Canonical Allele Identifier: CA891835140

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960955_87960956delinsCT , CM000672.2:g.87960955_87960956delinsCT	GRCh38
NC_000010.10:g.89720712_89720713delinsCT , CM000672.1:g.89720712_89720713delinsCT	GRCh37
NC_000010.9:g.89710692_89710693delinsCT	NCBI36
NG_007466.2:g.102517_102518delinsCT , LRG_311:g.102517_102518delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.956_957delinsCT	ENSP00000514759.2:p.Glu319Ala
ENST00000710265.1:c.863_864delinsCT	ENSP00000518161.1:p.Glu288Ala
ENST00000472832.3:c.863_864delinsCT	ENSP00000483066.2:p.Glu288Ala
ENST00000688158.2:n.1598_1599delinsCT
ENST00000688922.2:c.*693_*694delinsCT	ENSP00000508742.2:n.*693_*694delinsCT
ENST00000700021.1:c.818_819delinsCT	ENSP00000514757.1:p.Glu273Ala
ENST00000700022.1:c.*202_*203delinsCT	ENSP00000514758.1:n.*202_*203delinsCT
ENST00000700023.1:n.2021_2022delinsCT
ENST00000700024.1:n.2255_2256delinsCT
ENST00000700025.1:n.1632_1633delinsCT
ENST00000700026.1:n.500_501delinsCT
ENST00000700029.1:c.790_791delinsCT
ENST00000706954.1:c.863_864delinsCT	ENSP00000516674.1:p.Glu288Ala
ENST00000706955.1:c.*898_*899delinsCT	ENSP00000516675.1:n.*898_*899delinsCT
ENST00000686459.1:c.*449_*450delinsCT	ENSP00000508909.1:n.*449_*450delinsCT
ENST00000688158.1:c.*974_*975delinsCT	ENSP00000509254.1:n.*974_*975delinsCT
ENST00000688308.1:c.863_864delinsCT	ENSP00000508752.1:p.Glu288Ala
ENST00000688922.1:c.784_785delinsCT
ENST00000693560.1:c.1382_1383delinsCT	ENSP00000509861.1:p.Glu461Ala
ENST00000371953.8:c.863_864delinsCT MANE Select	ENSP00000361021.3:p.Glu288Ala
ENST00000371953.7:c.863_864delinsCT	ENSP00000361021.3:p.Glu288Ala
ENST00000472832.2:c.290_291delinsCT	ENSP00000483066.1:p.Glu97Ala
NM_000314.5:c.863_864delinsCT	NP_000305.3:p.Glu288Ala
NM_000314.6:c.863_864delinsCT	NP_000305.3:p.Glu288Ala
NM_001304717.2:c.1382_1383delinsCT	NP_001291646.2:p.Glu461Ala
NM_001304718.1:c.272_273delinsCT	NP_001291647.1:p.Glu91Ala
XM_006717926.2:c.818_819delinsCT	XP_006717989.1:p.Glu273Ala
XM_011539981.1:c.863_864delinsCT	XP_011538283.1:p.Glu288Ala
XM_011539982.1:c.767_768delinsCT	XP_011538284.1:p.Glu256Ala
XR_945791.1:n.1433_1434delinsCT
NM_000314.7:c.863_864delinsCT	NP_000305.3:p.Glu288Ala
NM_001304717.5:c.1382_1383delinsCT	NP_001291646.4:p.Glu461Ala
NM_001304718.2:c.272_273delinsCT	NP_001291647.1:p.Glu91Ala
NM_000314.8:c.863_864delinsCT MANE Select	NP_000305.3:p.Glu288Ala