Canonical Allele Identifier: CA2578696945

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98874487_98874488del , CM000668.2:g.98874487_98874488del	GRCh38
NC_000006.11:g.99322363_99322364del , CM000668.1:g.99322363_99322364del	GRCh37
NC_000006.10:g.99429084_99429085del	NCBI36
NG_033903.1:g.78521_78522del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1703-45_1703-44del MANE Select	ENSP00000358247.1:n.1703-45_1703-44del
ENST00000229971.2:c.1703-45_1703-44del	ENSP00000229971.1:n.1703-45_1703-44del
ENST00000369244.6:c.1703-45_1703-44del	ENSP00000358247.1:n.1703-45_1703-44del
NM_001278716.1:c.1703-45_1703-44del	NP_001265645.1:n.1703-45_1703-44del
NM_012160.4:c.1703-45_1703-44del	NP_036292.2:n.1703-45_1703-44del
NR_103836.1:n.1748-45_1748-44del
XM_005266930.1:c.1631-45_1631-44del	XP_005266987.1:n.1631-45_1631-44del
XM_005266930.3:c.1631-45_1631-44del	XP_005266987.1:n.1631-45_1631-44del
XM_017010726.1:c.1703-45_1703-44del	XP_016866215.1:n.1703-45_1703-44del
XM_017010727.2:c.1631-45_1631-44del	XP_016866216.1:n.1631-45_1631-44del
XM_017010728.1:c.977-45_977-44del	XP_016866217.1:n.977-45_977-44del
NM_001278716.2:c.1703-45_1703-44del MANE Select	NP_001265645.1:n.1703-45_1703-44del
NR_103836.2:n.1688-45_1688-44del
NM_012160.5:c.1703-45_1703-44del	NP_036292.2:n.1703-45_1703-44del