Canonical Allele Identifier: CA1926174047

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965444A= , CM000672.2:g.87965444A=	GRCh38
NC_000010.10:g.89725201A= , CM000672.1:g.89725201A=	GRCh37
NC_000010.9:g.89715181A=	NCBI36
NG_007466.2:g.107006A= , LRG_311:g.107006A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1277A=	ENSP00000514759.2:p.Asp426=
ENST00000710265.1:c.*213A=	ENSP00000518161.1:n.*213A=
ENST00000688158.2:n.1919A=
ENST00000688922.2:c.*1014A=	ENSP00000508742.2:n.*1014A=
ENST00000700021.1:c.1139A=	ENSP00000514757.1:p.Asp380=
ENST00000700022.1:c.*523A=	ENSP00000514758.1:n.*523A=
ENST00000700023.1:n.2342A=
ENST00000700024.1:n.2576A=
ENST00000706954.1:c.1184A=	ENSP00000516674.1:p.Asp395=
ENST00000706955.1:c.*1219A=	ENSP00000516675.1:n.*1219A=
ENST00000686459.1:c.*770A=	ENSP00000508909.1:n.*770A=
ENST00000688158.1:c.*1295A=	ENSP00000509254.1:n.*1295A=
ENST00000688308.1:c.1184A=	ENSP00000508752.1:p.Asp395=
ENST00000688922.1:c.1105A=
ENST00000693560.1:c.1703A=	ENSP00000509861.1:p.Asp568=
ENST00000371953.8:c.1184A= MANE Select	ENSP00000361021.3:p.Asp395=
ENST00000371953.7:c.1184A=	ENSP00000361021.3:p.Asp395=
NM_000314.5:c.1184A=	NP_000305.3:p.Asp395=
NM_000314.6:c.1184A=	NP_000305.3:p.Asp395=
NM_001304717.2:c.1703A=	NP_001291646.2:p.Asp568=
NM_001304718.1:c.593A=	NP_001291647.1:p.Asp198=
XM_006717926.2:c.1139A=	XP_006717989.1:p.Asp380=
XM_011539982.1:c.1088A=	XP_011538284.1:p.Asp363=
XR_945791.1:n.1754A=
NM_000314.7:c.1184A=	NP_000305.3:p.Asp395=
NM_001304717.5:c.1703A=	NP_001291646.4:p.Asp568=
NM_001304718.2:c.593A=	NP_001291647.1:p.Asp198=
NM_000314.8:c.1184A= MANE Select	NP_000305.3:p.Asp395=