Canonical Allele Identifier: CA891837669

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933145_87933146delinsCT , CM000672.2:g.87933145_87933146delinsCT	GRCh38
NC_000010.10:g.89692902_89692903delinsCT , CM000672.1:g.89692902_89692903delinsCT	GRCh37
NC_000010.9:g.89682882_89682883delinsCT	NCBI36
NG_007466.2:g.74707_74708delinsCT , LRG_311:g.74707_74708delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.386_387delinsCT	ENSP00000514759.2:p.Gly129Ala
ENST00000710265.1:c.386_387delinsCT	ENSP00000518161.1:p.Gly129Ala
ENST00000472832.3:c.386_387delinsCT	ENSP00000483066.2:p.Gly129Ala
ENST00000688158.2:n.1121_1122delinsCT
ENST00000688922.2:c.*216_*217delinsCT	ENSP00000508742.2:n.*216_*217delinsCT
ENST00000700021.1:c.341_342delinsCT	ENSP00000514757.1:p.Gly114Ala
ENST00000700022.1:c.386_387delinsCT	ENSP00000514758.1:p.Gly129Ala
ENST00000700029.1:c.220_221delinsCT
ENST00000706954.1:c.386_387delinsCT	ENSP00000516674.1:p.Gly129Ala
ENST00000706955.1:c.*421_*422delinsCT	ENSP00000516675.1:n.*421_*422delinsCT
ENST00000686459.1:c.386_387delinsCT	ENSP00000508909.1:p.Gly129Ala
ENST00000688158.1:c.*497_*498delinsCT	ENSP00000509254.1:n.*497_*498delinsCT
ENST00000688308.1:c.386_387delinsCT	ENSP00000508752.1:p.Gly129Ala
ENST00000688922.1:c.307_308delinsCT
ENST00000693560.1:c.905_906delinsCT	ENSP00000509861.1:p.Gly302Ala
ENST00000371953.8:c.386_387delinsCT MANE Select	ENSP00000361021.3:p.Gly129Ala
ENST00000371953.7:c.386_387delinsCT	ENSP00000361021.3:p.Gly129Ala
ENST00000498703.1:n.212_213delinsCT
ENST00000610634.1:c.284_285delinsCT	ENSP00000477517.1:p.Gly95Ala
NM_000314.5:c.386_387delinsCT	NP_000305.3:p.Gly129Ala
NM_000314.6:c.386_387delinsCT	NP_000305.3:p.Gly129Ala
NM_001304717.2:c.905_906delinsCT	NP_001291646.2:p.Gly302Ala
NM_001304718.1:c.-365_-364delinsCT	NP_001291647.1:n.-365_-364delinsCT
XM_006717926.2:c.341_342delinsCT	XP_006717989.1:p.Gly114Ala
XM_011539981.1:c.386_387delinsCT	XP_011538283.1:p.Gly129Ala
XM_011539982.1:c.290_291delinsCT	XP_011538284.1:p.Gly97Ala
XR_945789.1:n.1098_1099delinsCT
XR_945790.1:n.1098_1099delinsCT
XR_945791.1:n.1098_1099delinsCT
NM_000314.7:c.386_387delinsCT	NP_000305.3:p.Gly129Ala
NM_001304717.5:c.905_906delinsCT	NP_001291646.4:p.Gly302Ala
NM_001304718.2:c.-365_-364delinsCT	NP_001291647.1:n.-365_-364delinsCT
NM_000314.8:c.386_387delinsCT MANE Select	NP_000305.3:p.Gly129Ala