Canonical Allele Identifier: CA891835121

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960954_87960955delinsCC , CM000672.2:g.87960954_87960955delinsCC	GRCh38
NC_000010.10:g.89720711_89720712delinsCC , CM000672.1:g.89720711_89720712delinsCC	GRCh37
NC_000010.9:g.89710691_89710692delinsCC	NCBI36
NG_007466.2:g.102516_102517delinsCC , LRG_311:g.102516_102517delinsCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.955_956delinsCC	ENSP00000514759.2:p.Glu319Pro
ENST00000710265.1:c.862_863delinsCC	ENSP00000518161.1:p.Glu288Pro
ENST00000472832.3:c.862_863delinsCC	ENSP00000483066.2:p.Glu288Pro
ENST00000688158.2:n.1597_1598delinsCC
ENST00000688922.2:c.*692_*693delinsCC	ENSP00000508742.2:n.*692_*693delinsCC
ENST00000700021.1:c.817_818delinsCC	ENSP00000514757.1:p.Glu273Pro
ENST00000700022.1:c.*201_*202delinsCC	ENSP00000514758.1:n.*201_*202delinsCC
ENST00000700023.1:n.2020_2021delinsCC
ENST00000700024.1:n.2254_2255delinsCC
ENST00000700025.1:n.1631_1632delinsCC
ENST00000700026.1:n.499_500delinsCC
ENST00000700029.1:c.789_790delinsCC
ENST00000706954.1:c.862_863delinsCC	ENSP00000516674.1:p.Glu288Pro
ENST00000706955.1:c.*897_*898delinsCC	ENSP00000516675.1:n.*897_*898delinsCC
ENST00000686459.1:c.*448_*449delinsCC	ENSP00000508909.1:n.*448_*449delinsCC
ENST00000688158.1:c.*973_*974delinsCC	ENSP00000509254.1:n.*973_*974delinsCC
ENST00000688308.1:c.862_863delinsCC	ENSP00000508752.1:p.Glu288Pro
ENST00000688922.1:c.783_784delinsCC
ENST00000693560.1:c.1381_1382delinsCC	ENSP00000509861.1:p.Glu461Pro
ENST00000371953.8:c.862_863delinsCC MANE Select	ENSP00000361021.3:p.Glu288Pro
ENST00000371953.7:c.862_863delinsCC	ENSP00000361021.3:p.Glu288Pro
ENST00000472832.2:c.289_290delinsCC	ENSP00000483066.1:p.Glu97Pro
NM_000314.5:c.862_863delinsCC	NP_000305.3:p.Glu288Pro
NM_000314.6:c.862_863delinsCC	NP_000305.3:p.Glu288Pro
NM_001304717.2:c.1381_1382delinsCC	NP_001291646.2:p.Glu461Pro
NM_001304718.1:c.271_272delinsCC	NP_001291647.1:p.Glu91Pro
XM_006717926.2:c.817_818delinsCC	XP_006717989.1:p.Glu273Pro
XM_011539981.1:c.862_863delinsCC	XP_011538283.1:p.Glu288Pro
XM_011539982.1:c.766_767delinsCC	XP_011538284.1:p.Glu256Pro
XR_945791.1:n.1432_1433delinsCC
NM_000314.7:c.862_863delinsCC	NP_000305.3:p.Glu288Pro
NM_001304717.5:c.1381_1382delinsCC	NP_001291646.4:p.Glu461Pro
NM_001304718.2:c.271_272delinsCC	NP_001291647.1:p.Glu91Pro
NM_000314.8:c.862_863delinsCC MANE Select	NP_000305.3:p.Glu288Pro