Canonical Allele Identifier: CA891841285

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961047_87961048delinsCT , CM000672.2:g.87961047_87961048delinsCT	GRCh38
NC_000010.10:g.89720804_89720805delinsCT , CM000672.1:g.89720804_89720805delinsCT	GRCh37
NC_000010.9:g.89710784_89710785delinsCT	NCBI36
NG_007466.2:g.102609_102610delinsCT , LRG_311:g.102609_102610delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1048_1049delinsCT	ENSP00000514759.2:p.Thr350Leu
ENST00000710265.1:c.955_956delinsCT	ENSP00000518161.1:p.Thr319Leu
ENST00000472832.3:c.955_956delinsCT	ENSP00000483066.2:p.Thr319Leu
ENST00000688158.2:n.1690_1691delinsCT
ENST00000688922.2:c.*785_*786delinsCT	ENSP00000508742.2:n.*785_*786delinsCT
ENST00000700021.1:c.910_911delinsCT	ENSP00000514757.1:p.Thr304Leu
ENST00000700022.1:c.*294_*295delinsCT	ENSP00000514758.1:n.*294_*295delinsCT
ENST00000700023.1:n.2113_2114delinsCT
ENST00000700024.1:n.2347_2348delinsCT
ENST00000700025.1:n.1724_1725delinsCT
ENST00000700026.1:n.592_593delinsCT
ENST00000706954.1:c.955_956delinsCT	ENSP00000516674.1:p.Thr319Leu
ENST00000706955.1:c.*990_*991delinsCT	ENSP00000516675.1:n.*990_*991delinsCT
ENST00000686459.1:c.*541_*542delinsCT	ENSP00000508909.1:n.*541_*542delinsCT
ENST00000688158.1:c.*1066_*1067delinsCT	ENSP00000509254.1:n.*1066_*1067delinsCT
ENST00000688308.1:c.955_956delinsCT	ENSP00000508752.1:p.Thr319Leu
ENST00000688922.1:c.876_877delinsCT
ENST00000693560.1:c.1474_1475delinsCT	ENSP00000509861.1:p.Thr492Leu
ENST00000371953.8:c.955_956delinsCT MANE Select	ENSP00000361021.3:p.Thr319Leu
ENST00000371953.7:c.955_956delinsCT	ENSP00000361021.3:p.Thr319Leu
ENST00000472832.2:c.382_383delinsCT	ENSP00000483066.1:p.Thr128Leu
NM_000314.5:c.955_956delinsCT	NP_000305.3:p.Thr319Leu
NM_000314.6:c.955_956delinsCT	NP_000305.3:p.Thr319Leu
NM_001304717.2:c.1474_1475delinsCT	NP_001291646.2:p.Thr492Leu
NM_001304718.1:c.364_365delinsCT	NP_001291647.1:p.Thr122Leu
XM_006717926.2:c.910_911delinsCT	XP_006717989.1:p.Thr304Leu
XM_011539981.1:c.955_956delinsCT	XP_011538283.1:p.Thr319Leu
XM_011539982.1:c.859_860delinsCT	XP_011538284.1:p.Thr287Leu
XR_945791.1:n.1525_1526delinsCT
NM_000314.7:c.955_956delinsCT	NP_000305.3:p.Thr319Leu
NM_001304717.5:c.1474_1475delinsCT	NP_001291646.4:p.Thr492Leu
NM_001304718.2:c.364_365delinsCT	NP_001291647.1:p.Thr122Leu
NM_000314.8:c.955_956delinsCT MANE Select	NP_000305.3:p.Thr319Leu