Canonical Allele Identifier: CA1649860979

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98874282T= , CM000668.2:g.98874282T=	GRCh38
NC_000006.11:g.99322158T= , CM000668.1:g.99322158T=	GRCh37
NC_000006.10:g.99428879T=	NCBI36
NG_033903.1:g.78725A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1862A= MANE Select	ENSP00000358247.1:p.Gln621=
ENST00000229971.2:c.1862A=	ENSP00000229971.1:p.Gln621=
ENST00000369244.6:c.1862A=	ENSP00000358247.1:p.Gln621=
NM_001278716.1:c.1862A=	NP_001265645.1:p.Gln621=
NM_012160.4:c.1862A=	NP_036292.2:p.Gln621=
NR_103836.1:n.1907A=
XM_005266930.1:c.1790A=	XP_005266987.1:p.Gln597=
XM_005266930.3:c.1790A=	XP_005266987.1:p.Gln597=
XM_017010726.1:c.1862A=	XP_016866215.1:p.Gln621=
XM_017010727.2:c.1790A=	XP_016866216.1:p.Gln597=
XM_017010728.1:c.1136A=	XP_016866217.1:p.Gln379=
NM_001278716.2:c.1862A= MANE Select	NP_001265645.1:p.Gln621=
NR_103836.2:n.1847A=
NM_012160.5:c.1862A=	NP_036292.2:p.Gln621=