Canonical Allele Identifier: CA1926173986

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965392A= , CM000672.2:g.87965392A=	GRCh38
NC_000010.10:g.89725149A= , CM000672.1:g.89725149A=	GRCh37
NC_000010.9:g.89715129A=	NCBI36
NG_007466.2:g.106954A= , LRG_311:g.106954A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1225A=	ENSP00000514759.2:p.Arg409=
ENST00000710265.1:c.*161A=	ENSP00000518161.1:n.*161A=
ENST00000688158.2:n.1867A=
ENST00000688922.2:c.*962A=	ENSP00000508742.2:n.*962A=
ENST00000700021.1:c.1087A=	ENSP00000514757.1:p.Arg363=
ENST00000700022.1:c.*471A=	ENSP00000514758.1:n.*471A=
ENST00000700023.1:n.2290A=
ENST00000700024.1:n.2524A=
ENST00000706954.1:c.1132A=	ENSP00000516674.1:p.Arg378=
ENST00000706955.1:c.*1167A=	ENSP00000516675.1:n.*1167A=
ENST00000686459.1:c.*718A=	ENSP00000508909.1:n.*718A=
ENST00000688158.1:c.*1243A=	ENSP00000509254.1:n.*1243A=
ENST00000688308.1:c.1132A=	ENSP00000508752.1:p.Arg378=
ENST00000688922.1:c.1053A=
ENST00000693560.1:c.1651A=	ENSP00000509861.1:p.Arg551=
ENST00000371953.8:c.1132A= MANE Select	ENSP00000361021.3:p.Arg378=
ENST00000371953.7:c.1132A=	ENSP00000361021.3:p.Arg378=
NM_000314.5:c.1132A=	NP_000305.3:p.Arg378=
NM_000314.6:c.1132A=	NP_000305.3:p.Arg378=
NM_001304717.2:c.1651A=	NP_001291646.2:p.Arg551=
NM_001304718.1:c.541A=	NP_001291647.1:p.Arg181=
XM_006717926.2:c.1087A=	XP_006717989.1:p.Arg363=
XM_011539982.1:c.1036A=	XP_011538284.1:p.Arg346=
XR_945791.1:n.1702A=
NM_000314.7:c.1132A=	NP_000305.3:p.Arg378=
NM_001304717.5:c.1651A=	NP_001291646.4:p.Arg551=
NM_001304718.2:c.541A=	NP_001291647.1:p.Arg181=
NM_000314.8:c.1132A= MANE Select	NP_000305.3:p.Arg378=