Canonical Allele Identifier: CA891834997

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960946_87960947delinsTT , CM000672.2:g.87960946_87960947delinsTT	GRCh38
NC_000010.10:g.89720703_89720704delinsTT , CM000672.1:g.89720703_89720704delinsTT	GRCh37
NC_000010.9:g.89710683_89710684delinsTT	NCBI36
NG_007466.2:g.102508_102509delinsTT , LRG_311:g.102508_102509delinsTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.947_948delinsTT	ENSP00000514759.2:p.Glu316Val
ENST00000710265.1:c.854_855delinsTT	ENSP00000518161.1:p.Glu285Val
ENST00000472832.3:c.854_855delinsTT	ENSP00000483066.2:p.Glu285Val
ENST00000688158.2:n.1589_1590delinsTT
ENST00000688922.2:c.*684_*685delinsTT	ENSP00000508742.2:n.*684_*685delinsTT
ENST00000700021.1:c.809_810delinsTT	ENSP00000514757.1:p.Glu270Val
ENST00000700022.1:c.*193_*194delinsTT	ENSP00000514758.1:n.*193_*194delinsTT
ENST00000700023.1:n.2012_2013delinsTT
ENST00000700024.1:n.2246_2247delinsTT
ENST00000700025.1:n.1623_1624delinsTT
ENST00000700026.1:n.491_492delinsTT
ENST00000700029.1:c.781_782delinsTT
ENST00000706954.1:c.854_855delinsTT	ENSP00000516674.1:p.Glu285Val
ENST00000706955.1:c.*889_*890delinsTT	ENSP00000516675.1:n.*889_*890delinsTT
ENST00000686459.1:c.*440_*441delinsTT	ENSP00000508909.1:n.*440_*441delinsTT
ENST00000688158.1:c.*965_*966delinsTT	ENSP00000509254.1:n.*965_*966delinsTT
ENST00000688308.1:c.854_855delinsTT	ENSP00000508752.1:p.Glu285Val
ENST00000688922.1:c.775_776delinsTT
ENST00000693560.1:c.1373_1374delinsTT	ENSP00000509861.1:p.Glu458Val
ENST00000371953.8:c.854_855delinsTT MANE Select	ENSP00000361021.3:p.Glu285Val
ENST00000371953.7:c.854_855delinsTT	ENSP00000361021.3:p.Glu285Val
ENST00000472832.2:c.281_282delinsTT	ENSP00000483066.1:p.Glu94Val
NM_000314.5:c.854_855delinsTT	NP_000305.3:p.Glu285Val
NM_000314.6:c.854_855delinsTT	NP_000305.3:p.Glu285Val
NM_001304717.2:c.1373_1374delinsTT	NP_001291646.2:p.Glu458Val
NM_001304718.1:c.263_264delinsTT	NP_001291647.1:p.Glu88Val
XM_006717926.2:c.809_810delinsTT	XP_006717989.1:p.Glu270Val
XM_011539981.1:c.854_855delinsTT	XP_011538283.1:p.Glu285Val
XM_011539982.1:c.758_759delinsTT	XP_011538284.1:p.Glu253Val
XR_945791.1:n.1424_1425delinsTT
NM_000314.7:c.854_855delinsTT	NP_000305.3:p.Glu285Val
NM_001304717.5:c.1373_1374delinsTT	NP_001291646.4:p.Glu458Val
NM_001304718.2:c.263_264delinsTT	NP_001291647.1:p.Glu88Val
NM_000314.8:c.854_855delinsTT MANE Select	NP_000305.3:p.Glu285Val