Canonical Allele Identifier: CA2772313726

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875526_98875612del , CM000668.2:g.98875526_98875612del	GRCh38
NC_000006.11:g.99323402_99323488del , CM000668.1:g.99323402_99323488del	GRCh37
NC_000006.10:g.99430123_99430209del	NCBI36
NG_033903.1:g.77395_77481del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1505_1591del MANE Select	ENSP00000358247.1:p.Ser502Ter
ENST00000229971.2:c.1505_1591del	ENSP00000229971.1:p.Ser502Ter
ENST00000369244.6:c.1505_1591del	ENSP00000358247.1:p.Ser502Ter
NM_001278716.1:c.1505_1591del	NP_001265645.1:p.Ser502Ter
NM_012160.4:c.1505_1591del	NP_036292.2:p.Ser502Ter
NR_103836.1:n.1550_1636del
XM_005266930.1:c.1433_1519del	XP_005266987.1:p.Ser478Ter
XM_005266930.3:c.1433_1519del	XP_005266987.1:p.Ser478Ter
XM_017010726.1:c.1505_1591del	XP_016866215.1:p.Ser502Ter
XM_017010727.2:c.1433_1519del	XP_016866216.1:p.Ser478Ter
XM_017010728.1:c.779_865del	XP_016866217.1:p.Ser260Ter
NM_001278716.2:c.1505_1591del MANE Select	NP_001265645.1:p.Ser502Ter
NR_103836.2:n.1490_1576del
NM_012160.5:c.1505_1591del	NP_036292.2:p.Ser502Ter