Canonical Allele Identifier: CA2510902254

Gene: FBXO11

Linked Data

• ClinVar Variation Id: 2756341
• ClinVar RCV Id: RCV003571733

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47839416T>C , CM000664.2:g.47839416T>C	GRCh38
NC_000002.11:g.48066555T>C , CM000664.1:g.48066555T>C	GRCh37
NC_000002.10:g.47920059T>C	NCBI36
NG_008397.1:g.71260A>G

Transcript Alleles

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