Canonical Allele Identifier: CA891835142

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960955_87960956delinsTT , CM000672.2:g.87960955_87960956delinsTT	GRCh38
NC_000010.10:g.89720712_89720713delinsTT , CM000672.1:g.89720712_89720713delinsTT	GRCh37
NC_000010.9:g.89710692_89710693delinsTT	NCBI36
NG_007466.2:g.102517_102518delinsTT , LRG_311:g.102517_102518delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.956_957delinsTT	ENSP00000514759.2:p.Glu319Val
ENST00000710265.1:c.863_864delinsTT	ENSP00000518161.1:p.Glu288Val
ENST00000472832.3:c.863_864delinsTT	ENSP00000483066.2:p.Glu288Val
ENST00000688158.2:n.1598_1599delinsTT
ENST00000688922.2:c.*693_*694delinsTT	ENSP00000508742.2:n.*693_*694delinsTT
ENST00000700021.1:c.818_819delinsTT	ENSP00000514757.1:p.Glu273Val
ENST00000700022.1:c.*202_*203delinsTT	ENSP00000514758.1:n.*202_*203delinsTT
ENST00000700023.1:n.2021_2022delinsTT
ENST00000700024.1:n.2255_2256delinsTT
ENST00000700025.1:n.1632_1633delinsTT
ENST00000700026.1:n.500_501delinsTT
ENST00000700029.1:c.790_791delinsTT
ENST00000706954.1:c.863_864delinsTT	ENSP00000516674.1:p.Glu288Val
ENST00000706955.1:c.*898_*899delinsTT	ENSP00000516675.1:n.*898_*899delinsTT
ENST00000686459.1:c.*449_*450delinsTT	ENSP00000508909.1:n.*449_*450delinsTT
ENST00000688158.1:c.*974_*975delinsTT	ENSP00000509254.1:n.*974_*975delinsTT
ENST00000688308.1:c.863_864delinsTT	ENSP00000508752.1:p.Glu288Val
ENST00000688922.1:c.784_785delinsTT
ENST00000693560.1:c.1382_1383delinsTT	ENSP00000509861.1:p.Glu461Val
ENST00000371953.8:c.863_864delinsTT MANE Select	ENSP00000361021.3:p.Glu288Val
ENST00000371953.7:c.863_864delinsTT	ENSP00000361021.3:p.Glu288Val
ENST00000472832.2:c.290_291delinsTT	ENSP00000483066.1:p.Glu97Val
NM_000314.5:c.863_864delinsTT	NP_000305.3:p.Glu288Val
NM_000314.6:c.863_864delinsTT	NP_000305.3:p.Glu288Val
NM_001304717.2:c.1382_1383delinsTT	NP_001291646.2:p.Glu461Val
NM_001304718.1:c.272_273delinsTT	NP_001291647.1:p.Glu91Val
XM_006717926.2:c.818_819delinsTT	XP_006717989.1:p.Glu273Val
XM_011539981.1:c.863_864delinsTT	XP_011538283.1:p.Glu288Val
XM_011539982.1:c.767_768delinsTT	XP_011538284.1:p.Glu256Val
XR_945791.1:n.1433_1434delinsTT
NM_000314.7:c.863_864delinsTT	NP_000305.3:p.Glu288Val
NM_001304717.5:c.1382_1383delinsTT	NP_001291646.4:p.Glu461Val
NM_001304718.2:c.272_273delinsTT	NP_001291647.1:p.Glu91Val
NM_000314.8:c.863_864delinsTT MANE Select	NP_000305.3:p.Glu288Val