Canonical Allele Identifier: CA2580617313
Gene: FBXL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98875677_98875682delinsATTTTTC , CM000668.2:g.98875677_98875682delinsATTTTTC GRCh38
NC_000006.11:g.99323553_99323558delinsATTTTTC , CM000668.1:g.99323553_99323558delinsATTTTTC GRCh37
NC_000006.10:g.99430274_99430279delinsATTTTTC NCBI36
NG_033903.1:g.77325_77330delinsGAAAAAT

Transcript Alleles

HGVS Amino-acid Change
NM_001278716.2:c.1435_1440delinsGAAAAAT MANE Select NP_001265645.1:p.Lys479GlufsTer12
ENST00000369244.7:c.1435_1440delinsGAAAAAT MANE Select ENSP00000358247.1:p.Lys479GlufsTer12
NM_001278716.1:c.1435_1440delinsGAAAAAT NP_001265645.1:p.Lys479GlufsTer12
NM_012160.4:c.1435_1440delinsGAAAAAT NP_036292.2:p.Lys479GlufsTer12
NM_012160.5:c.1435_1440delinsGAAAAAT NP_036292.2:p.Lys479GlufsTer12
NR_103836.1:n.1480_1485delinsGAAAAAT
NR_103836.2:n.1420_1425delinsGAAAAAT
ENST00000229971.2:c.1435_1440delinsGAAAAAT ENSP00000229971.1:p.Lys479GlufsTer12
ENST00000369244.6:c.1435_1440delinsGAAAAAT ENSP00000358247.1:p.Lys479GlufsTer12
XM_005266930.1:c.1363_1368delinsGAAAAAT XP_005266987.1:p.Lys455GlufsTer12
XM_005266930.3:c.1363_1368delinsGAAAAAT XP_005266987.1:p.Lys455GlufsTer12
XM_017010726.1:c.1435_1440delinsGAAAAAT XP_016866215.1:p.Lys479GlufsTer12
XM_017010727.2:c.1363_1368delinsGAAAAAT XP_016866216.1:p.Lys455GlufsTer12
XM_017010728.1:c.709_714delinsGAAAAAT XP_016866217.1:p.Lys237GlufsTer12