Canonical Allele Identifier: CA1926189844

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960808A= , CM000672.2:g.87960808A=	GRCh38
NC_000010.10:g.89720565A= , CM000672.1:g.89720565A=	GRCh37
NC_000010.9:g.89710545A=	NCBI36
NG_007466.2:g.102370A= , LRG_311:g.102370A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.895-86A=	ENSP00000514759.2:n.895-86A=
ENST00000710265.1:c.802-86A=	ENSP00000518161.1:n.802-86A=
ENST00000472832.3:c.802-86A=	ENSP00000483066.2:n.802-86A=
ENST00000688158.2:n.1537-86A=
ENST00000688922.2:c.*632-86A=	ENSP00000508742.2:n.*632-86A=
ENST00000700021.1:c.757-86A=	ENSP00000514757.1:n.757-86A=
ENST00000700022.1:c.*141-86A=	ENSP00000514758.1:n.*141-86A=
ENST00000700023.1:n.1960-86A=
ENST00000700024.1:n.2194-86A=
ENST00000700025.1:n.1571-86A=
ENST00000700026.1:n.439-86A=
ENST00000700029.1:c.729-86A=
ENST00000706954.1:c.802-86A=	ENSP00000516674.1:n.802-86A=
ENST00000706955.1:c.*837-86A=	ENSP00000516675.1:n.*837-86A=
ENST00000686459.1:c.*388-86A=	ENSP00000508909.1:n.*388-86A=
ENST00000688158.1:c.*913-86A=	ENSP00000509254.1:n.*913-86A=
ENST00000688308.1:c.802-86A=	ENSP00000508752.1:n.802-86A=
ENST00000688922.1:c.723-86A=
ENST00000693560.1:c.1321-86A=	ENSP00000509861.1:n.1321-86A=
ENST00000371953.8:c.802-86A= MANE Select	ENSP00000361021.3:n.802-86A=
ENST00000371953.7:c.802-86A=	ENSP00000361021.3:n.802-86A=
ENST00000472832.2:c.229-86A=	ENSP00000483066.1:n.229-86A=
NM_000314.5:c.802-86A=	NP_000305.3:n.802-86A=
NM_000314.6:c.802-86A=	NP_000305.3:n.802-86A=
NM_001304717.2:c.1321-86A=	NP_001291646.2:n.1321-86A=
NM_001304718.1:c.211-86A=	NP_001291647.1:n.211-86A=
XM_006717926.2:c.757-86A=	XP_006717989.1:n.757-86A=
XM_011539981.1:c.802-86A=	XP_011538283.1:n.802-86A=
XM_011539982.1:c.706-86A=	XP_011538284.1:n.706-86A=
XR_945791.1:n.1372-86A=
NM_000314.7:c.802-86A=	NP_000305.3:n.802-86A=
NM_001304717.5:c.1321-86A=	NP_001291646.4:n.1321-86A=
NM_001304718.2:c.211-86A=	NP_001291647.1:n.211-86A=
NM_000314.8:c.802-86A= MANE Select	NP_000305.3:n.802-86A=