Canonical Allele Identifier: CA1926189988

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960952C= , CM000672.2:g.87960952C=	GRCh38
NC_000010.10:g.89720709C= , CM000672.1:g.89720709C=	GRCh37
NC_000010.9:g.89710689C=	NCBI36
NG_007466.2:g.102514C= , LRG_311:g.102514C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.953C=	ENSP00000514759.2:p.Ser318=
ENST00000710265.1:c.860C=	ENSP00000518161.1:p.Ser287=
ENST00000472832.3:c.860C=	ENSP00000483066.2:p.Ser287=
ENST00000688158.2:n.1595C=
ENST00000688922.2:c.*690C=	ENSP00000508742.2:n.*690C=
ENST00000700021.1:c.815C=	ENSP00000514757.1:p.Ser272=
ENST00000700022.1:c.*199C=	ENSP00000514758.1:n.*199C=
ENST00000700023.1:n.2018C=
ENST00000700024.1:n.2252C=
ENST00000700025.1:n.1629C=
ENST00000700026.1:n.497C=
ENST00000700029.1:c.787C=
ENST00000706954.1:c.860C=	ENSP00000516674.1:p.Ser287=
ENST00000706955.1:c.*895C=	ENSP00000516675.1:n.*895C=
ENST00000686459.1:c.*446C=	ENSP00000508909.1:n.*446C=
ENST00000688158.1:c.*971C=	ENSP00000509254.1:n.*971C=
ENST00000688308.1:c.860C=	ENSP00000508752.1:p.Ser287=
ENST00000688922.1:c.781C=
ENST00000693560.1:c.1379C=	ENSP00000509861.1:p.Ser460=
ENST00000371953.8:c.860C= MANE Select	ENSP00000361021.3:p.Ser287=
ENST00000371953.7:c.860C=	ENSP00000361021.3:p.Ser287=
ENST00000472832.2:c.287C=	ENSP00000483066.1:p.Ser96=
NM_000314.5:c.860C=	NP_000305.3:p.Ser287=
NM_000314.6:c.860C=	NP_000305.3:p.Ser287=
NM_001304717.2:c.1379C=	NP_001291646.2:p.Ser460=
NM_001304718.1:c.269C=	NP_001291647.1:p.Ser90=
XM_006717926.2:c.815C=	XP_006717989.1:p.Ser272=
XM_011539981.1:c.860C=	XP_011538283.1:p.Ser287=
XM_011539982.1:c.764C=	XP_011538284.1:p.Ser255=
XR_945791.1:n.1430C=
NM_000314.7:c.860C=	NP_000305.3:p.Ser287=
NM_001304717.5:c.1379C=	NP_001291646.4:p.Ser460=
NM_001304718.2:c.269C=	NP_001291647.1:p.Ser90=
NM_000314.8:c.860C= MANE Select	NP_000305.3:p.Ser287=