Canonical Allele Identifier: CA891837916

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933165_87933167delinsAGA , CM000672.2:g.87933165_87933167delinsAGA	GRCh38
NC_000010.10:g.89692922_89692924delinsAGA , CM000672.1:g.89692922_89692924delinsAGA	GRCh37
NC_000010.9:g.89682902_89682904delinsAGA	NCBI36
NG_007466.2:g.74727_74729delinsAGA , LRG_311:g.74727_74729delinsAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.406_408delinsAGA	ENSP00000514759.2:p.Cys136Arg
ENST00000710265.1:c.406_408delinsAGA	ENSP00000518161.1:p.Cys136Arg
ENST00000472832.3:c.406_408delinsAGA	ENSP00000483066.2:p.Cys136Arg
ENST00000688158.2:n.1141_1143delinsAGA
ENST00000688922.2:c.*236_*238delinsAGA	ENSP00000508742.2:n.*236_*238delinsAGA
ENST00000700021.1:c.361_363delinsAGA	ENSP00000514757.1:p.Cys121Arg
ENST00000700022.1:c.406_408delinsAGA	ENSP00000514758.1:p.Cys136Arg
ENST00000700029.1:c.240_242delinsAGA
ENST00000706954.1:c.406_408delinsAGA	ENSP00000516674.1:p.Cys136Arg
ENST00000706955.1:c.*441_*443delinsAGA	ENSP00000516675.1:n.*441_*443delinsAGA
ENST00000686459.1:c.406_408delinsAGA	ENSP00000508909.1:p.Cys136Arg
ENST00000688158.1:c.*517_*519delinsAGA	ENSP00000509254.1:n.*517_*519delinsAGA
ENST00000688308.1:c.406_408delinsAGA	ENSP00000508752.1:p.Cys136Arg
ENST00000688922.1:c.327_329delinsAGA
ENST00000693560.1:c.925_927delinsAGA	ENSP00000509861.1:p.Cys309Arg
ENST00000371953.8:c.406_408delinsAGA MANE Select	ENSP00000361021.3:p.Cys136Arg
ENST00000371953.7:c.406_408delinsAGA	ENSP00000361021.3:p.Cys136Arg
ENST00000498703.1:n.232_234delinsAGA
ENST00000610634.1:c.304_306delinsAGA	ENSP00000477517.1:p.Cys102Arg
NM_000314.5:c.406_408delinsAGA	NP_000305.3:p.Cys136Arg
NM_000314.6:c.406_408delinsAGA	NP_000305.3:p.Cys136Arg
NM_001304717.2:c.925_927delinsAGA	NP_001291646.2:p.Cys309Arg
NM_001304718.1:c.-345_-343delinsAGA	NP_001291647.1:n.-345_-343delinsAGA
XM_006717926.2:c.361_363delinsAGA	XP_006717989.1:p.Cys121Arg
XM_011539981.1:c.406_408delinsAGA	XP_011538283.1:p.Cys136Arg
XM_011539982.1:c.310_312delinsAGA	XP_011538284.1:p.Cys104Arg
XR_945789.1:n.1118_1120delinsAGA
XR_945790.1:n.1118_1120delinsAGA
XR_945791.1:n.1118_1120delinsAGA
NM_000314.7:c.406_408delinsAGA	NP_000305.3:p.Cys136Arg
NM_001304717.5:c.925_927delinsAGA	NP_001291646.4:p.Cys309Arg
NM_001304718.2:c.-345_-343delinsAGA	NP_001291647.1:n.-345_-343delinsAGA
NM_000314.8:c.406_408delinsAGA MANE Select	NP_000305.3:p.Cys136Arg