Canonical Allele Identifier: CA346813359

Gene: FBXO11

Linked Data

• MyVariant Identifiers: chr2:g.48066580A>T (hg19) ; chr2:g.47839441A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47839441A>T , CM000664.2:g.47839441A>T	GRCh38
NC_000002.11:g.48066580A>T , CM000664.1:g.48066580A>T	GRCh37
NC_000002.10:g.47920084A>T	NCBI36
NG_008397.1:g.71235T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681999.1:n.297T>A
ENST00000682451.1:n.269T>A
ENST00000682975.1:n.315T>A
ENST00000683894.1:c.168T>A	ENSP00000507789.1:p.Ser56=
ENST00000684085.1:n.297T>A
ENST00000684712.1:n.528T>A
ENST00000403359.8:c.420T>A MANE Select	ENSP00000384823.4:p.Ser140=
ENST00000316377.8:c.188T>A	ENSP00000323822.5:p.Leu63Gln
ENST00000402508.5:c.168T>A	ENSP00000385398.1:p.Ser56=
ENST00000403359.7:c.420T>A	ENSP00000384823.3:p.Ser140=
ENST00000424163.2:c.168T>A	ENSP00000392272.1:p.Ser56=
ENST00000480038.1:n.383T>A
ENST00000492225.5:n.268T>A
NM_001190274.1:c.420T>A	NP_001177203.1:p.Ser140=
NM_025133.4:c.168T>A	NP_079409.3:p.Ser56=
XM_005264572.3:c.420T>A	XP_005264629.1:p.Ser140=
XM_005264573.3:c.420T>A	XP_005264630.1:p.Ser140=
XM_005264572.5:c.420T>A	XP_005264629.1:p.Ser140=
XM_005264573.5:c.420T>A	XP_005264630.1:p.Ser140=
XM_017005015.1:c.420T>A	XP_016860504.1:p.Ser140=
XM_017005016.2:c.168T>A	XP_016860505.1:p.Ser56=
XM_017005017.1:c.168T>A	XP_016860506.1:p.Ser56=
NM_001190274.2:c.420T>A MANE Select	NP_001177203.1:p.Ser140=
NM_001374325.1:c.168T>A	NP_001361254.1:p.Ser56=