Canonical Allele Identifier: CA917816029

Gene: FBXL4

Linked Data

• dbSNP Id: rs1582358155

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875092_98875095del , CM000668.2:g.98875092_98875095del	GRCh38
NC_000006.11:g.99322968_99322971del , CM000668.1:g.99322968_99322971del	GRCh37
NC_000006.10:g.99429689_99429692del	NCBI36
NG_033903.1:g.77916_77919del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1702+324_1702+327del MANE Select	ENSP00000358247.1:n.1702+324_1702+327del
ENST00000229971.2:c.1702+324_1702+327del	ENSP00000229971.1:n.1702+324_1702+327del
ENST00000369244.6:c.1702+324_1702+327del	ENSP00000358247.1:n.1702+324_1702+327del
NM_001278716.1:c.1702+324_1702+327del	NP_001265645.1:n.1702+324_1702+327del
NM_012160.4:c.1702+324_1702+327del	NP_036292.2:n.1702+324_1702+327del
NR_103836.1:n.1747+324_1747+327del
XM_005266930.1:c.1630+324_1630+327del	XP_005266987.1:n.1630+324_1630+327del
XM_005266930.3:c.1630+324_1630+327del	XP_005266987.1:n.1630+324_1630+327del
XM_017010726.1:c.1702+324_1702+327del	XP_016866215.1:n.1702+324_1702+327del
XM_017010727.2:c.1630+324_1630+327del	XP_016866216.1:n.1630+324_1630+327del
XM_017010728.1:c.976+324_976+327del	XP_016866217.1:n.976+324_976+327del
NM_001278716.2:c.1702+324_1702+327del MANE Select	NP_001265645.1:n.1702+324_1702+327del
NR_103836.2:n.1687+324_1687+327del
NM_012160.5:c.1702+324_1702+327del	NP_036292.2:n.1702+324_1702+327del