Canonical Allele Identifier: CA1926190102

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961074G= , CM000672.2:g.87961074G=	GRCh38
NC_000010.10:g.89720831G= , CM000672.1:g.89720831G=	GRCh37
NC_000010.9:g.89710811G=	NCBI36
NG_007466.2:g.102636G= , LRG_311:g.102636G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1075G=	ENSP00000514759.2:p.Ala359=
ENST00000710265.1:c.982G=	ENSP00000518161.1:p.Ala328=
ENST00000472832.3:c.982G=	ENSP00000483066.2:p.Ala328=
ENST00000688158.2:n.1717G=
ENST00000688922.2:c.*812G=	ENSP00000508742.2:n.*812G=
ENST00000700021.1:c.937G=	ENSP00000514757.1:p.Ala313=
ENST00000700022.1:c.*321G=	ENSP00000514758.1:n.*321G=
ENST00000700023.1:n.2140G=
ENST00000700024.1:n.2374G=
ENST00000700025.1:n.1751G=
ENST00000700026.1:n.619G=
ENST00000706954.1:c.982G=	ENSP00000516674.1:p.Ala328=
ENST00000706955.1:c.*1017G=	ENSP00000516675.1:n.*1017G=
ENST00000686459.1:c.*568G=	ENSP00000508909.1:n.*568G=
ENST00000688158.1:c.*1093G=	ENSP00000509254.1:n.*1093G=
ENST00000688308.1:c.982G=	ENSP00000508752.1:p.Ala328=
ENST00000688922.1:c.903G=
ENST00000693560.1:c.1501G=	ENSP00000509861.1:p.Ala501=
ENST00000371953.8:c.982G= MANE Select	ENSP00000361021.3:p.Ala328=
ENST00000371953.7:c.982G=	ENSP00000361021.3:p.Ala328=
ENST00000472832.2:c.409G=	ENSP00000483066.1:p.Ala137=
NM_000314.5:c.982G=	NP_000305.3:p.Ala328=
NM_000314.6:c.982G=	NP_000305.3:p.Ala328=
NM_001304717.2:c.1501G=	NP_001291646.2:p.Ala501=
NM_001304718.1:c.391G=	NP_001291647.1:p.Ala131=
XM_006717926.2:c.937G=	XP_006717989.1:p.Ala313=
XM_011539981.1:c.982G=	XP_011538283.1:p.Ala328=
XM_011539982.1:c.886G=	XP_011538284.1:p.Ala296=
XR_945791.1:n.1552G=
NM_000314.7:c.982G=	NP_000305.3:p.Ala328=
NM_001304717.5:c.1501G=	NP_001291646.4:p.Ala501=
NM_001304718.2:c.391G=	NP_001291647.1:p.Ala131=
NM_000314.8:c.982G= MANE Select	NP_000305.3:p.Ala328=