Canonical Allele Identifier: CA2496074356

Gene: FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47839398T= , CM000664.2:g.47839398T=	GRCh38
NC_000002.11:g.48066537T= , CM000664.1:g.48066537T=	GRCh37
NC_000002.10:g.47920041T=	NCBI36
NG_008397.1:g.71278A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681999.1:n.319+21A=
ENST00000682451.1:n.291+21A=
ENST00000682975.1:n.337+21A=
ENST00000683894.1:c.190+21A=	ENSP00000507789.1:n.190+21A=
ENST00000684085.1:n.319+21A=
ENST00000684712.1:n.550+21A=
ENST00000403359.8:c.442+21A= MANE Select	ENSP00000384823.4:n.442+21A=
ENST00000316377.8:c.208+21A=	ENSP00000323822.5:n.208+21A=
ENST00000402508.5:c.190+21A=	ENSP00000385398.1:n.190+21A=
ENST00000403359.7:c.442+21A=	ENSP00000384823.3:n.442+21A=
ENST00000424163.2:c.190+21A=	ENSP00000392272.1:n.190+21A=
ENST00000480038.1:n.405+21A=
ENST00000492225.5:n.290+21A=
NM_001190274.1:c.442+21A=	NP_001177203.1:n.442+21A=
NM_025133.4:c.190+21A=	NP_079409.3:n.190+21A=
XM_005264572.3:c.442+21A=	XP_005264629.1:n.442+21A=
XM_005264573.3:c.442+21A=	XP_005264630.1:n.442+21A=
XM_005264572.5:c.442+21A=	XP_005264629.1:n.442+21A=
XM_005264573.5:c.442+21A=	XP_005264630.1:n.442+21A=
XM_017005015.1:c.442+21A=	XP_016860504.1:n.442+21A=
XM_017005016.2:c.190+21A=	XP_016860505.1:n.190+21A=
XM_017005017.1:c.190+21A=	XP_016860506.1:n.190+21A=
NM_001190274.2:c.442+21A= MANE Select	NP_001177203.1:n.442+21A=
NM_001374325.1:c.190+21A=	NP_001361254.1:n.190+21A=