Canonical Allele Identifier: CA2679757536

Gene: FBXL4

Linked Data

• gnomAD v4: 6-98874284-A-AGACAG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98874285_98874286insACAGG , CM000668.2:g.98874285_98874286insACAGG	GRCh38
NC_000006.11:g.99322161_99322162insACAGG , CM000668.1:g.99322161_99322162insACAGG	GRCh37
NC_000006.10:g.99428882_99428883insACAGG	NCBI36
NG_033903.1:g.78722_78723insCTGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1859_1860insCTGTC MANE Select	ENSP00000358247.1:p.Gln621CysfsTer11
ENST00000229971.2:c.1859_1860insCTGTC	ENSP00000229971.1:p.Gln621CysfsTer11
ENST00000369244.6:c.1859_1860insCTGTC	ENSP00000358247.1:p.Gln621CysfsTer11
NM_001278716.1:c.1859_1860insCTGTC	NP_001265645.1:p.Gln621CysfsTer11
NM_012160.4:c.1859_1860insCTGTC	NP_036292.2:p.Gln621CysfsTer11
NR_103836.1:n.1904_1905insCTGTC
XM_005266930.1:c.1787_1788insCTGTC	XP_005266987.1:p.Gln597CysfsTer11
XM_005266930.3:c.1787_1788insCTGTC	XP_005266987.1:p.Gln597CysfsTer11
XM_017010726.1:c.1859_1860insCTGTC	XP_016866215.1:p.Gln621CysfsTer11
XM_017010727.2:c.1787_1788insCTGTC	XP_016866216.1:p.Gln597CysfsTer11
XM_017010728.1:c.1133_1134insCTGTC	XP_016866217.1:p.Gln379CysfsTer11
NM_001278716.2:c.1859_1860insCTGTC MANE Select	NP_001265645.1:p.Gln621CysfsTer11
NR_103836.2:n.1844_1845insCTGTC
NM_012160.5:c.1859_1860insCTGTC	NP_036292.2:p.Gln621CysfsTer11