Canonical Allele Identifier: CA365087160

Gene: FBXL4

Linked Data

• gnomAD v4: 6-98875585-T-A
• MyVariant Identifiers: chr6:g.99323461T>A (hg19) ; chr6:g.98875585T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875585T>A , CM000668.2:g.98875585T>A	GRCh38
NC_000006.11:g.99323461T>A , CM000668.1:g.99323461T>A	GRCh37
NC_000006.10:g.99430182T>A	NCBI36
NG_033903.1:g.77422A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1532A>T MANE Select	ENSP00000358247.1:p.Asp511Val
ENST00000229971.2:c.1532A>T	ENSP00000229971.1:p.Asp511Val
ENST00000369244.6:c.1532A>T	ENSP00000358247.1:p.Asp511Val
NM_001278716.1:c.1532A>T	NP_001265645.1:p.Asp511Val
NM_012160.4:c.1532A>T	NP_036292.2:p.Asp511Val
NR_103836.1:n.1577A>T
XM_005266930.1:c.1460A>T	XP_005266987.1:p.Asp487Val
XM_005266930.3:c.1460A>T	XP_005266987.1:p.Asp487Val
XM_017010726.1:c.1532A>T	XP_016866215.1:p.Asp511Val
XM_017010727.2:c.1460A>T	XP_016866216.1:p.Asp487Val
XM_017010728.1:c.806A>T	XP_016866217.1:p.Asp269Val
NM_001278716.2:c.1532A>T MANE Select	NP_001265645.1:p.Asp511Val
NR_103836.2:n.1517A>T
NM_012160.5:c.1532A>T	NP_036292.2:p.Asp511Val