Canonical Allele Identifier: CA1926174142

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965477T= , CM000672.2:g.87965477T=	GRCh38
NC_000010.10:g.89725234T= , CM000672.1:g.89725234T=	GRCh37
NC_000010.9:g.89715214T=	NCBI36
NG_007466.2:g.107039T= , LRG_311:g.107039T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.*5T=	ENSP00000514759.2:n.*5T=
ENST00000710265.1:c.*246T=	ENSP00000518161.1:n.*246T=
ENST00000688158.2:n.1952T=
ENST00000688922.2:c.*1047T=	ENSP00000508742.2:n.*1047T=
ENST00000700021.1:c.*5T=	ENSP00000514757.1:n.*5T=
ENST00000700022.1:c.*556T=	ENSP00000514758.1:n.*556T=
ENST00000700023.1:n.2375T=
ENST00000700024.1:n.2609T=
ENST00000706954.1:c.*5T=	ENSP00000516674.1:n.*5T=
ENST00000706955.1:c.*1252T=	ENSP00000516675.1:n.*1252T=
ENST00000686459.1:c.*803T=	ENSP00000508909.1:n.*803T=
ENST00000688158.1:c.*1328T=	ENSP00000509254.1:n.*1328T=
ENST00000688308.1:c.*5T=	ENSP00000508752.1:n.*5T=
ENST00000688922.1:c.1138T=
ENST00000693560.1:c.*5T=	ENSP00000509861.1:n.*5T=
ENST00000371953.8:c.*5T= MANE Select	ENSP00000361021.3:n.*5T=
ENST00000371953.7:c.*5T=	ENSP00000361021.3:n.*5T=
NM_000314.5:c.*5T=	NP_000305.3:n.*5T=
NM_000314.6:c.*5T=	NP_000305.3:n.*5T=
NM_001304717.2:c.*5T=	NP_001291646.2:n.*5T=
NM_001304718.1:c.*5T=	NP_001291647.1:n.*5T=
XM_006717926.2:c.*5T=	XP_006717989.1:n.*5T=
XM_011539982.1:c.*5T=	XP_011538284.1:n.*5T=
XR_945791.1:n.1787T=
NM_000314.7:c.*5T=	NP_000305.3:n.*5T=
NM_001304717.5:c.*5T=	NP_001291646.4:n.*5T=
NM_001304718.2:c.*5T=	NP_001291647.1:n.*5T=
NM_000314.8:c.*5T= MANE Select	NP_000305.3:n.*5T=