Canonical Allele Identifier: CA891841101

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960954_87960955delinsAC , CM000672.2:g.87960954_87960955delinsAC	GRCh38
NC_000010.10:g.89720711_89720712delinsAC , CM000672.1:g.89720711_89720712delinsAC	GRCh37
NC_000010.9:g.89710691_89710692delinsAC	NCBI36
NG_007466.2:g.102516_102517delinsAC , LRG_311:g.102516_102517delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.955_956delinsAC	ENSP00000514759.2:p.Glu319Thr
ENST00000710265.1:c.862_863delinsAC	ENSP00000518161.1:p.Glu288Thr
ENST00000472832.3:c.862_863delinsAC	ENSP00000483066.2:p.Glu288Thr
ENST00000688158.2:n.1597_1598delinsAC
ENST00000688922.2:c.*692_*693delinsAC	ENSP00000508742.2:n.*692_*693delinsAC
ENST00000700021.1:c.817_818delinsAC	ENSP00000514757.1:p.Glu273Thr
ENST00000700022.1:c.*201_*202delinsAC	ENSP00000514758.1:n.*201_*202delinsAC
ENST00000700023.1:n.2020_2021delinsAC
ENST00000700024.1:n.2254_2255delinsAC
ENST00000700025.1:n.1631_1632delinsAC
ENST00000700026.1:n.499_500delinsAC
ENST00000700029.1:c.789_790delinsAC
ENST00000706954.1:c.862_863delinsAC	ENSP00000516674.1:p.Glu288Thr
ENST00000706955.1:c.*897_*898delinsAC	ENSP00000516675.1:n.*897_*898delinsAC
ENST00000686459.1:c.*448_*449delinsAC	ENSP00000508909.1:n.*448_*449delinsAC
ENST00000688158.1:c.*973_*974delinsAC	ENSP00000509254.1:n.*973_*974delinsAC
ENST00000688308.1:c.862_863delinsAC	ENSP00000508752.1:p.Glu288Thr
ENST00000688922.1:c.783_784delinsAC
ENST00000693560.1:c.1381_1382delinsAC	ENSP00000509861.1:p.Glu461Thr
ENST00000371953.8:c.862_863delinsAC MANE Select	ENSP00000361021.3:p.Glu288Thr
ENST00000371953.7:c.862_863delinsAC	ENSP00000361021.3:p.Glu288Thr
ENST00000472832.2:c.289_290delinsAC	ENSP00000483066.1:p.Glu97Thr
NM_000314.5:c.862_863delinsAC	NP_000305.3:p.Glu288Thr
NM_000314.6:c.862_863delinsAC	NP_000305.3:p.Glu288Thr
NM_001304717.2:c.1381_1382delinsAC	NP_001291646.2:p.Glu461Thr
NM_001304718.1:c.271_272delinsAC	NP_001291647.1:p.Glu91Thr
XM_006717926.2:c.817_818delinsAC	XP_006717989.1:p.Glu273Thr
XM_011539981.1:c.862_863delinsAC	XP_011538283.1:p.Glu288Thr
XM_011539982.1:c.766_767delinsAC	XP_011538284.1:p.Glu256Thr
XR_945791.1:n.1432_1433delinsAC
NM_000314.7:c.862_863delinsAC	NP_000305.3:p.Glu288Thr
NM_001304717.5:c.1381_1382delinsAC	NP_001291646.4:p.Glu461Thr
NM_001304718.2:c.271_272delinsAC	NP_001291647.1:p.Glu91Thr
NM_000314.8:c.862_863delinsAC MANE Select	NP_000305.3:p.Glu288Thr