Canonical Allele Identifier: CA891834982

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960945_87960947delinsACT , CM000672.2:g.87960945_87960947delinsACT	GRCh38
NC_000010.10:g.89720702_89720704delinsACT , CM000672.1:g.89720702_89720704delinsACT	GRCh37
NC_000010.9:g.89710682_89710684delinsACT	NCBI36
NG_007466.2:g.102507_102509delinsACT , LRG_311:g.102507_102509delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.946_948delinsACT	ENSP00000514759.2:p.Glu316Thr
ENST00000710265.1:c.853_855delinsACT	ENSP00000518161.1:p.Glu285Thr
ENST00000472832.3:c.853_855delinsACT	ENSP00000483066.2:p.Glu285Thr
ENST00000688158.2:n.1588_1590delinsACT
ENST00000688922.2:c.*683_*685delinsACT	ENSP00000508742.2:n.*683_*685delinsACT
ENST00000700021.1:c.808_810delinsACT	ENSP00000514757.1:p.Glu270Thr
ENST00000700022.1:c.*192_*194delinsACT	ENSP00000514758.1:n.*192_*194delinsACT
ENST00000700023.1:n.2011_2013delinsACT
ENST00000700024.1:n.2245_2247delinsACT
ENST00000700025.1:n.1622_1624delinsACT
ENST00000700026.1:n.490_492delinsACT
ENST00000700029.1:c.780_782delinsACT
ENST00000706954.1:c.853_855delinsACT	ENSP00000516674.1:p.Glu285Thr
ENST00000706955.1:c.*888_*890delinsACT	ENSP00000516675.1:n.*888_*890delinsACT
ENST00000686459.1:c.*439_*441delinsACT	ENSP00000508909.1:n.*439_*441delinsACT
ENST00000688158.1:c.*964_*966delinsACT	ENSP00000509254.1:n.*964_*966delinsACT
ENST00000688308.1:c.853_855delinsACT	ENSP00000508752.1:p.Glu285Thr
ENST00000688922.1:c.774_776delinsACT
ENST00000693560.1:c.1372_1374delinsACT	ENSP00000509861.1:p.Glu458Thr
ENST00000371953.8:c.853_855delinsACT MANE Select	ENSP00000361021.3:p.Glu285Thr
ENST00000371953.7:c.853_855delinsACT	ENSP00000361021.3:p.Glu285Thr
ENST00000472832.2:c.280_282delinsACT	ENSP00000483066.1:p.Glu94Thr
NM_000314.5:c.853_855delinsACT	NP_000305.3:p.Glu285Thr
NM_000314.6:c.853_855delinsACT	NP_000305.3:p.Glu285Thr
NM_001304717.2:c.1372_1374delinsACT	NP_001291646.2:p.Glu458Thr
NM_001304718.1:c.262_264delinsACT	NP_001291647.1:p.Glu88Thr
XM_006717926.2:c.808_810delinsACT	XP_006717989.1:p.Glu270Thr
XM_011539981.1:c.853_855delinsACT	XP_011538283.1:p.Glu285Thr
XM_011539982.1:c.757_759delinsACT	XP_011538284.1:p.Glu253Thr
XR_945791.1:n.1423_1425delinsACT
NM_000314.7:c.853_855delinsACT	NP_000305.3:p.Glu285Thr
NM_001304717.5:c.1372_1374delinsACT	NP_001291646.4:p.Glu458Thr
NM_001304718.2:c.262_264delinsACT	NP_001291647.1:p.Glu88Thr
NM_000314.8:c.853_855delinsACT MANE Select	NP_000305.3:p.Glu285Thr