Canonical Allele Identifier: CA365087402

Gene: FBXL4

Linked Data

• MyVariant Identifiers: chr6:g.99323500G>A (hg19) ; chr6:g.98875624G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875624G>A , CM000668.2:g.98875624G>A	GRCh38
NC_000006.11:g.99323500G>A , CM000668.1:g.99323500G>A	GRCh37
NC_000006.10:g.99430221G>A	NCBI36
NG_033903.1:g.77383C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1493C>T MANE Select	ENSP00000358247.1:p.Ala498Val
ENST00000229971.2:c.1493C>T	ENSP00000229971.1:p.Ala498Val
ENST00000369244.6:c.1493C>T	ENSP00000358247.1:p.Ala498Val
NM_001278716.1:c.1493C>T	NP_001265645.1:p.Ala498Val
NM_012160.4:c.1493C>T	NP_036292.2:p.Ala498Val
NR_103836.1:n.1538C>T
XM_005266930.1:c.1421C>T	XP_005266987.1:p.Ala474Val
XM_005266930.3:c.1421C>T	XP_005266987.1:p.Ala474Val
XM_017010726.1:c.1493C>T	XP_016866215.1:p.Ala498Val
XM_017010727.2:c.1421C>T	XP_016866216.1:p.Ala474Val
XM_017010728.1:c.767C>T	XP_016866217.1:p.Ala256Val
NM_001278716.2:c.1493C>T MANE Select	NP_001265645.1:p.Ala498Val
NR_103836.2:n.1478C>T
NM_012160.5:c.1493C>T	NP_036292.2:p.Ala498Val