Canonical Allele Identifier: CA1926174103

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965464A= , CM000672.2:g.87965464A=	GRCh38
NC_000010.10:g.89725221A= , CM000672.1:g.89725221A=	GRCh37
NC_000010.9:g.89715201A=	NCBI36
NG_007466.2:g.107026A= , LRG_311:g.107026A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1297A=	ENSP00000514759.2:p.Lys433=
ENST00000710265.1:c.*233A=	ENSP00000518161.1:n.*233A=
ENST00000688158.2:n.1939A=
ENST00000688922.2:c.*1034A=	ENSP00000508742.2:n.*1034A=
ENST00000700021.1:c.1159A=	ENSP00000514757.1:p.Lys387=
ENST00000700022.1:c.*543A=	ENSP00000514758.1:n.*543A=
ENST00000700023.1:n.2362A=
ENST00000700024.1:n.2596A=
ENST00000706954.1:c.1204A=	ENSP00000516674.1:p.Lys402=
ENST00000706955.1:c.*1239A=	ENSP00000516675.1:n.*1239A=
ENST00000686459.1:c.*790A=	ENSP00000508909.1:n.*790A=
ENST00000688158.1:c.*1315A=	ENSP00000509254.1:n.*1315A=
ENST00000688308.1:c.1204A=	ENSP00000508752.1:p.Lys402=
ENST00000688922.1:c.1125A=
ENST00000693560.1:c.1723A=	ENSP00000509861.1:p.Lys575=
ENST00000371953.8:c.1204A= MANE Select	ENSP00000361021.3:p.Lys402=
ENST00000371953.7:c.1204A=	ENSP00000361021.3:p.Lys402=
NM_000314.5:c.1204A=	NP_000305.3:p.Lys402=
NM_000314.6:c.1204A=	NP_000305.3:p.Lys402=
NM_001304717.2:c.1723A=	NP_001291646.2:p.Lys575=
NM_001304718.1:c.613A=	NP_001291647.1:p.Lys205=
XM_006717926.2:c.1159A=	XP_006717989.1:p.Lys387=
XM_011539982.1:c.1108A=	XP_011538284.1:p.Lys370=
XR_945791.1:n.1774A=
NM_000314.7:c.1204A=	NP_000305.3:p.Lys402=
NM_001304717.5:c.1723A=	NP_001291646.4:p.Lys575=
NM_001304718.2:c.613A=	NP_001291647.1:p.Lys205=
NM_000314.8:c.1204A= MANE Select	NP_000305.3:p.Lys402=