Canonical Allele Identifier: CA1926174207

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965523A= , CM000672.2:g.87965523A=	GRCh38
NC_000010.10:g.89725280A= , CM000672.1:g.89725280A=	GRCh37
NC_000010.9:g.89715260A=	NCBI36
NG_007466.2:g.107085A= , LRG_311:g.107085A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.*51A=	ENSP00000514759.2:n.*51A=
ENST00000710265.1:c.*292A=	ENSP00000518161.1:n.*292A=
ENST00000688158.2:n.1998A=
ENST00000688922.2:c.*1093A=	ENSP00000508742.2:n.*1093A=
ENST00000700021.1:c.*51A=	ENSP00000514757.1:n.*51A=
ENST00000700022.1:c.*602A=	ENSP00000514758.1:n.*602A=
ENST00000700023.1:n.2421A=
ENST00000700024.1:n.2655A=
ENST00000706954.1:c.*51A=	ENSP00000516674.1:n.*51A=
ENST00000706955.1:c.*1298A=	ENSP00000516675.1:n.*1298A=
ENST00000686459.1:c.*849A=	ENSP00000508909.1:n.*849A=
ENST00000688158.1:c.*1374A=	ENSP00000509254.1:n.*1374A=
ENST00000688308.1:c.*51A=	ENSP00000508752.1:n.*51A=
ENST00000688922.1:c.1184A=
ENST00000693560.1:c.*51A=	ENSP00000509861.1:n.*51A=
ENST00000371953.8:c.*51A= MANE Select	ENSP00000361021.3:n.*51A=
ENST00000371953.7:c.*51A=	ENSP00000361021.3:n.*51A=
NM_000314.5:c.*51A=	NP_000305.3:n.*51A=
NM_000314.6:c.*51A=	NP_000305.3:n.*51A=
NM_001304717.2:c.*51A=	NP_001291646.2:n.*51A=
NM_001304718.1:c.*51A=	NP_001291647.1:n.*51A=
XM_006717926.2:c.*51A=	XP_006717989.1:n.*51A=
XM_011539982.1:c.*51A=	XP_011538284.1:n.*51A=
XR_945791.1:n.1833A=
NM_000314.7:c.*51A=	NP_000305.3:n.*51A=
NM_001304717.5:c.*51A=	NP_001291646.4:n.*51A=
NM_001304718.2:c.*51A=	NP_001291647.1:n.*51A=
NM_000314.8:c.*51A= MANE Select	NP_000305.3:n.*51A=