Canonical Allele Identifier: CA2578697234

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98926608del , CM000668.2:g.98926608del	GRCh38
NC_000006.11:g.99374484del , CM000668.1:g.99374484del	GRCh37
NC_000006.10:g.99481205del	NCBI36
NG_033903.1:g.26400del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.382del MANE Select	ENSP00000358247.1:p.Glu128AsnfsTer16
ENST00000229971.2:c.382del	ENSP00000229971.1:p.Glu128AsnfsTer16
ENST00000369244.6:c.382del	ENSP00000358247.1:p.Glu128AsnfsTer16
NM_001278716.1:c.382del	NP_001265645.1:p.Glu128AsnfsTer16
NM_012160.4:c.382del	NP_036292.2:p.Glu128AsnfsTer16
NR_103836.1:n.773del
NR_103837.1:n.773del
XM_005266930.1:c.382del	XP_005266987.1:p.Glu128AsnfsTer16
XM_011535748.1:c.382del	XP_011534050.1:p.Glu128AsnfsTer16
XM_005266930.3:c.382del	XP_005266987.1:p.Glu128AsnfsTer16
XM_011535748.3:c.382del	XP_011534050.1:p.Glu128AsnfsTer16
XM_017010726.1:c.382del	XP_016866215.1:p.Glu128AsnfsTer16
XM_017010727.2:c.382del	XP_016866216.1:p.Glu128AsnfsTer16
XM_017010728.1:c.-421del	XP_016866217.1:n.-421del
NM_001278716.2:c.382del MANE Select	NP_001265645.1:p.Glu128AsnfsTer16
NR_103836.2:n.713del
NR_103837.2:n.713del
NM_012160.5:c.382del	NP_036292.2:p.Glu128AsnfsTer16