Canonical Allele Identifier: CA1649861576
Gene: FBXL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98874464A= , CM000668.2:g.98874464A= GRCh38
NC_000006.11:g.99322340A= , CM000668.1:g.99322340A= GRCh37
NC_000006.10:g.99429061A= NCBI36
NG_033903.1:g.78543T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369244.7:c.1703-23T= MANE Select ENSP00000358247.1:n.1703-23T=
ENST00000229971.2:c.1703-23T= ENSP00000229971.1:n.1703-23T=
ENST00000369244.6:c.1703-23T= ENSP00000358247.1:n.1703-23T=
NM_001278716.1:c.1703-23T= NP_001265645.1:n.1703-23T=
NM_012160.4:c.1703-23T= NP_036292.2:n.1703-23T=
NR_103836.1:n.1748-23T=
XM_005266930.1:c.1631-23T= XP_005266987.1:n.1631-23T=
XM_005266930.3:c.1631-23T= XP_005266987.1:n.1631-23T=
XM_017010726.1:c.1703-23T= XP_016866215.1:n.1703-23T=
XM_017010727.2:c.1631-23T= XP_016866216.1:n.1631-23T=
XM_017010728.1:c.977-23T= XP_016866217.1:n.977-23T=
NM_001278716.2:c.1703-23T= MANE Select NP_001265645.1:n.1703-23T=
NR_103836.2:n.1688-23T=
NM_012160.5:c.1703-23T= NP_036292.2:n.1703-23T=