Canonical Allele Identifier: CA3933516

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98899450G>A , CM000668.2:g.98899450G>A	GRCh38
NC_000006.11:g.99347326G>A , CM000668.1:g.99347326G>A	GRCh37
NC_000006.10:g.99454047G>A	NCBI36
NG_033903.1:g.53557C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1135C>T MANE Select	ENSP00000358247.1:p.Arg379Cys
ENST00000229971.2:c.1135C>T	ENSP00000229971.1:p.Arg379Cys
ENST00000369244.6:c.1135C>T	ENSP00000358247.1:p.Arg379Cys
NM_001278716.1:c.1135C>T	NP_001265645.1:p.Arg379Cys
NM_012160.4:c.1135C>T	NP_036292.2:p.Arg379Cys
NR_103836.1:n.1180C>T
NR_103837.1:n.1180C>T
XM_005266930.1:c.1135C>T	XP_005266987.1:p.Arg379Cys
XM_005266930.3:c.1135C>T	XP_005266987.1:p.Arg379Cys
XM_017010726.1:c.1135C>T	XP_016866215.1:p.Arg379Cys
XM_017010727.2:c.1135C>T	XP_016866216.1:p.Arg379Cys
XM_017010728.1:c.409C>T	XP_016866217.1:p.Arg137Cys
NM_001278716.2:c.1135C>T MANE Select	NP_001265645.1:p.Arg379Cys
NR_103836.2:n.1120C>T
NR_103837.2:n.1120C>T
NM_012160.5:c.1135C>T	NP_036292.2:p.Arg379Cys