Canonical Allele Identifier: CA1926173706

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965331A= , CM000672.2:g.87965331A=	GRCh38
NC_000010.10:g.89725088A= , CM000672.1:g.89725088A=	GRCh37
NC_000010.9:g.89715068A=	NCBI36
NG_007466.2:g.106893A= , LRG_311:g.106893A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1164A=	ENSP00000514759.2:p.Pro388=
ENST00000710265.1:c.*100A=	ENSP00000518161.1:n.*100A=
ENST00000688158.2:n.1806A=
ENST00000688922.2:c.*901A=	ENSP00000508742.2:n.*901A=
ENST00000700021.1:c.1026A=	ENSP00000514757.1:p.Pro342=
ENST00000700022.1:c.*410A=	ENSP00000514758.1:n.*410A=
ENST00000700023.1:n.2229A=
ENST00000700024.1:n.2463A=
ENST00000706954.1:c.1071A=	ENSP00000516674.1:p.Pro357=
ENST00000706955.1:c.*1106A=	ENSP00000516675.1:n.*1106A=
ENST00000686459.1:c.*657A=	ENSP00000508909.1:n.*657A=
ENST00000688158.1:c.*1182A=	ENSP00000509254.1:n.*1182A=
ENST00000688308.1:c.1071A=	ENSP00000508752.1:p.Pro357=
ENST00000688922.1:c.992A=
ENST00000693560.1:c.1590A=	ENSP00000509861.1:p.Pro530=
ENST00000371953.8:c.1071A= MANE Select	ENSP00000361021.3:p.Pro357=
ENST00000371953.7:c.1071A=	ENSP00000361021.3:p.Pro357=
NM_000314.5:c.1071A=	NP_000305.3:p.Pro357=
NM_000314.6:c.1071A=	NP_000305.3:p.Pro357=
NM_001304717.2:c.1590A=	NP_001291646.2:p.Pro530=
NM_001304718.1:c.480A=	NP_001291647.1:p.Pro160=
XM_006717926.2:c.1026A=	XP_006717989.1:p.Pro342=
XM_011539982.1:c.975A=	XP_011538284.1:p.Pro325=
XR_945791.1:n.1641A=
NM_000314.7:c.1071A=	NP_000305.3:p.Pro357=
NM_001304717.5:c.1590A=	NP_001291646.4:p.Pro530=
NM_001304718.2:c.480A=	NP_001291647.1:p.Pro160=
NM_000314.8:c.1071A= MANE Select	NP_000305.3:p.Pro357=