Canonical Allele Identifier: CA891836454

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933036_87933038delinsAGA , CM000672.2:g.87933036_87933038delinsAGA	GRCh38
NC_000010.10:g.89692793_89692795delinsAGA , CM000672.1:g.89692793_89692795delinsAGA	GRCh37
NC_000010.9:g.89682773_89682775delinsAGA	NCBI36
NG_007466.2:g.74598_74600delinsAGA , LRG_311:g.74598_74600delinsAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.277_279delinsAGA	ENSP00000514759.2:p.His93Arg
ENST00000710265.1:c.277_279delinsAGA	ENSP00000518161.1:p.His93Arg
ENST00000472832.3:c.277_279delinsAGA	ENSP00000483066.2:p.His93Arg
ENST00000688158.2:n.1012_1014delinsAGA
ENST00000688922.2:c.*107_*109delinsAGA	ENSP00000508742.2:n.*107_*109delinsAGA
ENST00000700021.1:c.232_234delinsAGA	ENSP00000514757.1:p.His78Arg
ENST00000700022.1:c.277_279delinsAGA	ENSP00000514758.1:p.His93Arg
ENST00000700029.1:c.111_113delinsAGA
ENST00000706954.1:c.277_279delinsAGA	ENSP00000516674.1:p.His93Arg
ENST00000706955.1:c.*312_*314delinsAGA	ENSP00000516675.1:n.*312_*314delinsAGA
ENST00000686459.1:c.277_279delinsAGA	ENSP00000508909.1:p.His93Arg
ENST00000688158.1:c.*388_*390delinsAGA	ENSP00000509254.1:n.*388_*390delinsAGA
ENST00000688308.1:c.277_279delinsAGA	ENSP00000508752.1:p.His93Arg
ENST00000688922.1:c.198_200delinsAGA
ENST00000693560.1:c.796_798delinsAGA	ENSP00000509861.1:p.His266Arg
ENST00000371953.8:c.277_279delinsAGA MANE Select	ENSP00000361021.3:p.His93Arg
ENST00000371953.7:c.277_279delinsAGA	ENSP00000361021.3:p.His93Arg
ENST00000498703.1:n.103_105delinsAGA
ENST00000610634.1:c.175_177delinsAGA	ENSP00000477517.1:p.His59Arg
NM_000314.5:c.277_279delinsAGA	NP_000305.3:p.His93Arg
NM_000314.6:c.277_279delinsAGA	NP_000305.3:p.His93Arg
NM_001304717.2:c.796_798delinsAGA	NP_001291646.2:p.His266Arg
NM_001304718.1:c.-474_-472delinsAGA	NP_001291647.1:n.-474_-472delinsAGA
XM_006717926.2:c.232_234delinsAGA	XP_006717989.1:p.His78Arg
XM_011539981.1:c.277_279delinsAGA	XP_011538283.1:p.His93Arg
XM_011539982.1:c.181_183delinsAGA	XP_011538284.1:p.His61Arg
XR_945789.1:n.989_991delinsAGA
XR_945790.1:n.989_991delinsAGA
XR_945791.1:n.989_991delinsAGA
NM_000314.7:c.277_279delinsAGA	NP_000305.3:p.His93Arg
NM_001304717.5:c.796_798delinsAGA	NP_001291646.4:p.His266Arg
NM_001304718.2:c.-474_-472delinsAGA	NP_001291647.1:n.-474_-472delinsAGA
NM_000314.8:c.277_279delinsAGA MANE Select	NP_000305.3:p.His93Arg