.Arg130=
ENST00000688158.1:c.*500G=	ENSP00000509254.1:n.*500G=
ENST00000688308.1:c.389G=	ENSP00000508752.1:p.Arg130=
ENST00000688922.1:c.310G=
ENST00000693560.1:c.908G=	ENSP00000509861.1:p.Arg303=
ENST00000371953.8:c.389G= MANE Select	ENSP00000361021.3:p.Arg130=
ENST00000371953.7:c.389G=	ENSP00000361021.3:p.Arg130=
ENST00000498703.1:n.215G=
ENST00000610634.1:c.287G=	ENSP00000477517.1:p.Arg96=
NM_000314.5:c.389G=	NP_000305.3:p.Arg130=
NM_000314.6:c.389G=	NP_000305.3:p.Arg130=
NM_001304717.2:c.908G=	NP_001291646.2:p.Arg303=
NM_001304718.1:c.-362G=	NP_001291647.1:n.-362G=
XM_006717926.2:c.344G=	XP_006717989.1:p.Arg115=
XM_011539981.1:c.389G=	XP_011538283.1:p.Arg130=
XM_011539982.1:c.293G=	XP_011538284.1:p.Arg98=
XR_945789.1:n.1101G=
XR_945790.1:n.1101G=
XR_945791.1:n.1101G=
NM_000314.7:c.389G=	NP_000305.3:p.Arg130=
NM_001304717.5:c.908G=	NP_001291646.4:p.Arg303=
NM_001304718.2:c.-362G=	NP_001291647.1:n.-362G=
NM_000314.8:c.389G= MANE Select	NP_000305.3:p.Arg130=