Canonical Allele Identifier: CA3174081312

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957914A= , CM000672.2:g.87957914A=	GRCh38
NC_000010.10:g.89717671A= , CM000672.1:g.89717671A=	GRCh37
NC_000010.9:g.89707651A=	NCBI36
NG_007466.2:g.99476A= , LRG_311:g.99476A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.696A=	ENSP00000514759.2:p.Thr232=
ENST00000710265.1:c.696A=	ENSP00000518161.1:p.Thr232=
ENST00000472832.3:c.696A=	ENSP00000483066.2:p.Thr232=
ENST00000688158.2:n.1431A=
ENST00000688922.2:c.*526A=	ENSP00000508742.2:n.*526A=
ENST00000700021.1:c.651A=	ENSP00000514757.1:p.Thr217=
ENST00000700022.1:c.*35A=	ENSP00000514758.1:n.*35A=
ENST00000700023.1:n.1854A=
ENST00000700024.1:n.2088A=
ENST00000700025.1:n.1465A=
ENST00000700026.1:n.333A=
ENST00000700029.1:c.530A=
ENST00000706954.1:c.696A=	ENSP00000516674.1:p.Thr232=
ENST00000706955.1:c.*731A=	ENSP00000516675.1:n.*731A=
ENST00000686459.1:c.*282A=	ENSP00000508909.1:n.*282A=
ENST00000688158.1:c.*807A=	ENSP00000509254.1:n.*807A=
ENST00000688308.1:c.696A=	ENSP00000508752.1:p.Thr232=
ENST00000688922.1:c.617A=
ENST00000693560.1:c.1215A=	ENSP00000509861.1:p.Thr405=
ENST00000371953.8:c.696A= MANE Select	ENSP00000361021.3:p.Thr232=
ENST00000371953.7:c.696A=	ENSP00000361021.3:p.Thr232=
ENST00000472832.2:c.123A=	ENSP00000483066.1:p.Thr41=
NM_000314.5:c.696A=	NP_000305.3:p.Thr232=
NM_000314.6:c.696A=	NP_000305.3:p.Thr232=
NM_001304717.2:c.1215A=	NP_001291646.2:p.Thr405=
NM_001304718.1:c.105A=	NP_001291647.1:p.Thr35=
XM_006717926.2:c.651A=	XP_006717989.1:p.Thr217=
XM_011539981.1:c.696A=	XP_011538283.1:p.Thr232=
XM_011539982.1:c.600A=	XP_011538284.1:p.Thr200=
XR_945791.1:n.1266A=
NM_000314.7:c.696A=	NP_000305.3:p.Thr232=
NM_001304717.5:c.1215A=	NP_001291646.4:p.Thr405=
NM_001304718.2:c.105A=	NP_001291647.1:p.Thr35=
NM_000314.8:c.696A= MANE Select	NP_000305.3:p.Thr232=