Canonical Allele Identifier: CA1649860884

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98874249_98874250delinsAT , CM000668.2:g.98874249_98874250delinsAT	GRCh38
NC_000006.11:g.99322125_99322126delinsAT , CM000668.1:g.99322125_99322126delinsAT	GRCh37
NC_000006.10:g.99428846_99428847delinsAT	NCBI36
NG_033903.1:g.78757_78758delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.*28_*29delinsAT MANE Select	ENSP00000358247.1:n.*28_*29delinsAT
ENST00000229971.2:c.*28_*29delinsAT	ENSP00000229971.1:n.*28_*29delinsAT
ENST00000369244.6:c.*28_*29delinsAT	ENSP00000358247.1:n.*28_*29delinsAT
NM_001278716.1:c.*28_*29delinsAT	NP_001265645.1:n.*28_*29delinsAT
NM_012160.4:c.*28_*29delinsAT	NP_036292.2:n.*28_*29delinsAT
NR_103836.1:n.1939_1940delinsAT
XM_005266930.1:c.*28_*29delinsAT	XP_005266987.1:n.*28_*29delinsAT
XM_005266930.3:c.*28_*29delinsAT	XP_005266987.1:n.*28_*29delinsAT
XM_017010726.1:c.*28_*29delinsAT	XP_016866215.1:n.*28_*29delinsAT
XM_017010727.2:c.*28_*29delinsAT	XP_016866216.1:n.*28_*29delinsAT
XM_017010728.1:c.*28_*29delinsAT	XP_016866217.1:n.*28_*29delinsAT
NM_001278716.2:c.*28_*29delinsAT MANE Select	NP_001265645.1:n.*28_*29delinsAT
NR_103836.2:n.1879_1880delinsAT
NM_012160.5:c.*28_*29delinsAT	NP_036292.2:n.*28_*29delinsAT