Canonical Allele Identifier: CA1649862283

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875071_98875075delinsAATTC , CM000668.2:g.98875071_98875075delinsAATTC	GRCh38
NC_000006.11:g.99322947_99322951delinsAATTC , CM000668.1:g.99322947_99322951delinsAATTC	GRCh37
NC_000006.10:g.99429668_99429672delinsAATTC	NCBI36
NG_033903.1:g.77932_77936delinsGAATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1702+340_1702+344delinsGAATT MANE Select	ENSP00000358247.1:n.1702+340_1702+344delinsGAATT
ENST00000229971.2:c.1702+340_1702+344delinsGAATT	ENSP00000229971.1:n.1702+340_1702+344delinsGAATT
ENST00000369244.6:c.1702+340_1702+344delinsGAATT	ENSP00000358247.1:n.1702+340_1702+344delinsGAATT
NM_001278716.1:c.1702+340_1702+344delinsGAATT	NP_001265645.1:n.1702+340_1702+344delinsGAATT
NM_012160.4:c.1702+340_1702+344delinsGAATT	NP_036292.2:n.1702+340_1702+344delinsGAATT
NR_103836.1:n.1747+340_1747+344delinsGAATT
XM_005266930.1:c.1630+340_1630+344delinsGAATT	XP_005266987.1:n.1630+340_1630+344delinsGAATT
XM_005266930.3:c.1630+340_1630+344delinsGAATT	XP_005266987.1:n.1630+340_1630+344delinsGAATT
XM_017010726.1:c.1702+340_1702+344delinsGAATT	XP_016866215.1:n.1702+340_1702+344delinsGAATT
XM_017010727.2:c.1630+340_1630+344delinsGAATT	XP_016866216.1:n.1630+340_1630+344delinsGAATT
XM_017010728.1:c.976+340_976+344delinsGAATT	XP_016866217.1:n.976+340_976+344delinsGAATT
NM_001278716.2:c.1702+340_1702+344delinsGAATT MANE Select	NP_001265645.1:n.1702+340_1702+344delinsGAATT
NR_103836.2:n.1687+340_1687+344delinsGAATT
NM_012160.5:c.1702+340_1702+344delinsGAATT	NP_036292.2:n.1702+340_1702+344delinsGAATT