Canonical Allele Identifier: CA1926173896

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965363A= , CM000672.2:g.87965363A=	GRCh38
NC_000010.10:g.89725120A= , CM000672.1:g.89725120A=	GRCh37
NC_000010.9:g.89715100A=	NCBI36
NG_007466.2:g.106925A= , LRG_311:g.106925A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1196A=	ENSP00000514759.2:p.Asp399=
ENST00000710265.1:c.*132A=	ENSP00000518161.1:n.*132A=
ENST00000688158.2:n.1838A=
ENST00000688922.2:c.*933A=	ENSP00000508742.2:n.*933A=
ENST00000700021.1:c.1058A=	ENSP00000514757.1:p.Asp353=
ENST00000700022.1:c.*442A=	ENSP00000514758.1:n.*442A=
ENST00000700023.1:n.2261A=
ENST00000700024.1:n.2495A=
ENST00000706954.1:c.1103A=	ENSP00000516674.1:p.Asp368=
ENST00000706955.1:c.*1138A=	ENSP00000516675.1:n.*1138A=
ENST00000686459.1:c.*689A=	ENSP00000508909.1:n.*689A=
ENST00000688158.1:c.*1214A=	ENSP00000509254.1:n.*1214A=
ENST00000688308.1:c.1103A=	ENSP00000508752.1:p.Asp368=
ENST00000688922.1:c.1024A=
ENST00000693560.1:c.1622A=	ENSP00000509861.1:p.Asp541=
ENST00000371953.8:c.1103A= MANE Select	ENSP00000361021.3:p.Asp368=
ENST00000371953.7:c.1103A=	ENSP00000361021.3:p.Asp368=
NM_000314.5:c.1103A=	NP_000305.3:p.Asp368=
NM_000314.6:c.1103A=	NP_000305.3:p.Asp368=
NM_001304717.2:c.1622A=	NP_001291646.2:p.Asp541=
NM_001304718.1:c.512A=	NP_001291647.1:p.Asp171=
XM_006717926.2:c.1058A=	XP_006717989.1:p.Asp353=
XM_011539982.1:c.1007A=	XP_011538284.1:p.Asp336=
XR_945791.1:n.1673A=
NM_000314.7:c.1103A=	NP_000305.3:p.Asp368=
NM_001304717.5:c.1622A=	NP_001291646.4:p.Asp541=
NM_001304718.2:c.512A=	NP_001291647.1:p.Asp171=
NM_000314.8:c.1103A= MANE Select	NP_000305.3:p.Asp368=