Canonical Allele Identifier: CA1649862882

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875462T= , CM000668.2:g.98875462T=	GRCh38
NC_000006.11:g.99323338T= , CM000668.1:g.99323338T=	GRCh37
NC_000006.10:g.99430059T=	NCBI36
NG_033903.1:g.77545A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1655A= MANE Select	ENSP00000358247.1:p.Asp552=
ENST00000229971.2:c.1655A=	ENSP00000229971.1:p.Asp552=
ENST00000369244.6:c.1655A=	ENSP00000358247.1:p.Asp552=
NM_001278716.1:c.1655A=	NP_001265645.1:p.Asp552=
NM_012160.4:c.1655A=	NP_036292.2:p.Asp552=
NR_103836.1:n.1700A=
XM_005266930.1:c.1583A=	XP_005266987.1:p.Asp528=
XM_005266930.3:c.1583A=	XP_005266987.1:p.Asp528=
XM_017010726.1:c.1655A=	XP_016866215.1:p.Asp552=
XM_017010727.2:c.1583A=	XP_016866216.1:p.Asp528=
XM_017010728.1:c.929A=	XP_016866217.1:p.Asp310=
NM_001278716.2:c.1655A= MANE Select	NP_001265645.1:p.Asp552=
NR_103836.2:n.1640A=
NM_012160.5:c.1655A=	NP_036292.2:p.Asp552=