Canonical Allele Identifier: CA1926176189

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967078C= , CM000672.2:g.87967078C=	GRCh38
NC_000010.10:g.89726835C= , CM000672.1:g.89726835C=	GRCh37
NC_000010.9:g.89716815C=	NCBI36
NG_007466.2:g.108640C= , LRG_311:g.108640C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1847C=	ENSP00000518161.1:n.*1847C=
ENST00000688158.2:n.3553C=
ENST00000706954.1:c.*1606C=	ENSP00000516674.1:n.*1606C=
ENST00000706955.1:c.*2853C=	ENSP00000516675.1:n.*2853C=
ENST00000688158.1:c.*2929C=	ENSP00000509254.1:n.*2929C=
ENST00000693560.1:c.*1606C=	ENSP00000509861.1:n.*1606C=
ENST00000371953.8:c.*1606C= MANE Select	ENSP00000361021.3:n.*1606C=
ENST00000371953.7:c.*1606C=	ENSP00000361021.3:n.*1606C=
NM_000314.5:c.*1606C=	NP_000305.3:n.*1606C=
NM_000314.6:c.*1606C=	NP_000305.3:n.*1606C=
NM_001304717.2:c.*1606C=	NP_001291646.2:n.*1606C=
NM_001304718.1:c.*1606C=	NP_001291647.1:n.*1606C=
XM_006717926.2:c.*1606C=	XP_006717989.1:n.*1606C=
XM_011539982.1:c.*1606C=	XP_011538284.1:n.*1606C=
XR_945791.1:n.3388C=
NM_000314.7:c.*1606C=	NP_000305.3:n.*1606C=
NM_001304717.5:c.*1606C=	NP_001291646.4:n.*1606C=
NM_001304718.2:c.*1606C=	NP_001291647.1:n.*1606C=
NM_000314.8:c.*1606C= MANE Select	NP_000305.3:n.*1606C=