Canonical Allele Identifier: CA891836549

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961047_87961048delinsTT , CM000672.2:g.87961047_87961048delinsTT	GRCh38
NC_000010.10:g.89720804_89720805delinsTT , CM000672.1:g.89720804_89720805delinsTT	GRCh37
NC_000010.9:g.89710784_89710785delinsTT	NCBI36
NG_007466.2:g.102609_102610delinsTT , LRG_311:g.102609_102610delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1048_1049delinsTT	ENSP00000514759.2:p.Thr350Phe
ENST00000710265.1:c.955_956delinsTT	ENSP00000518161.1:p.Thr319Phe
ENST00000472832.3:c.955_956delinsTT	ENSP00000483066.2:p.Thr319Phe
ENST00000688158.2:n.1690_1691delinsTT
ENST00000688922.2:c.*785_*786delinsTT	ENSP00000508742.2:n.*785_*786delinsTT
ENST00000700021.1:c.910_911delinsTT	ENSP00000514757.1:p.Thr304Phe
ENST00000700022.1:c.*294_*295delinsTT	ENSP00000514758.1:n.*294_*295delinsTT
ENST00000700023.1:n.2113_2114delinsTT
ENST00000700024.1:n.2347_2348delinsTT
ENST00000700025.1:n.1724_1725delinsTT
ENST00000700026.1:n.592_593delinsTT
ENST00000706954.1:c.955_956delinsTT	ENSP00000516674.1:p.Thr319Phe
ENST00000706955.1:c.*990_*991delinsTT	ENSP00000516675.1:n.*990_*991delinsTT
ENST00000686459.1:c.*541_*542delinsTT	ENSP00000508909.1:n.*541_*542delinsTT
ENST00000688158.1:c.*1066_*1067delinsTT	ENSP00000509254.1:n.*1066_*1067delinsTT
ENST00000688308.1:c.955_956delinsTT	ENSP00000508752.1:p.Thr319Phe
ENST00000688922.1:c.876_877delinsTT
ENST00000693560.1:c.1474_1475delinsTT	ENSP00000509861.1:p.Thr492Phe
ENST00000371953.8:c.955_956delinsTT MANE Select	ENSP00000361021.3:p.Thr319Phe
ENST00000371953.7:c.955_956delinsTT	ENSP00000361021.3:p.Thr319Phe
ENST00000472832.2:c.382_383delinsTT	ENSP00000483066.1:p.Thr128Phe
NM_000314.5:c.955_956delinsTT	NP_000305.3:p.Thr319Phe
NM_000314.6:c.955_956delinsTT	NP_000305.3:p.Thr319Phe
NM_001304717.2:c.1474_1475delinsTT	NP_001291646.2:p.Thr492Phe
NM_001304718.1:c.364_365delinsTT	NP_001291647.1:p.Thr122Phe
XM_006717926.2:c.910_911delinsTT	XP_006717989.1:p.Thr304Phe
XM_011539981.1:c.955_956delinsTT	XP_011538283.1:p.Thr319Phe
XM_011539982.1:c.859_860delinsTT	XP_011538284.1:p.Thr287Phe
XR_945791.1:n.1525_1526delinsTT
NM_000314.7:c.955_956delinsTT	NP_000305.3:p.Thr319Phe
NM_001304717.5:c.1474_1475delinsTT	NP_001291646.4:p.Thr492Phe
NM_001304718.2:c.364_365delinsTT	NP_001291647.1:p.Thr122Phe
NM_000314.8:c.955_956delinsTT MANE Select	NP_000305.3:p.Thr319Phe