Canonical Allele Identifier: CA1926173283

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965287G= , CM000672.2:g.87965287G=	GRCh38
NC_000010.10:g.89725044G= , CM000672.1:g.89725044G=	GRCh37
NC_000010.9:g.89715024G=	NCBI36
NG_007466.2:g.106849G= , LRG_311:g.106849G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1120G=	ENSP00000514759.2:p.Val374=
ENST00000710265.1:c.*56G=	ENSP00000518161.1:n.*56G=
ENST00000688158.2:n.1762G=
ENST00000688922.2:c.*857G=	ENSP00000508742.2:n.*857G=
ENST00000700021.1:c.982G=	ENSP00000514757.1:p.Val328=
ENST00000700022.1:c.*366G=	ENSP00000514758.1:n.*366G=
ENST00000700023.1:n.2185G=
ENST00000700024.1:n.2419G=
ENST00000706954.1:c.1027G=	ENSP00000516674.1:p.Val343=
ENST00000706955.1:c.*1062G=	ENSP00000516675.1:n.*1062G=
ENST00000686459.1:c.*613G=	ENSP00000508909.1:n.*613G=
ENST00000688158.1:c.*1138G=	ENSP00000509254.1:n.*1138G=
ENST00000688308.1:c.1027G=	ENSP00000508752.1:p.Val343=
ENST00000688922.1:c.948G=
ENST00000693560.1:c.1546G=	ENSP00000509861.1:p.Val516=
ENST00000371953.8:c.1027G= MANE Select	ENSP00000361021.3:p.Val343=
ENST00000371953.7:c.1027G=	ENSP00000361021.3:p.Val343=
NM_000314.5:c.1027G=	NP_000305.3:p.Val343=
NM_000314.6:c.1027G=	NP_000305.3:p.Val343=
NM_001304717.2:c.1546G=	NP_001291646.2:p.Val516=
NM_001304718.1:c.436G=	NP_001291647.1:p.Val146=
XM_006717926.2:c.982G=	XP_006717989.1:p.Val328=
XM_011539982.1:c.931G=	XP_011538284.1:p.Val311=
XR_945791.1:n.1597G=
NM_000314.7:c.1027G=	NP_000305.3:p.Val343=
NM_001304717.5:c.1546G=	NP_001291646.4:p.Val516=
NM_001304718.2:c.436G=	NP_001291647.1:p.Val146=
NM_000314.8:c.1027G= MANE Select	NP_000305.3:p.Val343=