Canonical Allele Identifier: CA365086205

Gene: FBXL4

Linked Data

• MyVariant Identifiers: chr6:g.99323298G>C (hg19) ; chr6:g.98875422G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875422G>C , CM000668.2:g.98875422G>C	GRCh38
NC_000006.11:g.99323298G>C , CM000668.1:g.99323298G>C	GRCh37
NC_000006.10:g.99430019G>C	NCBI36
NG_033903.1:g.77585C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1695C>G MANE Select	ENSP00000358247.1:p.Asp565Glu
ENST00000229971.2:c.1695C>G	ENSP00000229971.1:p.Asp565Glu
ENST00000369244.6:c.1695C>G	ENSP00000358247.1:p.Asp565Glu
NM_001278716.1:c.1695C>G	NP_001265645.1:p.Asp565Glu
NM_012160.4:c.1695C>G	NP_036292.2:p.Asp565Glu
NR_103836.1:n.1740C>G
XM_005266930.1:c.1623C>G	XP_005266987.1:p.Asp541Glu
XM_005266930.3:c.1623C>G	XP_005266987.1:p.Asp541Glu
XM_017010726.1:c.1695C>G	XP_016866215.1:p.Asp565Glu
XM_017010727.2:c.1623C>G	XP_016866216.1:p.Asp541Glu
XM_017010728.1:c.969C>G	XP_016866217.1:p.Asp323Glu
NM_001278716.2:c.1695C>G MANE Select	NP_001265645.1:p.Asp565Glu
NR_103836.2:n.1680C>G
NM_012160.5:c.1695C>G	NP_036292.2:p.Asp565Glu