Canonical Allele Identifier: CA891836119

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961014_87961016delinsGAA , CM000672.2:g.87961014_87961016delinsGAA	GRCh38
NC_000010.10:g.89720771_89720773delinsGAA , CM000672.1:g.89720771_89720773delinsGAA	GRCh37
NC_000010.9:g.89710751_89710753delinsGAA	NCBI36
NG_007466.2:g.102576_102578delinsGAA , LRG_311:g.102576_102578delinsGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1015_1017delinsGAA	ENSP00000514759.2:p.Arg339Glu
ENST00000710265.1:c.922_924delinsGAA	ENSP00000518161.1:p.Arg308Glu
ENST00000472832.3:c.922_924delinsGAA	ENSP00000483066.2:p.Arg308Glu
ENST00000688158.2:n.1657_1659delinsGAA
ENST00000688922.2:c.*752_*754delinsGAA	ENSP00000508742.2:n.*752_*754delinsGAA
ENST00000700021.1:c.877_879delinsGAA	ENSP00000514757.1:p.Arg293Glu
ENST00000700022.1:c.*261_*263delinsGAA	ENSP00000514758.1:n.*261_*263delinsGAA
ENST00000700023.1:n.2080_2082delinsGAA
ENST00000700024.1:n.2314_2316delinsGAA
ENST00000700025.1:n.1691_1693delinsGAA
ENST00000700026.1:n.559_561delinsGAA
ENST00000706954.1:c.922_924delinsGAA	ENSP00000516674.1:p.Arg308Glu
ENST00000706955.1:c.*957_*959delinsGAA	ENSP00000516675.1:n.*957_*959delinsGAA
ENST00000686459.1:c.*508_*510delinsGAA	ENSP00000508909.1:n.*508_*510delinsGAA
ENST00000688158.1:c.*1033_*1035delinsGAA	ENSP00000509254.1:n.*1033_*1035delinsGAA
ENST00000688308.1:c.922_924delinsGAA	ENSP00000508752.1:p.Arg308Glu
ENST00000688922.1:c.843_845delinsGAA
ENST00000693560.1:c.1441_1443delinsGAA	ENSP00000509861.1:p.Arg481Glu
ENST00000371953.8:c.922_924delinsGAA MANE Select	ENSP00000361021.3:p.Arg308Glu
ENST00000371953.7:c.922_924delinsGAA	ENSP00000361021.3:p.Arg308Glu
ENST00000472832.2:c.349_351delinsGAA	ENSP00000483066.1:p.Arg117Glu
NM_000314.5:c.922_924delinsGAA	NP_000305.3:p.Arg308Glu
NM_000314.6:c.922_924delinsGAA	NP_000305.3:p.Arg308Glu
NM_001304717.2:c.1441_1443delinsGAA	NP_001291646.2:p.Arg481Glu
NM_001304718.1:c.331_333delinsGAA	NP_001291647.1:p.Arg111Glu
XM_006717926.2:c.877_879delinsGAA	XP_006717989.1:p.Arg293Glu
XM_011539981.1:c.922_924delinsGAA	XP_011538283.1:p.Arg308Glu
XM_011539982.1:c.826_828delinsGAA	XP_011538284.1:p.Arg276Glu
XR_945791.1:n.1492_1494delinsGAA
NM_000314.7:c.922_924delinsGAA	NP_000305.3:p.Arg308Glu
NM_001304717.5:c.1441_1443delinsGAA	NP_001291646.4:p.Arg481Glu
NM_001304718.2:c.331_333delinsGAA	NP_001291647.1:p.Arg111Glu
NM_000314.8:c.922_924delinsGAA MANE Select	NP_000305.3:p.Arg308Glu