Canonical Allele Identifier: CA1926189992

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960954_87960955delinsGA , CM000672.2:g.87960954_87960955delinsGA	GRCh38
NC_000010.10:g.89720711_89720712delinsGA , CM000672.1:g.89720711_89720712delinsGA	GRCh37
NC_000010.9:g.89710691_89710692delinsGA	NCBI36
NG_007466.2:g.102516_102517delinsGA , LRG_311:g.102516_102517delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.955_956delinsGA	ENSP00000514759.2:p.Glu319=
ENST00000710265.1:c.862_863delinsGA	ENSP00000518161.1:p.Glu288=
ENST00000472832.3:c.862_863delinsGA	ENSP00000483066.2:p.Glu288=
ENST00000688158.2:n.1597_1598delinsGA
ENST00000688922.2:c.*692_*693delinsGA	ENSP00000508742.2:n.*692_*693delinsGA
ENST00000700021.1:c.817_818delinsGA	ENSP00000514757.1:p.Glu273=
ENST00000700022.1:c.*201_*202delinsGA	ENSP00000514758.1:n.*201_*202delinsGA
ENST00000700023.1:n.2020_2021delinsGA
ENST00000700024.1:n.2254_2255delinsGA
ENST00000700025.1:n.1631_1632delinsGA
ENST00000700026.1:n.499_500delinsGA
ENST00000700029.1:c.789_790delinsGA
ENST00000706954.1:c.862_863delinsGA	ENSP00000516674.1:p.Glu288=
ENST00000706955.1:c.*897_*898delinsGA	ENSP00000516675.1:n.*897_*898delinsGA
ENST00000686459.1:c.*448_*449delinsGA	ENSP00000508909.1:n.*448_*449delinsGA
ENST00000688158.1:c.*973_*974delinsGA	ENSP00000509254.1:n.*973_*974delinsGA
ENST00000688308.1:c.862_863delinsGA	ENSP00000508752.1:p.Glu288=
ENST00000688922.1:c.783_784delinsGA
ENST00000693560.1:c.1381_1382delinsGA	ENSP00000509861.1:p.Glu461=
ENST00000371953.8:c.862_863delinsGA MANE Select	ENSP00000361021.3:p.Glu288=
ENST00000371953.7:c.862_863delinsGA	ENSP00000361021.3:p.Glu288=
ENST00000472832.2:c.289_290delinsGA	ENSP00000483066.1:p.Glu97=
NM_000314.5:c.862_863delinsGA	NP_000305.3:p.Glu288=
NM_000314.6:c.862_863delinsGA	NP_000305.3:p.Glu288=
NM_001304717.2:c.1381_1382delinsGA	NP_001291646.2:p.Glu461=
NM_001304718.1:c.271_272delinsGA	NP_001291647.1:p.Glu91=
XM_006717926.2:c.817_818delinsGA	XP_006717989.1:p.Glu273=
XM_011539981.1:c.862_863delinsGA	XP_011538283.1:p.Glu288=
XM_011539982.1:c.766_767delinsGA	XP_011538284.1:p.Glu256=
XR_945791.1:n.1432_1433delinsGA
NM_000314.7:c.862_863delinsGA	NP_000305.3:p.Glu288=
NM_001304717.5:c.1381_1382delinsGA	NP_001291646.4:p.Glu461=
NM_001304718.2:c.271_272delinsGA	NP_001291647.1:p.Glu91=
NM_000314.8:c.862_863delinsGA MANE Select	NP_000305.3:p.Glu288=