Canonical Allele Identifier: CA1926189931

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960890T= , CM000672.2:g.87960890T=	GRCh38
NC_000010.10:g.89720647T= , CM000672.1:g.89720647T=	GRCh37
NC_000010.9:g.89710627T=	NCBI36
NG_007466.2:g.102452T= , LRG_311:g.102452T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.895-4T=	ENSP00000514759.2:n.895-4T=
ENST00000710265.1:c.802-4T=	ENSP00000518161.1:n.802-4T=
ENST00000472832.3:c.802-4T=	ENSP00000483066.2:n.802-4T=
ENST00000688158.2:n.1537-4T=
ENST00000688922.2:c.*632-4T=	ENSP00000508742.2:n.*632-4T=
ENST00000700021.1:c.757-4T=	ENSP00000514757.1:n.757-4T=
ENST00000700022.1:c.*141-4T=	ENSP00000514758.1:n.*141-4T=
ENST00000700023.1:n.1960-4T=
ENST00000700024.1:n.2194-4T=
ENST00000700025.1:n.1571-4T=
ENST00000700026.1:n.439-4T=
ENST00000700029.1:c.729-4T=
ENST00000706954.1:c.802-4T=	ENSP00000516674.1:n.802-4T=
ENST00000706955.1:c.*837-4T=	ENSP00000516675.1:n.*837-4T=
ENST00000686459.1:c.*388-4T=	ENSP00000508909.1:n.*388-4T=
ENST00000688158.1:c.*913-4T=	ENSP00000509254.1:n.*913-4T=
ENST00000688308.1:c.802-4T=	ENSP00000508752.1:n.802-4T=
ENST00000688922.1:c.723-4T=
ENST00000693560.1:c.1321-4T=	ENSP00000509861.1:n.1321-4T=
ENST00000371953.8:c.802-4T= MANE Select	ENSP00000361021.3:n.802-4T=
ENST00000371953.7:c.802-4T=	ENSP00000361021.3:n.802-4T=
ENST00000472832.2:c.229-4T=	ENSP00000483066.1:n.229-4T=
NM_000314.5:c.802-4T=	NP_000305.3:n.802-4T=
NM_000314.6:c.802-4T=	NP_000305.3:n.802-4T=
NM_001304717.2:c.1321-4T=	NP_001291646.2:n.1321-4T=
NM_001304718.1:c.211-4T=	NP_001291647.1:n.211-4T=
XM_006717926.2:c.757-4T=	XP_006717989.1:n.757-4T=
XM_011539981.1:c.802-4T=	XP_011538283.1:n.802-4T=
XM_011539982.1:c.706-4T=	XP_011538284.1:n.706-4T=
XR_945791.1:n.1372-4T=
NM_000314.7:c.802-4T=	NP_000305.3:n.802-4T=
NM_001304717.5:c.1321-4T=	NP_001291646.4:n.1321-4T=
NM_001304718.2:c.211-4T=	NP_001291647.1:n.211-4T=
NM_000314.8:c.802-4T= MANE Select	NP_000305.3:n.802-4T=