Canonical Allele Identifier: CA891836132

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961014_87961015delinsAT , CM000672.2:g.87961014_87961015delinsAT	GRCh38
NC_000010.10:g.89720771_89720772delinsAT , CM000672.1:g.89720771_89720772delinsAT	GRCh37
NC_000010.9:g.89710751_89710752delinsAT	NCBI36
NG_007466.2:g.102576_102577delinsAT , LRG_311:g.102576_102577delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1015_1016delinsAT	ENSP00000514759.2:p.Arg339Ile
ENST00000710265.1:c.922_923delinsAT	ENSP00000518161.1:p.Arg308Ile
ENST00000472832.3:c.922_923delinsAT	ENSP00000483066.2:p.Arg308Ile
ENST00000688158.2:n.1657_1658delinsAT
ENST00000688922.2:c.*752_*753delinsAT	ENSP00000508742.2:n.*752_*753delinsAT
ENST00000700021.1:c.877_878delinsAT	ENSP00000514757.1:p.Arg293Ile
ENST00000700022.1:c.*261_*262delinsAT	ENSP00000514758.1:n.*261_*262delinsAT
ENST00000700023.1:n.2080_2081delinsAT
ENST00000700024.1:n.2314_2315delinsAT
ENST00000700025.1:n.1691_1692delinsAT
ENST00000700026.1:n.559_560delinsAT
ENST00000706954.1:c.922_923delinsAT	ENSP00000516674.1:p.Arg308Ile
ENST00000706955.1:c.*957_*958delinsAT	ENSP00000516675.1:n.*957_*958delinsAT
ENST00000686459.1:c.*508_*509delinsAT	ENSP00000508909.1:n.*508_*509delinsAT
ENST00000688158.1:c.*1033_*1034delinsAT	ENSP00000509254.1:n.*1033_*1034delinsAT
ENST00000688308.1:c.922_923delinsAT	ENSP00000508752.1:p.Arg308Ile
ENST00000688922.1:c.843_844delinsAT
ENST00000693560.1:c.1441_1442delinsAT	ENSP00000509861.1:p.Arg481Ile
ENST00000371953.8:c.922_923delinsAT MANE Select	ENSP00000361021.3:p.Arg308Ile
ENST00000371953.7:c.922_923delinsAT	ENSP00000361021.3:p.Arg308Ile
ENST00000472832.2:c.349_350delinsAT	ENSP00000483066.1:p.Arg117Ile
NM_000314.5:c.922_923delinsAT	NP_000305.3:p.Arg308Ile
NM_000314.6:c.922_923delinsAT	NP_000305.3:p.Arg308Ile
NM_001304717.2:c.1441_1442delinsAT	NP_001291646.2:p.Arg481Ile
NM_001304718.1:c.331_332delinsAT	NP_001291647.1:p.Arg111Ile
XM_006717926.2:c.877_878delinsAT	XP_006717989.1:p.Arg293Ile
XM_011539981.1:c.922_923delinsAT	XP_011538283.1:p.Arg308Ile
XM_011539982.1:c.826_827delinsAT	XP_011538284.1:p.Arg276Ile
XR_945791.1:n.1492_1493delinsAT
NM_000314.7:c.922_923delinsAT	NP_000305.3:p.Arg308Ile
NM_001304717.5:c.1441_1442delinsAT	NP_001291646.4:p.Arg481Ile
NM_001304718.2:c.331_332delinsAT	NP_001291647.1:p.Arg111Ile
NM_000314.8:c.922_923delinsAT MANE Select	NP_000305.3:p.Arg308Ile