Canonical Allele Identifier: CA1649862565

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875296_98875297delinsTA , CM000668.2:g.98875296_98875297delinsTA	GRCh38
NC_000006.11:g.99323172_99323173delinsTA , CM000668.1:g.99323172_99323173delinsTA	GRCh37
NC_000006.10:g.99429893_99429894delinsTA	NCBI36
NG_033903.1:g.77710_77711delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1702+118_1702+119delinsTA MANE Select	ENSP00000358247.1:n.1702+118_1702+119delinsTA
ENST00000229971.2:c.1702+118_1702+119delinsTA	ENSP00000229971.1:n.1702+118_1702+119delinsTA
ENST00000369244.6:c.1702+118_1702+119delinsTA	ENSP00000358247.1:n.1702+118_1702+119delinsTA
NM_001278716.1:c.1702+118_1702+119delinsTA	NP_001265645.1:n.1702+118_1702+119delinsTA
NM_012160.4:c.1702+118_1702+119delinsTA	NP_036292.2:n.1702+118_1702+119delinsTA
NR_103836.1:n.1747+118_1747+119delinsTA
XM_005266930.1:c.1630+118_1630+119delinsTA	XP_005266987.1:n.1630+118_1630+119delinsTA
XM_005266930.3:c.1630+118_1630+119delinsTA	XP_005266987.1:n.1630+118_1630+119delinsTA
XM_017010726.1:c.1702+118_1702+119delinsTA	XP_016866215.1:n.1702+118_1702+119delinsTA
XM_017010727.2:c.1630+118_1630+119delinsTA	XP_016866216.1:n.1630+118_1630+119delinsTA
XM_017010728.1:c.976+118_976+119delinsTA	XP_016866217.1:n.976+118_976+119delinsTA
NM_001278716.2:c.1702+118_1702+119delinsTA MANE Select	NP_001265645.1:n.1702+118_1702+119delinsTA
NR_103836.2:n.1687+118_1687+119delinsTA
NM_012160.5:c.1702+118_1702+119delinsTA	NP_036292.2:n.1702+118_1702+119delinsTA