Canonical Allele Identifier: CA891841102

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960954_87960955delinsAT , CM000672.2:g.87960954_87960955delinsAT	GRCh38
NC_000010.10:g.89720711_89720712delinsAT , CM000672.1:g.89720711_89720712delinsAT	GRCh37
NC_000010.9:g.89710691_89710692delinsAT	NCBI36
NG_007466.2:g.102516_102517delinsAT , LRG_311:g.102516_102517delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.955_956delinsAT	ENSP00000514759.2:p.Glu319Ile
ENST00000710265.1:c.862_863delinsAT	ENSP00000518161.1:p.Glu288Ile
ENST00000472832.3:c.862_863delinsAT	ENSP00000483066.2:p.Glu288Ile
ENST00000688158.2:n.1597_1598delinsAT
ENST00000688922.2:c.*692_*693delinsAT	ENSP00000508742.2:n.*692_*693delinsAT
ENST00000700021.1:c.817_818delinsAT	ENSP00000514757.1:p.Glu273Ile
ENST00000700022.1:c.*201_*202delinsAT	ENSP00000514758.1:n.*201_*202delinsAT
ENST00000700023.1:n.2020_2021delinsAT
ENST00000700024.1:n.2254_2255delinsAT
ENST00000700025.1:n.1631_1632delinsAT
ENST00000700026.1:n.499_500delinsAT
ENST00000700029.1:c.789_790delinsAT
ENST00000706954.1:c.862_863delinsAT	ENSP00000516674.1:p.Glu288Ile
ENST00000706955.1:c.*897_*898delinsAT	ENSP00000516675.1:n.*897_*898delinsAT
ENST00000686459.1:c.*448_*449delinsAT	ENSP00000508909.1:n.*448_*449delinsAT
ENST00000688158.1:c.*973_*974delinsAT	ENSP00000509254.1:n.*973_*974delinsAT
ENST00000688308.1:c.862_863delinsAT	ENSP00000508752.1:p.Glu288Ile
ENST00000688922.1:c.783_784delinsAT
ENST00000693560.1:c.1381_1382delinsAT	ENSP00000509861.1:p.Glu461Ile
ENST00000371953.8:c.862_863delinsAT MANE Select	ENSP00000361021.3:p.Glu288Ile
ENST00000371953.7:c.862_863delinsAT	ENSP00000361021.3:p.Glu288Ile
ENST00000472832.2:c.289_290delinsAT	ENSP00000483066.1:p.Glu97Ile
NM_000314.5:c.862_863delinsAT	NP_000305.3:p.Glu288Ile
NM_000314.6:c.862_863delinsAT	NP_000305.3:p.Glu288Ile
NM_001304717.2:c.1381_1382delinsAT	NP_001291646.2:p.Glu461Ile
NM_001304718.1:c.271_272delinsAT	NP_001291647.1:p.Glu91Ile
XM_006717926.2:c.817_818delinsAT	XP_006717989.1:p.Glu273Ile
XM_011539981.1:c.862_863delinsAT	XP_011538283.1:p.Glu288Ile
XM_011539982.1:c.766_767delinsAT	XP_011538284.1:p.Glu256Ile
XR_945791.1:n.1432_1433delinsAT
NM_000314.7:c.862_863delinsAT	NP_000305.3:p.Glu288Ile
NM_001304717.5:c.1381_1382delinsAT	NP_001291646.4:p.Glu461Ile
NM_001304718.2:c.271_272delinsAT	NP_001291647.1:p.Glu91Ile
NM_000314.8:c.862_863delinsAT MANE Select	NP_000305.3:p.Glu288Ile