Canonical Allele Identifier: CA1649861289

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98874386A= , CM000668.2:g.98874386A=	GRCh38
NC_000006.11:g.99322262A= , CM000668.1:g.99322262A=	GRCh37
NC_000006.10:g.99428983A=	NCBI36
NG_033903.1:g.78621T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1758T= MANE Select	ENSP00000358247.1:p.Asp586=
ENST00000229971.2:c.1758T=	ENSP00000229971.1:p.Asp586=
ENST00000369244.6:c.1758T=	ENSP00000358247.1:p.Asp586=
NM_001278716.1:c.1758T=	NP_001265645.1:p.Asp586=
NM_012160.4:c.1758T=	NP_036292.2:p.Asp586=
NR_103836.1:n.1803T=
XM_005266930.1:c.1686T=	XP_005266987.1:p.Asp562=
XM_005266930.3:c.1686T=	XP_005266987.1:p.Asp562=
XM_017010726.1:c.1758T=	XP_016866215.1:p.Asp586=
XM_017010727.2:c.1686T=	XP_016866216.1:p.Asp562=
XM_017010728.1:c.1032T=	XP_016866217.1:p.Asp344=
NM_001278716.2:c.1758T= MANE Select	NP_001265645.1:p.Asp586=
NR_103836.2:n.1743T=
NM_012160.5:c.1758T=	NP_036292.2:p.Asp586=