Canonical Allele Identifier: CA1926189962

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960920T= , CM000672.2:g.87960920T=	GRCh38
NC_000010.10:g.89720677T= , CM000672.1:g.89720677T=	GRCh37
NC_000010.9:g.89710657T=	NCBI36
NG_007466.2:g.102482T= , LRG_311:g.102482T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.921T=	ENSP00000514759.2:p.Asn307=
ENST00000710265.1:c.828T=	ENSP00000518161.1:p.Asn276=
ENST00000472832.3:c.828T=	ENSP00000483066.2:p.Asn276=
ENST00000688158.2:n.1563T=
ENST00000688922.2:c.*658T=	ENSP00000508742.2:n.*658T=
ENST00000700021.1:c.783T=	ENSP00000514757.1:p.Asn261=
ENST00000700022.1:c.*167T=	ENSP00000514758.1:n.*167T=
ENST00000700023.1:n.1986T=
ENST00000700024.1:n.2220T=
ENST00000700025.1:n.1597T=
ENST00000700026.1:n.465T=
ENST00000700029.1:c.755T=
ENST00000706954.1:c.828T=	ENSP00000516674.1:p.Asn276=
ENST00000706955.1:c.*863T=	ENSP00000516675.1:n.*863T=
ENST00000686459.1:c.*414T=	ENSP00000508909.1:n.*414T=
ENST00000688158.1:c.*939T=	ENSP00000509254.1:n.*939T=
ENST00000688308.1:c.828T=	ENSP00000508752.1:p.Asn276=
ENST00000688922.1:c.749T=
ENST00000693560.1:c.1347T=	ENSP00000509861.1:p.Asn449=
ENST00000371953.8:c.828T= MANE Select	ENSP00000361021.3:p.Asn276=
ENST00000371953.7:c.828T=	ENSP00000361021.3:p.Asn276=
ENST00000472832.2:c.255T=	ENSP00000483066.1:p.Asn85=
NM_000314.5:c.828T=	NP_000305.3:p.Asn276=
NM_000314.6:c.828T=	NP_000305.3:p.Asn276=
NM_001304717.2:c.1347T=	NP_001291646.2:p.Asn449=
NM_001304718.1:c.237T=	NP_001291647.1:p.Asn79=
XM_006717926.2:c.783T=	XP_006717989.1:p.Asn261=
XM_011539981.1:c.828T=	XP_011538283.1:p.Asn276=
XM_011539982.1:c.732T=	XP_011538284.1:p.Asn244=
XR_945791.1:n.1398T=
NM_000314.7:c.828T=	NP_000305.3:p.Asn276=
NM_001304717.5:c.1347T=	NP_001291646.4:p.Asn449=
NM_001304718.2:c.237T=	NP_001291647.1:p.Asn79=
NM_000314.8:c.828T= MANE Select	NP_000305.3:p.Asn276=