Canonical Allele Identifier: CA1649863055
Gene: FBXL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98875574A= , CM000668.2:g.98875574A= GRCh38
NC_000006.11:g.99323450A= , CM000668.1:g.99323450A= GRCh37
NC_000006.10:g.99430171A= NCBI36
NG_033903.1:g.77433T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369244.7:c.1543T= MANE Select ENSP00000358247.1:p.Cys515=
ENST00000229971.2:c.1543T= ENSP00000229971.1:p.Cys515=
ENST00000369244.6:c.1543T= ENSP00000358247.1:p.Cys515=
NM_001278716.1:c.1543T= NP_001265645.1:p.Cys515=
NM_012160.4:c.1543T= NP_036292.2:p.Cys515=
NR_103836.1:n.1588T=
XM_005266930.1:c.1471T= XP_005266987.1:p.Cys491=
XM_005266930.3:c.1471T= XP_005266987.1:p.Cys491=
XM_017010726.1:c.1543T= XP_016866215.1:p.Cys515=
XM_017010727.2:c.1471T= XP_016866216.1:p.Cys491=
XM_017010728.1:c.817T= XP_016866217.1:p.Cys273=
NM_001278716.2:c.1543T= MANE Select NP_001265645.1:p.Cys515=
NR_103836.2:n.1528T=
NM_012160.5:c.1543T= NP_036292.2:p.Cys515=