Canonical Allele Identifier: CA16020682

Gene: FBXL4

Linked Data

• ClinVar Variation Id: 437828
• ClinVar RCV Id: RCV000502890
• dbSNP Id: rs386704156

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98874273_98874275delinsCTG , CM000668.2:g.98874273_98874275delinsCTG	GRCh38
NC_000006.11:g.99322149_99322151delinsCTG , CM000668.1:g.99322149_99322151delinsCTG	GRCh37
NC_000006.10:g.99428870_99428872delinsCTG	NCBI36
NG_033903.1:g.78732_78734delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.*3_*5delinsCAG MANE Select	ENSP00000358247.1:n.*3_*5delinsCAG
ENST00000229971.2:c.*3_*5delinsCAG	ENSP00000229971.1:n.*3_*5delinsCAG
ENST00000369244.6:c.*3_*5delinsCAG	ENSP00000358247.1:n.*3_*5delinsCAG
NM_001278716.1:c.*3_*5delinsCAG	NP_001265645.1:n.*3_*5delinsCAG
NM_012160.4:c.*3_*5delinsCAG	NP_036292.2:n.*3_*5delinsCAG
NR_103836.1:n.1914_1916delinsCAG
XM_005266930.1:c.*3_*5delinsCAG	XP_005266987.1:n.*3_*5delinsCAG
XM_005266930.3:c.*3_*5delinsCAG	XP_005266987.1:n.*3_*5delinsCAG
XM_017010726.1:c.*3_*5delinsCAG	XP_016866215.1:n.*3_*5delinsCAG
XM_017010727.2:c.*3_*5delinsCAG	XP_016866216.1:n.*3_*5delinsCAG
XM_017010728.1:c.*3_*5delinsCAG	XP_016866217.1:n.*3_*5delinsCAG
NM_001278716.2:c.*3_*5delinsCAG MANE Select	NP_001265645.1:n.*3_*5delinsCAG
NR_103836.2:n.1854_1856delinsCAG
NM_012160.5:c.*3_*5delinsCAG	NP_036292.2:n.*3_*5delinsCAG