Canonical Allele Identifier: CA891835236

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960963_87960965delinsTGT , CM000672.2:g.87960963_87960965delinsTGT	GRCh38
NC_000010.10:g.89720720_89720722delinsTGT , CM000672.1:g.89720720_89720722delinsTGT	GRCh37
NC_000010.9:g.89710700_89710702delinsTGT	NCBI36
NG_007466.2:g.102525_102527delinsTGT , LRG_311:g.102525_102527delinsTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.964_966delinsTGT	ENSP00000514759.2:p.Glu322Cys
ENST00000710265.1:c.871_873delinsTGT	ENSP00000518161.1:p.Glu291Cys
ENST00000472832.3:c.871_873delinsTGT	ENSP00000483066.2:p.Glu291Cys
ENST00000688158.2:n.1606_1608delinsTGT
ENST00000688922.2:c.*701_*703delinsTGT	ENSP00000508742.2:n.*701_*703delinsTGT
ENST00000700021.1:c.826_828delinsTGT	ENSP00000514757.1:p.Glu276Cys
ENST00000700022.1:c.*210_*212delinsTGT	ENSP00000514758.1:n.*210_*212delinsTGT
ENST00000700023.1:n.2029_2031delinsTGT
ENST00000700024.1:n.2263_2265delinsTGT
ENST00000700025.1:n.1640_1642delinsTGT
ENST00000700026.1:n.508_510delinsTGT
ENST00000700029.1:c.798_800delinsTGT
ENST00000706954.1:c.871_873delinsTGT	ENSP00000516674.1:p.Glu291Cys
ENST00000706955.1:c.*906_*908delinsTGT	ENSP00000516675.1:n.*906_*908delinsTGT
ENST00000686459.1:c.*457_*459delinsTGT	ENSP00000508909.1:n.*457_*459delinsTGT
ENST00000688158.1:c.*982_*984delinsTGT	ENSP00000509254.1:n.*982_*984delinsTGT
ENST00000688308.1:c.871_873delinsTGT	ENSP00000508752.1:p.Glu291Cys
ENST00000688922.1:c.792_794delinsTGT
ENST00000693560.1:c.1390_1392delinsTGT	ENSP00000509861.1:p.Glu464Cys
ENST00000371953.8:c.871_873delinsTGT MANE Select	ENSP00000361021.3:p.Glu291Cys
ENST00000371953.7:c.871_873delinsTGT	ENSP00000361021.3:p.Glu291Cys
ENST00000472832.2:c.298_300delinsTGT	ENSP00000483066.1:p.Glu100Cys
NM_000314.5:c.871_873delinsTGT	NP_000305.3:p.Glu291Cys
NM_000314.6:c.871_873delinsTGT	NP_000305.3:p.Glu291Cys
NM_001304717.2:c.1390_1392delinsTGT	NP_001291646.2:p.Glu464Cys
NM_001304718.1:c.280_282delinsTGT	NP_001291647.1:p.Glu94Cys
XM_006717926.2:c.826_828delinsTGT	XP_006717989.1:p.Glu276Cys
XM_011539981.1:c.871_873delinsTGT	XP_011538283.1:p.Glu291Cys
XM_011539982.1:c.775_777delinsTGT	XP_011538284.1:p.Glu259Cys
XR_945791.1:n.1441_1443delinsTGT
NM_000314.7:c.871_873delinsTGT	NP_000305.3:p.Glu291Cys
NM_001304717.5:c.1390_1392delinsTGT	NP_001291646.4:p.Glu464Cys
NM_001304718.2:c.280_282delinsTGT	NP_001291647.1:p.Glu94Cys
NM_000314.8:c.871_873delinsTGT MANE Select	NP_000305.3:p.Glu291Cys