Canonical Allele Identifier: CA2496074368

Gene: FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47839423T= , CM000664.2:g.47839423T=	GRCh38
NC_000002.11:g.48066562T= , CM000664.1:g.48066562T=	GRCh37
NC_000002.10:g.47920066T=	NCBI36
NG_008397.1:g.71253A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681999.1:n.315A=
ENST00000682451.1:n.287A=
ENST00000682975.1:n.333A=
ENST00000683894.1:c.186A=	ENSP00000507789.1:p.Leu62=
ENST00000684085.1:n.315A=
ENST00000684712.1:n.546A=
ENST00000403359.8:c.438A= MANE Select	ENSP00000384823.4:p.Leu146=
ENST00000316377.8:c.204A=	ENSP00000323822.5:p.Leu68=
ENST00000402508.5:c.186A=	ENSP00000385398.1:p.Leu62=
ENST00000403359.7:c.438A=	ENSP00000384823.3:p.Leu146=
ENST00000424163.2:c.186A=	ENSP00000392272.1:p.Leu62=
ENST00000480038.1:n.401A=
ENST00000492225.5:n.286A=
NM_001190274.1:c.438A=	NP_001177203.1:p.Leu146=
NM_025133.4:c.186A=	NP_079409.3:p.Leu62=
XM_005264572.3:c.438A=	XP_005264629.1:p.Leu146=
XM_005264573.3:c.438A=	XP_005264630.1:p.Leu146=
XM_005264572.5:c.438A=	XP_005264629.1:p.Leu146=
XM_005264573.5:c.438A=	XP_005264630.1:p.Leu146=
XM_017005015.1:c.438A=	XP_016860504.1:p.Leu146=
XM_017005016.2:c.186A=	XP_016860505.1:p.Leu62=
XM_017005017.1:c.186A=	XP_016860506.1:p.Leu62=
NM_001190274.2:c.438A= MANE Select	NP_001177203.1:p.Leu146=
NM_001374325.1:c.186A=	NP_001361254.1:p.Leu62=