Canonical Allele Identifier: CA1649861039

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98874307_98874308delinsCT , CM000668.2:g.98874307_98874308delinsCT	GRCh38
NC_000006.11:g.99322183_99322184delinsCT , CM000668.1:g.99322183_99322184delinsCT	GRCh37
NC_000006.10:g.99428904_99428905delinsCT	NCBI36
NG_033903.1:g.78699_78700delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1836_1837delinsAG MANE Select	ENSP00000358247.1:p.Lys612=
ENST00000229971.2:c.1836_1837delinsAG	ENSP00000229971.1:p.Lys612=
ENST00000369244.6:c.1836_1837delinsAG	ENSP00000358247.1:p.Lys612=
NM_001278716.1:c.1836_1837delinsAG	NP_001265645.1:p.Lys612=
NM_012160.4:c.1836_1837delinsAG	NP_036292.2:p.Lys612=
NR_103836.1:n.1881_1882delinsAG
XM_005266930.1:c.1764_1765delinsAG	XP_005266987.1:p.Lys588=
XM_005266930.3:c.1764_1765delinsAG	XP_005266987.1:p.Lys588=
XM_017010726.1:c.1836_1837delinsAG	XP_016866215.1:p.Lys612=
XM_017010727.2:c.1764_1765delinsAG	XP_016866216.1:p.Lys588=
XM_017010728.1:c.1110_1111delinsAG	XP_016866217.1:p.Lys370=
NM_001278716.2:c.1836_1837delinsAG MANE Select	NP_001265645.1:p.Lys612=
NR_103836.2:n.1821_1822delinsAG
NM_012160.5:c.1836_1837delinsAG	NP_036292.2:p.Lys612=