Canonical Allele Identifier: CA1649863060
Gene: FBXL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98875577A= , CM000668.2:g.98875577A= GRCh38
NC_000006.11:g.99323453A= , CM000668.1:g.99323453A= GRCh37
NC_000006.10:g.99430174A= NCBI36
NG_033903.1:g.77430T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369244.7:c.1540T= MANE Select ENSP00000358247.1:p.Trp514=
ENST00000229971.2:c.1540T= ENSP00000229971.1:p.Trp514=
ENST00000369244.6:c.1540T= ENSP00000358247.1:p.Trp514=
NM_001278716.1:c.1540T= NP_001265645.1:p.Trp514=
NM_012160.4:c.1540T= NP_036292.2:p.Trp514=
NR_103836.1:n.1585T=
XM_005266930.1:c.1468T= XP_005266987.1:p.Trp490=
XM_005266930.3:c.1468T= XP_005266987.1:p.Trp490=
XM_017010726.1:c.1540T= XP_016866215.1:p.Trp514=
XM_017010727.2:c.1468T= XP_016866216.1:p.Trp490=
XM_017010728.1:c.814T= XP_016866217.1:p.Trp272=
NM_001278716.2:c.1540T= MANE Select NP_001265645.1:p.Trp514=
NR_103836.2:n.1525T=
NM_012160.5:c.1540T= NP_036292.2:p.Trp514=