Canonical Allele Identifier: CA1649861004

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98874290_98874292delinsGCT , CM000668.2:g.98874290_98874292delinsGCT	GRCh38
NC_000006.11:g.99322166_99322168delinsGCT , CM000668.1:g.99322166_99322168delinsGCT	GRCh37
NC_000006.10:g.99428887_99428889delinsGCT	NCBI36
NG_033903.1:g.78715_78717delinsAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1852_1854delinsAGC MANE Select	ENSP00000358247.1:p.Ser618=
ENST00000229971.2:c.1852_1854delinsAGC	ENSP00000229971.1:p.Ser618=
ENST00000369244.6:c.1852_1854delinsAGC	ENSP00000358247.1:p.Ser618=
NM_001278716.1:c.1852_1854delinsAGC	NP_001265645.1:p.Ser618=
NM_012160.4:c.1852_1854delinsAGC	NP_036292.2:p.Ser618=
NR_103836.1:n.1897_1899delinsAGC
XM_005266930.1:c.1780_1782delinsAGC	XP_005266987.1:p.Ser594=
XM_005266930.3:c.1780_1782delinsAGC	XP_005266987.1:p.Ser594=
XM_017010726.1:c.1852_1854delinsAGC	XP_016866215.1:p.Ser618=
XM_017010727.2:c.1780_1782delinsAGC	XP_016866216.1:p.Ser594=
XM_017010728.1:c.1126_1128delinsAGC	XP_016866217.1:p.Ser376=
NM_001278716.2:c.1852_1854delinsAGC MANE Select	NP_001265645.1:p.Ser618=
NR_103836.2:n.1837_1839delinsAGC
NM_012160.5:c.1852_1854delinsAGC	NP_036292.2:p.Ser618=