Canonical Allele Identifier: CA1926173829

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965349T= , CM000672.2:g.87965349T=	GRCh38
NC_000010.10:g.89725106T= , CM000672.1:g.89725106T=	GRCh37
NC_000010.9:g.89715086T=	NCBI36
NG_007466.2:g.106911T= , LRG_311:g.106911T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1182T=	ENSP00000514759.2:p.Thr394=
ENST00000710265.1:c.*118T=	ENSP00000518161.1:n.*118T=
ENST00000688158.2:n.1824T=
ENST00000688922.2:c.*919T=	ENSP00000508742.2:n.*919T=
ENST00000700021.1:c.1044T=	ENSP00000514757.1:p.Thr348=
ENST00000700022.1:c.*428T=	ENSP00000514758.1:n.*428T=
ENST00000700023.1:n.2247T=
ENST00000700024.1:n.2481T=
ENST00000706954.1:c.1089T=	ENSP00000516674.1:p.Thr363=
ENST00000706955.1:c.*1124T=	ENSP00000516675.1:n.*1124T=
ENST00000686459.1:c.*675T=	ENSP00000508909.1:n.*675T=
ENST00000688158.1:c.*1200T=	ENSP00000509254.1:n.*1200T=
ENST00000688308.1:c.1089T=	ENSP00000508752.1:p.Thr363=
ENST00000688922.1:c.1010T=
ENST00000693560.1:c.1608T=	ENSP00000509861.1:p.Thr536=
ENST00000371953.8:c.1089T= MANE Select	ENSP00000361021.3:p.Thr363=
ENST00000371953.7:c.1089T=	ENSP00000361021.3:p.Thr363=
NM_000314.5:c.1089T=	NP_000305.3:p.Thr363=
NM_000314.6:c.1089T=	NP_000305.3:p.Thr363=
NM_001304717.2:c.1608T=	NP_001291646.2:p.Thr536=
NM_001304718.1:c.498T=	NP_001291647.1:p.Thr166=
XM_006717926.2:c.1044T=	XP_006717989.1:p.Thr348=
XM_011539982.1:c.993T=	XP_011538284.1:p.Thr331=
XR_945791.1:n.1659T=
NM_000314.7:c.1089T=	NP_000305.3:p.Thr363=
NM_001304717.5:c.1608T=	NP_001291646.4:p.Thr536=
NM_001304718.2:c.498T=	NP_001291647.1:p.Thr166=
NM_000314.8:c.1089T= MANE Select	NP_000305.3:p.Thr363=