Canonical Allele Identifier: CA2679757527

Gene: FBXL4

Linked Data

• gnomAD v4: 6-98874246-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98874246C>A , CM000668.2:g.98874246C>A	GRCh38
NC_000006.11:g.99322122C>A , CM000668.1:g.99322122C>A	GRCh37
NC_000006.10:g.99428843C>A	NCBI36
NG_033903.1:g.78761G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.*32G>T MANE Select	ENSP00000358247.1:n.*32G>T
ENST00000229971.2:c.*32G>T	ENSP00000229971.1:n.*32G>T
ENST00000369244.6:c.*32G>T	ENSP00000358247.1:n.*32G>T
NM_001278716.1:c.*32G>T	NP_001265645.1:n.*32G>T
NM_012160.4:c.*32G>T	NP_036292.2:n.*32G>T
NR_103836.1:n.1943G>T
XM_005266930.1:c.*32G>T	XP_005266987.1:n.*32G>T
XM_005266930.3:c.*32G>T	XP_005266987.1:n.*32G>T
XM_017010726.1:c.*32G>T	XP_016866215.1:n.*32G>T
XM_017010727.2:c.*32G>T	XP_016866216.1:n.*32G>T
XM_017010728.1:c.*32G>T	XP_016866217.1:n.*32G>T
NM_001278716.2:c.*32G>T MANE Select	NP_001265645.1:n.*32G>T
NR_103836.2:n.1883G>T
NM_012160.5:c.*32G>T	NP_036292.2:n.*32G>T