Canonical Allele Identifier: CA2497028760

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952254C= , CM000672.2:g.87952254C=	GRCh38
NC_000010.10:g.89712011C= , CM000672.1:g.89712011C=	GRCh37
NC_000010.9:g.89701991C=	NCBI36
NG_007466.2:g.93816C= , LRG_311:g.93816C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000314.8:c.629C= MANE Select	NP_000305.3:p.Thr210=
ENST00000371953.8:c.629C= MANE Select	ENSP00000361021.3:p.Thr210=
NM_000314.5:c.629C=	NP_000305.3:p.Thr210=
NM_000314.6:c.629C=	NP_000305.3:p.Thr210=
NM_000314.7:c.629C=	NP_000305.3:p.Thr210=
NM_001304717.2:c.1148C=	NP_001291646.2:p.Thr383=
NM_001304717.5:c.1148C=	NP_001291646.4:p.Thr383=
NM_001304718.1:c.38C=	NP_001291647.1:p.Thr13=
NM_001304718.2:c.38C=	NP_001291647.1:p.Thr13=
ENST00000371953.7:c.629C=	ENSP00000361021.3:p.Thr210=
ENST00000472832.2:c.56C=	ENSP00000483066.1:p.Thr19=
ENST00000472832.3:c.629C=	ENSP00000483066.2:p.Thr210=
ENST00000686459.1:c.*215C=	ENSP00000508909.1:n.*215C=
ENST00000688158.1:c.*740C=	ENSP00000509254.1:n.*740C=
ENST00000688158.2:n.1364C=
ENST00000688308.1:c.629C=	ENSP00000508752.1:p.Thr210=
ENST00000688922.1:c.550C=
ENST00000688922.2:c.*459C=	ENSP00000508742.2:n.*459C=
ENST00000693560.1:c.1148C=	ENSP00000509861.1:p.Thr383=
ENST00000700021.1:c.584C=	ENSP00000514757.1:p.Thr195=
ENST00000700022.1:c.493-5599C=	ENSP00000514758.1:n.493-5599C=
ENST00000700023.1:n.1787C=
ENST00000700024.1:n.2021C=
ENST00000700025.1:n.1398C=
ENST00000700029.1:c.463C=
ENST00000700029.2:c.629C=	ENSP00000514759.2:p.Thr210=
ENST00000706954.1:c.629C=	ENSP00000516674.1:p.Thr210=
ENST00000706955.1:c.*664C=	ENSP00000516675.1:n.*664C=
ENST00000710265.1:c.629C=	ENSP00000518161.1:p.Thr210=
XM_006717926.2:c.584C=	XP_006717989.1:p.Thr195=
XM_011539981.1:c.629C=	XP_011538283.1:p.Thr210=
XM_011539982.1:c.533C=	XP_011538284.1:p.Thr178=
XR_945791.1:n.1205-5599C=