Canonical Allele Identifier: CA1926173811

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965347A= , CM000672.2:g.87965347A=	GRCh38
NC_000010.10:g.89725104A= , CM000672.1:g.89725104A=	GRCh37
NC_000010.9:g.89715084A=	NCBI36
NG_007466.2:g.106909A= , LRG_311:g.106909A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1180A=	ENSP00000514759.2:p.Thr394=
ENST00000710265.1:c.*116A=	ENSP00000518161.1:n.*116A=
ENST00000688158.2:n.1822A=
ENST00000688922.2:c.*917A=	ENSP00000508742.2:n.*917A=
ENST00000700021.1:c.1042A=	ENSP00000514757.1:p.Thr348=
ENST00000700022.1:c.*426A=	ENSP00000514758.1:n.*426A=
ENST00000700023.1:n.2245A=
ENST00000700024.1:n.2479A=
ENST00000706954.1:c.1087A=	ENSP00000516674.1:p.Thr363=
ENST00000706955.1:c.*1122A=	ENSP00000516675.1:n.*1122A=
ENST00000686459.1:c.*673A=	ENSP00000508909.1:n.*673A=
ENST00000688158.1:c.*1198A=	ENSP00000509254.1:n.*1198A=
ENST00000688308.1:c.1087A=	ENSP00000508752.1:p.Thr363=
ENST00000688922.1:c.1008A=
ENST00000693560.1:c.1606A=	ENSP00000509861.1:p.Thr536=
ENST00000371953.8:c.1087A= MANE Select	ENSP00000361021.3:p.Thr363=
ENST00000371953.7:c.1087A=	ENSP00000361021.3:p.Thr363=
NM_000314.5:c.1087A=	NP_000305.3:p.Thr363=
NM_000314.6:c.1087A=	NP_000305.3:p.Thr363=
NM_001304717.2:c.1606A=	NP_001291646.2:p.Thr536=
NM_001304718.1:c.496A=	NP_001291647.1:p.Thr166=
XM_006717926.2:c.1042A=	XP_006717989.1:p.Thr348=
XM_011539982.1:c.991A=	XP_011538284.1:p.Thr331=
XR_945791.1:n.1657A=
NM_000314.7:c.1087A=	NP_000305.3:p.Thr363=
NM_001304717.5:c.1606A=	NP_001291646.4:p.Thr536=
NM_001304718.2:c.496A=	NP_001291647.1:p.Thr166=
NM_000314.8:c.1087A= MANE Select	NP_000305.3:p.Thr363=