Canonical Allele Identifier: CA1926189998

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960963_87960964delinsGA , CM000672.2:g.87960963_87960964delinsGA	GRCh38
NC_000010.10:g.89720720_89720721delinsGA , CM000672.1:g.89720720_89720721delinsGA	GRCh37
NC_000010.9:g.89710700_89710701delinsGA	NCBI36
NG_007466.2:g.102525_102526delinsGA , LRG_311:g.102525_102526delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.964_965delinsGA	ENSP00000514759.2:p.Glu322=
ENST00000710265.1:c.871_872delinsGA	ENSP00000518161.1:p.Glu291=
ENST00000472832.3:c.871_872delinsGA	ENSP00000483066.2:p.Glu291=
ENST00000688158.2:n.1606_1607delinsGA
ENST00000688922.2:c.*701_*702delinsGA	ENSP00000508742.2:n.*701_*702delinsGA
ENST00000700021.1:c.826_827delinsGA	ENSP00000514757.1:p.Glu276=
ENST00000700022.1:c.*210_*211delinsGA	ENSP00000514758.1:n.*210_*211delinsGA
ENST00000700023.1:n.2029_2030delinsGA
ENST00000700024.1:n.2263_2264delinsGA
ENST00000700025.1:n.1640_1641delinsGA
ENST00000700026.1:n.508_509delinsGA
ENST00000700029.1:c.798_799delinsGA
ENST00000706954.1:c.871_872delinsGA	ENSP00000516674.1:p.Glu291=
ENST00000706955.1:c.*906_*907delinsGA	ENSP00000516675.1:n.*906_*907delinsGA
ENST00000686459.1:c.*457_*458delinsGA	ENSP00000508909.1:n.*457_*458delinsGA
ENST00000688158.1:c.*982_*983delinsGA	ENSP00000509254.1:n.*982_*983delinsGA
ENST00000688308.1:c.871_872delinsGA	ENSP00000508752.1:p.Glu291=
ENST00000688922.1:c.792_793delinsGA
ENST00000693560.1:c.1390_1391delinsGA	ENSP00000509861.1:p.Glu464=
ENST00000371953.8:c.871_872delinsGA MANE Select	ENSP00000361021.3:p.Glu291=
ENST00000371953.7:c.871_872delinsGA	ENSP00000361021.3:p.Glu291=
ENST00000472832.2:c.298_299delinsGA	ENSP00000483066.1:p.Glu100=
NM_000314.5:c.871_872delinsGA	NP_000305.3:p.Glu291=
NM_000314.6:c.871_872delinsGA	NP_000305.3:p.Glu291=
NM_001304717.2:c.1390_1391delinsGA	NP_001291646.2:p.Glu464=
NM_001304718.1:c.280_281delinsGA	NP_001291647.1:p.Glu94=
XM_006717926.2:c.826_827delinsGA	XP_006717989.1:p.Glu276=
XM_011539981.1:c.871_872delinsGA	XP_011538283.1:p.Glu291=
XM_011539982.1:c.775_776delinsGA	XP_011538284.1:p.Glu259=
XR_945791.1:n.1441_1442delinsGA
NM_000314.7:c.871_872delinsGA	NP_000305.3:p.Glu291=
NM_001304717.5:c.1390_1391delinsGA	NP_001291646.4:p.Glu464=
NM_001304718.2:c.280_281delinsGA	NP_001291647.1:p.Glu94=
NM_000314.8:c.871_872delinsGA MANE Select	NP_000305.3:p.Glu291=