Canonical Allele Identifier: CA891840956

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933117_87933118delinsCG , CM000672.2:g.87933117_87933118delinsCG	GRCh38
NC_000010.10:g.89692874_89692875delinsCG , CM000672.1:g.89692874_89692875delinsCG	GRCh37
NC_000010.9:g.89682854_89682855delinsCG	NCBI36
NG_007466.2:g.74679_74680delinsCG , LRG_311:g.74679_74680delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.358_359delinsCG	ENSP00000514759.2:p.Ala120Arg
ENST00000710265.1:c.358_359delinsCG	ENSP00000518161.1:p.Ala120Arg
ENST00000472832.3:c.358_359delinsCG	ENSP00000483066.2:p.Ala120Arg
ENST00000688158.2:n.1093_1094delinsCG
ENST00000688922.2:c.*188_*189delinsCG	ENSP00000508742.2:n.*188_*189delinsCG
ENST00000700021.1:c.313_314delinsCG	ENSP00000514757.1:p.Ala105Arg
ENST00000700022.1:c.358_359delinsCG	ENSP00000514758.1:p.Ala120Arg
ENST00000700029.1:c.192_193delinsCG
ENST00000706954.1:c.358_359delinsCG	ENSP00000516674.1:p.Ala120Arg
ENST00000706955.1:c.*393_*394delinsCG	ENSP00000516675.1:n.*393_*394delinsCG
ENST00000686459.1:c.358_359delinsCG	ENSP00000508909.1:p.Ala120Arg
ENST00000688158.1:c.*469_*470delinsCG	ENSP00000509254.1:n.*469_*470delinsCG
ENST00000688308.1:c.358_359delinsCG	ENSP00000508752.1:p.Ala120Arg
ENST00000688922.1:c.279_280delinsCG
ENST00000693560.1:c.877_878delinsCG	ENSP00000509861.1:p.Ala293Arg
ENST00000371953.8:c.358_359delinsCG MANE Select	ENSP00000361021.3:p.Ala120Arg
ENST00000371953.7:c.358_359delinsCG	ENSP00000361021.3:p.Ala120Arg
ENST00000498703.1:n.184_185delinsCG
ENST00000610634.1:c.256_257delinsCG	ENSP00000477517.1:p.Ala86Arg
NM_000314.5:c.358_359delinsCG	NP_000305.3:p.Ala120Arg
NM_000314.6:c.358_359delinsCG	NP_000305.3:p.Ala120Arg
NM_001304717.2:c.877_878delinsCG	NP_001291646.2:p.Ala293Arg
NM_001304718.1:c.-393_-392delinsCG	NP_001291647.1:n.-393_-392delinsCG
XM_006717926.2:c.313_314delinsCG	XP_006717989.1:p.Ala105Arg
XM_011539981.1:c.358_359delinsCG	XP_011538283.1:p.Ala120Arg
XM_011539982.1:c.262_263delinsCG	XP_011538284.1:p.Ala88Arg
XR_945789.1:n.1070_1071delinsCG
XR_945790.1:n.1070_1071delinsCG
XR_945791.1:n.1070_1071delinsCG
NM_000314.7:c.358_359delinsCG	NP_000305.3:p.Ala120Arg
NM_001304717.5:c.877_878delinsCG	NP_001291646.4:p.Ala293Arg
NM_001304718.2:c.-393_-392delinsCG	NP_001291647.1:n.-393_-392delinsCG
NM_000314.8:c.358_359delinsCG MANE Select	NP_000305.3:p.Ala120Arg