Canonical Allele Identifier: CA1926189951

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960911T= , CM000672.2:g.87960911T=	GRCh38
NC_000010.10:g.89720668T= , CM000672.1:g.89720668T=	GRCh37
NC_000010.9:g.89710648T=	NCBI36
NG_007466.2:g.102473T= , LRG_311:g.102473T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.912T=	ENSP00000514759.2:p.Phe304=
ENST00000710265.1:c.819T=	ENSP00000518161.1:p.Phe273=
ENST00000472832.3:c.819T=	ENSP00000483066.2:p.Phe273=
ENST00000688158.2:n.1554T=
ENST00000688922.2:c.*649T=	ENSP00000508742.2:n.*649T=
ENST00000700021.1:c.774T=	ENSP00000514757.1:p.Phe258=
ENST00000700022.1:c.*158T=	ENSP00000514758.1:n.*158T=
ENST00000700023.1:n.1977T=
ENST00000700024.1:n.2211T=
ENST00000700025.1:n.1588T=
ENST00000700026.1:n.456T=
ENST00000700029.1:c.746T=
ENST00000706954.1:c.819T=	ENSP00000516674.1:p.Phe273=
ENST00000706955.1:c.*854T=	ENSP00000516675.1:n.*854T=
ENST00000686459.1:c.*405T=	ENSP00000508909.1:n.*405T=
ENST00000688158.1:c.*930T=	ENSP00000509254.1:n.*930T=
ENST00000688308.1:c.819T=	ENSP00000508752.1:p.Phe273=
ENST00000688922.1:c.740T=
ENST00000693560.1:c.1338T=	ENSP00000509861.1:p.Phe446=
ENST00000371953.8:c.819T= MANE Select	ENSP00000361021.3:p.Phe273=
ENST00000371953.7:c.819T=	ENSP00000361021.3:p.Phe273=
ENST00000472832.2:c.246T=	ENSP00000483066.1:p.Phe82=
NM_000314.5:c.819T=	NP_000305.3:p.Phe273=
NM_000314.6:c.819T=	NP_000305.3:p.Phe273=
NM_001304717.2:c.1338T=	NP_001291646.2:p.Phe446=
NM_001304718.1:c.228T=	NP_001291647.1:p.Phe76=
XM_006717926.2:c.774T=	XP_006717989.1:p.Phe258=
XM_011539981.1:c.819T=	XP_011538283.1:p.Phe273=
XM_011539982.1:c.723T=	XP_011538284.1:p.Phe241=
XR_945791.1:n.1389T=
NM_000314.7:c.819T=	NP_000305.3:p.Phe273=
NM_001304717.5:c.1338T=	NP_001291646.4:p.Phe446=
NM_001304718.2:c.228T=	NP_001291647.1:p.Phe76=
NM_000314.8:c.819T= MANE Select	NP_000305.3:p.Phe273=