Canonical Allele Identifier: CA1926190116

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961096G= , CM000672.2:g.87961096G=	GRCh38
NC_000010.10:g.89720853G= , CM000672.1:g.89720853G=	GRCh37
NC_000010.9:g.89710833G=	NCBI36
NG_007466.2:g.102658G= , LRG_311:g.102658G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1097G=	ENSP00000514759.2:p.Arg366=
ENST00000710265.1:c.1004G=	ENSP00000518161.1:p.Arg335=
ENST00000472832.3:c.1004G=	ENSP00000483066.2:p.Arg335=
ENST00000688158.2:n.1739G=
ENST00000688922.2:c.*834G=	ENSP00000508742.2:n.*834G=
ENST00000700021.1:c.959G=	ENSP00000514757.1:p.Arg320=
ENST00000700022.1:c.*343G=	ENSP00000514758.1:n.*343G=
ENST00000700023.1:n.2162G=
ENST00000700024.1:n.2396G=
ENST00000700025.1:n.1773G=
ENST00000700026.1:n.641G=
ENST00000706954.1:c.1004G=	ENSP00000516674.1:p.Arg335=
ENST00000706955.1:c.*1039G=	ENSP00000516675.1:n.*1039G=
ENST00000686459.1:c.*590G=	ENSP00000508909.1:n.*590G=
ENST00000688158.1:c.*1115G=	ENSP00000509254.1:n.*1115G=
ENST00000688308.1:c.1004G=	ENSP00000508752.1:p.Arg335=
ENST00000688922.1:c.925G=
ENST00000693560.1:c.1523G=	ENSP00000509861.1:p.Arg508=
ENST00000371953.8:c.1004G= MANE Select	ENSP00000361021.3:p.Arg335=
ENST00000371953.7:c.1004G=	ENSP00000361021.3:p.Arg335=
ENST00000472832.2:c.431G=	ENSP00000483066.1:p.Arg144=
NM_000314.5:c.1004G=	NP_000305.3:p.Arg335=
NM_000314.6:c.1004G=	NP_000305.3:p.Arg335=
NM_001304717.2:c.1523G=	NP_001291646.2:p.Arg508=
NM_001304718.1:c.413G=	NP_001291647.1:p.Arg138=
XM_006717926.2:c.959G=	XP_006717989.1:p.Arg320=
XM_011539981.1:c.1004G=	XP_011538283.1:p.Arg335=
XM_011539982.1:c.908G=	XP_011538284.1:p.Arg303=
XR_945791.1:n.1574G=
NM_000314.7:c.1004G=	NP_000305.3:p.Arg335=
NM_001304717.5:c.1523G=	NP_001291646.4:p.Arg508=
NM_001304718.2:c.413G=	NP_001291647.1:p.Arg138=
NM_000314.8:c.1004G= MANE Select	NP_000305.3:p.Arg335=