Canonical Allele Identifier: CA365086662

Gene: FBXL4

Linked Data

• dbSNP Id: rs990596769
• MyVariant Identifiers: chr6:g.99323377A>C (hg19) ; chr6:g.98875501A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875501A>C , CM000668.2:g.98875501A>C	GRCh38
NC_000006.11:g.99323377A>C , CM000668.1:g.99323377A>C	GRCh37
NC_000006.10:g.99430098A>C	NCBI36
NG_033903.1:g.77506T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1616T>G MANE Select	ENSP00000358247.1:p.Phe539Cys
ENST00000229971.2:c.1616T>G	ENSP00000229971.1:p.Phe539Cys
ENST00000369244.6:c.1616T>G	ENSP00000358247.1:p.Phe539Cys
NM_001278716.1:c.1616T>G	NP_001265645.1:p.Phe539Cys
NM_012160.4:c.1616T>G	NP_036292.2:p.Phe539Cys
NR_103836.1:n.1661T>G
XM_005266930.1:c.1544T>G	XP_005266987.1:p.Phe515Cys
XM_005266930.3:c.1544T>G	XP_005266987.1:p.Phe515Cys
XM_017010726.1:c.1616T>G	XP_016866215.1:p.Phe539Cys
XM_017010727.2:c.1544T>G	XP_016866216.1:p.Phe515Cys
XM_017010728.1:c.890T>G	XP_016866217.1:p.Phe297Cys
NM_001278716.2:c.1616T>G MANE Select	NP_001265645.1:p.Phe539Cys
NR_103836.2:n.1601T>G
NM_012160.5:c.1616T>G	NP_036292.2:p.Phe539Cys