Canonical Allele Identifier: CA1649862874
Gene: FBXL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98875455C= , CM000668.2:g.98875455C= GRCh38
NC_000006.11:g.99323331C= , CM000668.1:g.99323331C= GRCh37
NC_000006.10:g.99430052C= NCBI36
NG_033903.1:g.77552G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369244.7:c.1662G= MANE Select ENSP00000358247.1:p.Leu554=
ENST00000229971.2:c.1662G= ENSP00000229971.1:p.Leu554=
ENST00000369244.6:c.1662G= ENSP00000358247.1:p.Leu554=
NM_001278716.1:c.1662G= NP_001265645.1:p.Leu554=
NM_012160.4:c.1662G= NP_036292.2:p.Leu554=
NR_103836.1:n.1707G=
XM_005266930.1:c.1590G= XP_005266987.1:p.Leu530=
XM_005266930.3:c.1590G= XP_005266987.1:p.Leu530=
XM_017010726.1:c.1662G= XP_016866215.1:p.Leu554=
XM_017010727.2:c.1590G= XP_016866216.1:p.Leu530=
XM_017010728.1:c.936G= XP_016866217.1:p.Leu312=
NM_001278716.2:c.1662G= MANE Select NP_001265645.1:p.Leu554=
NR_103836.2:n.1647G=
NM_012160.5:c.1662G= NP_036292.2:p.Leu554=