Canonical Allele Identifier: CA1649862819

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875435_98875444delinsAACCTGGTAC , CM000668.2:g.98875435_98875444delinsAACCTGGTAC	GRCh38
NC_000006.11:g.99323311_99323320delinsAACCTGGTAC , CM000668.1:g.99323311_99323320delinsAACCTGGTAC	GRCh37
NC_000006.10:g.99430032_99430041delinsAACCTGGTAC	NCBI36
NG_033903.1:g.77563_77572delinsGTACCAGGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1673_1682delinsGTACCAGGTT MANE Select	ENSP00000358247.1:p.Cys558=
ENST00000229971.2:c.1673_1682delinsGTACCAGGTT	ENSP00000229971.1:p.Cys558=
ENST00000369244.6:c.1673_1682delinsGTACCAGGTT	ENSP00000358247.1:p.Cys558=
NM_001278716.1:c.1673_1682delinsGTACCAGGTT	NP_001265645.1:p.Cys558=
NM_012160.4:c.1673_1682delinsGTACCAGGTT	NP_036292.2:p.Cys558=
NR_103836.1:n.1718_1727delinsGTACCAGGTT
XM_005266930.1:c.1601_1610delinsGTACCAGGTT	XP_005266987.1:p.Cys534=
XM_005266930.3:c.1601_1610delinsGTACCAGGTT	XP_005266987.1:p.Cys534=
XM_017010726.1:c.1673_1682delinsGTACCAGGTT	XP_016866215.1:p.Cys558=
XM_017010727.2:c.1601_1610delinsGTACCAGGTT	XP_016866216.1:p.Cys534=
XM_017010728.1:c.947_956delinsGTACCAGGTT	XP_016866217.1:p.Cys316=
NM_001278716.2:c.1673_1682delinsGTACCAGGTT MANE Select	NP_001265645.1:p.Cys558=
NR_103836.2:n.1658_1667delinsGTACCAGGTT
NM_012160.5:c.1673_1682delinsGTACCAGGTT	NP_036292.2:p.Cys558=