Canonical Allele Identifier: CA1926173607

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965321C= , CM000672.2:g.87965321C=	GRCh38
NC_000010.10:g.89725078C= , CM000672.1:g.89725078C=	GRCh37
NC_000010.9:g.89715058C=	NCBI36
NG_007466.2:g.106883C= , LRG_311:g.106883C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000314.8:c.1061C= MANE Select	NP_000305.3:p.Pro354=
ENST00000371953.8:c.1061C= MANE Select	ENSP00000361021.3:p.Pro354=
NM_000314.5:c.1061C=	NP_000305.3:p.Pro354=
NM_000314.6:c.1061C=	NP_000305.3:p.Pro354=
NM_000314.7:c.1061C=	NP_000305.3:p.Pro354=
NM_001304717.2:c.1580C=	NP_001291646.2:p.Pro527=
NM_001304717.5:c.1580C=	NP_001291646.4:p.Pro527=
NM_001304718.1:c.470C=	NP_001291647.1:p.Pro157=
NM_001304718.2:c.470C=	NP_001291647.1:p.Pro157=
ENST00000371953.7:c.1061C=	ENSP00000361021.3:p.Pro354=
ENST00000686459.1:c.*647C=	ENSP00000508909.1:n.*647C=
ENST00000688158.1:c.*1172C=	ENSP00000509254.1:n.*1172C=
ENST00000688158.2:n.1796C=
ENST00000688308.1:c.1061C=	ENSP00000508752.1:p.Pro354=
ENST00000688922.1:c.982C=
ENST00000688922.2:c.*891C=	ENSP00000508742.2:n.*891C=
ENST00000693560.1:c.1580C=	ENSP00000509861.1:p.Pro527=
ENST00000700021.1:c.1016C=	ENSP00000514757.1:p.Pro339=
ENST00000700022.1:c.*400C=	ENSP00000514758.1:n.*400C=
ENST00000700023.1:n.2219C=
ENST00000700024.1:n.2453C=
ENST00000700029.2:c.1154C=	ENSP00000514759.2:p.Pro385=
ENST00000706954.1:c.1061C=	ENSP00000516674.1:p.Pro354=
ENST00000706955.1:c.*1096C=	ENSP00000516675.1:n.*1096C=
ENST00000710265.1:c.*90C=	ENSP00000518161.1:n.*90C=
XM_006717926.2:c.1016C=	XP_006717989.1:p.Pro339=
XM_011539982.1:c.965C=	XP_011538284.1:p.Pro322=
XR_945791.1:n.1631C=