Canonical Allele Identifier: CA1926163894

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87926336T= , CM000672.2:g.87926336T=	GRCh38
NC_000010.10:g.89686093T= , CM000672.1:g.89686093T=	GRCh37
NC_000010.9:g.89676073T=	NCBI36
NG_007466.2:g.67898T= , LRG_311:g.67898T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.209+779T=	ENSP00000514759.2:n.209+779T=
ENST00000710265.1:c.209+779T=	ENSP00000518161.1:n.209+779T=
ENST00000472832.3:c.209+779T=	ENSP00000483066.2:n.209+779T=
ENST00000688158.2:n.944+779T=
ENST00000688922.2:c.209+779T=	ENSP00000508742.2:n.209+779T=
ENST00000700021.1:c.165-4710T=	ENSP00000514757.1:n.165-4710T=
ENST00000700022.1:c.209+779T=	ENSP00000514758.1:n.209+779T=
ENST00000700029.1:c.43+779T=
ENST00000706954.1:c.209+779T=	ENSP00000516674.1:n.209+779T=
ENST00000706955.1:c.*244+779T=	ENSP00000516675.1:n.*244+779T=
ENST00000686459.1:c.209+779T=	ENSP00000508909.1:n.209+779T=
ENST00000688158.1:c.*320+779T=	ENSP00000509254.1:n.*320+779T=
ENST00000688308.1:c.209+779T=	ENSP00000508752.1:n.209+779T=
ENST00000688922.1:c.78+779T=
ENST00000693560.1:c.728+779T=	ENSP00000509861.1:n.728+779T=
ENST00000371953.8:c.209+779T= MANE Select	ENSP00000361021.3:n.209+779T=
ENST00000371953.7:c.209+779T=	ENSP00000361021.3:n.209+779T=
ENST00000498703.1:n.35+779T=
ENST00000610634.1:c.107+779T=	ENSP00000477517.1:n.107+779T=
NM_000314.5:c.209+779T=	NP_000305.3:n.209+779T=
NM_000314.6:c.209+779T=	NP_000305.3:n.209+779T=
NM_001304717.2:c.728+779T=	NP_001291646.2:n.728+779T=
NM_001304718.1:c.-541-4710T=	NP_001291647.1:n.-541-4710T=
XM_006717926.2:c.165-4710T=	XP_006717989.1:n.165-4710T=
XM_011539981.1:c.209+779T=	XP_011538283.1:n.209+779T=
XM_011539982.1:c.113+779T=	XP_011538284.1:n.113+779T=
XR_945789.1:n.921+779T=
XR_945790.1:n.921+779T=
XR_945791.1:n.921+779T=
NM_000314.7:c.209+779T=	NP_000305.3:n.209+779T=
NM_001304717.5:c.728+779T=	NP_001291646.4:n.728+779T=
NM_001304718.2:c.-541-4710T=	NP_001291647.1:n.-541-4710T=
NM_000314.8:c.209+779T= MANE Select	NP_000305.3:n.209+779T=