Canonical Allele Identifier: CA1926188476

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957819G= , CM000672.2:g.87957819G=	GRCh38
NC_000010.10:g.89717576G= , CM000672.1:g.89717576G=	GRCh37
NC_000010.9:g.89707556G=	NCBI36
NG_007466.2:g.99381G= , LRG_311:g.99381G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.635-34G=	ENSP00000514759.2:n.635-34G=
ENST00000710265.1:c.635-34G=	ENSP00000518161.1:n.635-34G=
ENST00000472832.3:c.635-34G=	ENSP00000483066.2:n.635-34G=
ENST00000688158.2:n.1370-34G=
ENST00000688922.2:c.*465-34G=	ENSP00000508742.2:n.*465-34G=
ENST00000700021.1:c.590-34G=	ENSP00000514757.1:n.590-34G=
ENST00000700022.1:c.493-34G=	ENSP00000514758.1:n.493-34G=
ENST00000700023.1:n.1793-34G=
ENST00000700024.1:n.2027-34G=
ENST00000700025.1:n.1404-34G=
ENST00000700026.1:n.238G=
ENST00000700029.1:c.469-34G=
ENST00000706954.1:c.635-34G=	ENSP00000516674.1:n.635-34G=
ENST00000706955.1:c.*670-34G=	ENSP00000516675.1:n.*670-34G=
ENST00000686459.1:c.*221-34G=	ENSP00000508909.1:n.*221-34G=
ENST00000688158.1:c.*746-34G=	ENSP00000509254.1:n.*746-34G=
ENST00000688308.1:c.635-34G=	ENSP00000508752.1:n.635-34G=
ENST00000688922.1:c.556-34G=
ENST00000693560.1:c.1154-34G=	ENSP00000509861.1:n.1154-34G=
ENST00000371953.8:c.635-34G= MANE Select	ENSP00000361021.3:n.635-34G=
ENST00000371953.7:c.635-34G=	ENSP00000361021.3:n.635-34G=
ENST00000472832.2:c.62-34G=	ENSP00000483066.1:n.62-34G=
NM_000314.5:c.635-34G=	NP_000305.3:n.635-34G=
NM_000314.6:c.635-34G=	NP_000305.3:n.635-34G=
NM_001304717.2:c.1154-34G=	NP_001291646.2:n.1154-34G=
NM_001304718.1:c.44-34G=	NP_001291647.1:n.44-34G=
XM_006717926.2:c.590-34G=	XP_006717989.1:n.590-34G=
XM_011539981.1:c.635-34G=	XP_011538283.1:n.635-34G=
XM_011539982.1:c.539-34G=	XP_011538284.1:n.539-34G=
XR_945791.1:n.1205-34G=
NM_000314.7:c.635-34G=	NP_000305.3:n.635-34G=
NM_001304717.5:c.1154-34G=	NP_001291646.4:n.1154-34G=
NM_001304718.2:c.44-34G=	NP_001291647.1:n.44-34G=
NM_000314.8:c.635-34G= MANE Select	NP_000305.3:n.635-34G=