Canonical Allele Identifier: CA2695203436

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960957_87960958insT , CM000672.2:g.87960957_87960958insT	GRCh38
NC_000010.10:g.89720714_89720715insT , CM000672.1:g.89720714_89720715insT	GRCh37
NC_000010.9:g.89710694_89710695insT	NCBI36
NG_007466.2:g.102519_102520insT , LRG_311:g.102519_102520insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.958_959insT	ENSP00000514759.2:p.Lys320IlefsTer9
ENST00000710265.1:c.865_866insT	ENSP00000518161.1:p.Lys289IlefsTer9
ENST00000472832.3:c.865_866insT	ENSP00000483066.2:p.Lys289IlefsTer9
ENST00000688158.2:n.1600_1601insT
ENST00000688922.2:c.*695_*696insT	ENSP00000508742.2:n.*695_*696insT
ENST00000700021.1:c.820_821insT	ENSP00000514757.1:p.Lys274IlefsTer9
ENST00000700022.1:c.*204_*205insT	ENSP00000514758.1:n.*204_*205insT
ENST00000700023.1:n.2023_2024insT
ENST00000700024.1:n.2257_2258insT
ENST00000700025.1:n.1634_1635insT
ENST00000700026.1:n.502_503insT
ENST00000700029.1:c.792_793insT
ENST00000706954.1:c.865_866insT	ENSP00000516674.1:p.Lys289IlefsTer9
ENST00000706955.1:c.*900_*901insT	ENSP00000516675.1:n.*900_*901insT
ENST00000686459.1:c.*451_*452insT	ENSP00000508909.1:n.*451_*452insT
ENST00000688158.1:c.*976_*977insT	ENSP00000509254.1:n.*976_*977insT
ENST00000688308.1:c.865_866insT	ENSP00000508752.1:p.Lys289IlefsTer9
ENST00000688922.1:c.786_787insT
ENST00000693560.1:c.1384_1385insT	ENSP00000509861.1:p.Lys462IlefsTer9
ENST00000371953.8:c.865_866insT MANE Select	ENSP00000361021.3:p.Lys289IlefsTer9
ENST00000371953.7:c.865_866insT	ENSP00000361021.3:p.Lys289IlefsTer9
ENST00000472832.2:c.292_293insT	ENSP00000483066.1:p.Lys98IlefsTer9
NM_000314.5:c.865_866insT	NP_000305.3:p.Lys289IlefsTer9
NM_000314.6:c.865_866insT	NP_000305.3:p.Lys289IlefsTer9
NM_001304717.2:c.1384_1385insT	NP_001291646.2:p.Lys462IlefsTer9
NM_001304718.1:c.274_275insT	NP_001291647.1:p.Lys92IlefsTer9
XM_006717926.2:c.820_821insT	XP_006717989.1:p.Lys274IlefsTer9
XM_011539981.1:c.865_866insT	XP_011538283.1:p.Lys289IlefsTer9
XM_011539982.1:c.769_770insT	XP_011538284.1:p.Lys257IlefsTer9
XR_945791.1:n.1435_1436insT
NM_000314.7:c.865_866insT	NP_000305.3:p.Lys289IlefsTer9
NM_001304717.5:c.1384_1385insT	NP_001291646.4:p.Lys462IlefsTer9
NM_001304718.2:c.274_275insT	NP_001291647.1:p.Lys92IlefsTer9
NM_000314.8:c.865_866insT MANE Select	NP_000305.3:p.Lys289IlefsTer9