Canonical Allele Identifier: CA2772313737

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875648_98875659del , CM000668.2:g.98875648_98875659del	GRCh38
NC_000006.11:g.99323524_99323535del , CM000668.1:g.99323524_99323535del	GRCh37
NC_000006.10:g.99430245_99430256del	NCBI36
NG_033903.1:g.77349_77360del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1459_1470del MANE Select	ENSP00000358247.1:p.Trp487_Lys490del
ENST00000229971.2:c.1459_1470del	ENSP00000229971.1:p.Trp487_Lys490del
ENST00000369244.6:c.1459_1470del	ENSP00000358247.1:p.Trp487_Lys490del
NM_001278716.1:c.1459_1470del	NP_001265645.1:p.Trp487_Lys490del
NM_012160.4:c.1459_1470del	NP_036292.2:p.Trp487_Lys490del
NR_103836.1:n.1504_1515del
XM_005266930.1:c.1387_1398del	XP_005266987.1:p.Trp463_Lys466del
XM_005266930.3:c.1387_1398del	XP_005266987.1:p.Trp463_Lys466del
XM_017010726.1:c.1459_1470del	XP_016866215.1:p.Trp487_Lys490del
XM_017010727.2:c.1387_1398del	XP_016866216.1:p.Trp463_Lys466del
XM_017010728.1:c.733_744del	XP_016866217.1:p.Trp245_Lys248del
NM_001278716.2:c.1459_1470del MANE Select	NP_001265645.1:p.Trp487_Lys490del
NR_103836.2:n.1444_1455del
NM_012160.5:c.1459_1470del	NP_036292.2:p.Trp487_Lys490del