Canonical Allele Identifier: CA3174440529

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933179A= , CM000672.2:g.87933179A=	GRCh38
NC_000010.10:g.89692936A= , CM000672.1:g.89692936A=	GRCh37
NC_000010.9:g.89682916A=	NCBI36
NG_007466.2:g.74741A= , LRG_311:g.74741A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.420A=	ENSP00000514759.2:p.Leu140=
ENST00000710265.1:c.420A=	ENSP00000518161.1:p.Leu140=
ENST00000472832.3:c.420A=	ENSP00000483066.2:p.Leu140=
ENST00000688158.2:n.1155A=
ENST00000688922.2:c.*250A=	ENSP00000508742.2:n.*250A=
ENST00000700021.1:c.375A=	ENSP00000514757.1:p.Leu125=
ENST00000700022.1:c.420A=	ENSP00000514758.1:p.Leu140=
ENST00000700029.1:c.254A=
ENST00000706954.1:c.420A=	ENSP00000516674.1:p.Leu140=
ENST00000706955.1:c.*455A=	ENSP00000516675.1:n.*455A=
ENST00000686459.1:c.420A=	ENSP00000508909.1:p.Leu140=
ENST00000688158.1:c.*531A=	ENSP00000509254.1:n.*531A=
ENST00000688308.1:c.420A=	ENSP00000508752.1:p.Leu140=
ENST00000688922.1:c.341A=
ENST00000693560.1:c.939A=	ENSP00000509861.1:p.Leu313=
ENST00000371953.8:c.420A= MANE Select	ENSP00000361021.3:p.Leu140=
ENST00000371953.7:c.420A=	ENSP00000361021.3:p.Leu140=
ENST00000498703.1:n.246A=
ENST00000610634.1:c.318A=	ENSP00000477517.1:p.Leu106=
NM_000314.5:c.420A=	NP_000305.3:p.Leu140=
NM_000314.6:c.420A=	NP_000305.3:p.Leu140=
NM_001304717.2:c.939A=	NP_001291646.2:p.Leu313=
NM_001304718.1:c.-331A=	NP_001291647.1:n.-331A=
XM_006717926.2:c.375A=	XP_006717989.1:p.Leu125=
XM_011539981.1:c.420A=	XP_011538283.1:p.Leu140=
XM_011539982.1:c.324A=	XP_011538284.1:p.Leu108=
XR_945789.1:n.1132A=
XR_945790.1:n.1132A=
XR_945791.1:n.1132A=
NM_000314.7:c.420A=	NP_000305.3:p.Leu140=
NM_001304717.5:c.939A=	NP_001291646.4:p.Leu313=
NM_001304718.2:c.-331A=	NP_001291647.1:n.-331A=
NM_000314.8:c.420A= MANE Select	NP_000305.3:p.Leu140=