Canonical Allele Identifier: CA346812639

Gene: FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47905572T>C , CM000664.2:g.47905572T>C	GRCh38
NC_000002.11:g.48132711T>C , CM000664.1:g.48132711T>C	GRCh37
NC_000002.10:g.47986215T>C	NCBI36
NG_008397.1:g.5104A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001190274.2:c.149A>G MANE Select	NP_001177203.1:p.Gln50Arg
ENST00000403359.8:c.149A>G MANE Select	ENSP00000384823.4:p.Gln50Arg
NM_001190274.1:c.149A>G	NP_001177203.1:p.Gln50Arg
ENST00000316377.8:c.-84A>G	ENSP00000323822.5:n.-84A>G
ENST00000403359.7:c.149A>G	ENSP00000384823.3:p.Gln50Arg
ENST00000683894.1:c.-104A>G	ENSP00000507789.1:n.-104A>G
XM_005264572.3:c.149A>G	XP_005264629.1:p.Gln50Arg
XM_005264572.5:c.149A>G	XP_005264629.1:p.Gln50Arg
XM_005264573.3:c.149A>G	XP_005264630.1:p.Gln50Arg
XM_005264573.5:c.149A>G	XP_005264630.1:p.Gln50Arg
XM_017005015.1:c.149A>G	XP_016860504.1:p.Gln50Arg