Canonical Allele Identifier: CA1649907143

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98926375_98926380delinsATTAAG , CM000668.2:g.98926375_98926380delinsATTAAG	GRCh38
NC_000006.11:g.99374251_99374256delinsATTAAG , CM000668.1:g.99374251_99374256delinsATTAAG	GRCh37
NC_000006.10:g.99480972_99480977delinsATTAAG	NCBI36
NG_033903.1:g.26627_26632delinsCTTAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.512+97_512+102delinsCTTAAT MANE Select	ENSP00000358247.1:n.512+97_512+102delinsCTTAAT
ENST00000229971.2:c.512+97_512+102delinsCTTAAT	ENSP00000229971.1:n.512+97_512+102delinsCTTAAT
ENST00000369244.6:c.512+97_512+102delinsCTTAAT	ENSP00000358247.1:n.512+97_512+102delinsCTTAAT
NM_001278716.1:c.512+97_512+102delinsCTTAAT	NP_001265645.1:n.512+97_512+102delinsCTTAAT
NM_012160.4:c.512+97_512+102delinsCTTAAT	NP_036292.2:n.512+97_512+102delinsCTTAAT
NR_103836.1:n.903+97_903+102delinsCTTAAT
NR_103837.1:n.903+97_903+102delinsCTTAAT
XM_005266930.1:c.512+97_512+102delinsCTTAAT	XP_005266987.1:n.512+97_512+102delinsCTTAAT
XM_011535748.1:c.512+97_512+102delinsCTTAAT	XP_011534050.1:n.512+97_512+102delinsCTTAAT
XM_005266930.3:c.512+97_512+102delinsCTTAAT	XP_005266987.1:n.512+97_512+102delinsCTTAAT
XM_011535748.3:c.512+97_512+102delinsCTTAAT	XP_011534050.1:n.512+97_512+102delinsCTTAAT
XM_017010726.1:c.512+97_512+102delinsCTTAAT	XP_016866215.1:n.512+97_512+102delinsCTTAAT
XM_017010727.2:c.512+97_512+102delinsCTTAAT	XP_016866216.1:n.512+97_512+102delinsCTTAAT
XM_017010728.1:c.-291+97_-291+102delinsCTTAAT	XP_016866217.1:n.-291+97_-291+102delinsCTTAAT
NM_001278716.2:c.512+97_512+102delinsCTTAAT MANE Select	NP_001265645.1:n.512+97_512+102delinsCTTAAT
NR_103836.2:n.843+97_843+102delinsCTTAAT
NR_103837.2:n.843+97_843+102delinsCTTAAT
NM_012160.5:c.512+97_512+102delinsCTTAAT	NP_036292.2:n.512+97_512+102delinsCTTAAT