Canonical Allele Identifier: CA144886

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98899282G>A , CM000668.2:g.98899282G>A	GRCh38
NC_000006.11:g.99347158G>A , CM000668.1:g.99347158G>A	GRCh37
NC_000006.10:g.99453879G>A	NCBI36
NG_033903.1:g.53725C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001278716.2:c.1303C>T MANE Select	NP_001265645.1:p.Arg435Ter
ENST00000369244.7:c.1303C>T MANE Select	ENSP00000358247.1:p.Arg435Ter
NM_001278716.1:c.1303C>T	NP_001265645.1:p.Arg435Ter
NM_012160.4:c.1303C>T	NP_036292.2:p.Arg435Ter
NM_012160.5:c.1303C>T	NP_036292.2:p.Arg435Ter
NR_103836.1:n.1348C>T
NR_103836.2:n.1288C>T
NR_103837.1:n.1348C>T
NR_103837.2:n.1288C>T
ENST00000229971.2:c.1303C>T	ENSP00000229971.1:p.Arg435Ter
ENST00000369244.6:c.1303C>T	ENSP00000358247.1:p.Arg435Ter
XM_005266930.1:c.1303C>T	XP_005266987.1:p.Arg435Ter
XM_005266930.3:c.1303C>T	XP_005266987.1:p.Arg435Ter
XM_017010726.1:c.1303C>T	XP_016866215.1:p.Arg435Ter
XM_017010727.2:c.1303C>T	XP_016866216.1:p.Arg435Ter
XM_017010728.1:c.577C>T	XP_016866217.1:p.Arg193Ter