Canonical Allele Identifier: CA1926173940

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965383G= , CM000672.2:g.87965383G=	GRCh38
NC_000010.10:g.89725140G= , CM000672.1:g.89725140G=	GRCh37
NC_000010.9:g.89715120G=	NCBI36
NG_007466.2:g.106945G= , LRG_311:g.106945G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1216G=	ENSP00000514759.2:p.Asp406=
ENST00000710265.1:c.*152G=	ENSP00000518161.1:n.*152G=
ENST00000688158.2:n.1858G=
ENST00000688922.2:c.*953G=	ENSP00000508742.2:n.*953G=
ENST00000700021.1:c.1078G=	ENSP00000514757.1:p.Asp360=
ENST00000700022.1:c.*462G=	ENSP00000514758.1:n.*462G=
ENST00000700023.1:n.2281G=
ENST00000700024.1:n.2515G=
ENST00000706954.1:c.1123G=	ENSP00000516674.1:p.Asp375=
ENST00000706955.1:c.*1158G=	ENSP00000516675.1:n.*1158G=
ENST00000686459.1:c.*709G=	ENSP00000508909.1:n.*709G=
ENST00000688158.1:c.*1234G=	ENSP00000509254.1:n.*1234G=
ENST00000688308.1:c.1123G=	ENSP00000508752.1:p.Asp375=
ENST00000688922.1:c.1044G=
ENST00000693560.1:c.1642G=	ENSP00000509861.1:p.Asp548=
ENST00000371953.8:c.1123G= MANE Select	ENSP00000361021.3:p.Asp375=
ENST00000371953.7:c.1123G=	ENSP00000361021.3:p.Asp375=
NM_000314.5:c.1123G=	NP_000305.3:p.Asp375=
NM_000314.6:c.1123G=	NP_000305.3:p.Asp375=
NM_001304717.2:c.1642G=	NP_001291646.2:p.Asp548=
NM_001304718.1:c.532G=	NP_001291647.1:p.Asp178=
XM_006717926.2:c.1078G=	XP_006717989.1:p.Asp360=
XM_011539982.1:c.1027G=	XP_011538284.1:p.Asp343=
XR_945791.1:n.1693G=
NM_000314.7:c.1123G=	NP_000305.3:p.Asp375=
NM_001304717.5:c.1642G=	NP_001291646.4:p.Asp548=
NM_001304718.2:c.532G=	NP_001291647.1:p.Asp178=
NM_000314.8:c.1123G= MANE Select	NP_000305.3:p.Asp375=