Canonical Allele Identifier: CA2679759294

Gene: FBXL4

Linked Data

• gnomAD v4: 6-98926660-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98926661del , CM000668.2:g.98926661del	GRCh38
NC_000006.11:g.99374537del , CM000668.1:g.99374537del	GRCh37
NC_000006.10:g.99481258del	NCBI36
NG_033903.1:g.26346del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.328del MANE Select	ENSP00000358247.1:p.Ala110LeufsTer?
ENST00000229971.2:c.328del	ENSP00000229971.1:p.Ala110LeufsTer?
ENST00000369244.6:c.328del	ENSP00000358247.1:p.Ala110LeufsTer?
NM_001278716.1:c.328del	NP_001265645.1:p.Ala110LeufsTer?
NM_012160.4:c.328del	NP_036292.2:p.Ala110LeufsTer?
NR_103836.1:n.719del
NR_103837.1:n.719del
XM_005266930.1:c.328del	XP_005266987.1:p.Ala110LeufsTer?
XM_011535748.1:c.328del	XP_011534050.1:p.Ala110LeufsTer?
XM_005266930.3:c.328del	XP_005266987.1:p.Ala110LeufsTer?
XM_011535748.3:c.328del	XP_011534050.1:p.Ala110LeufsTer?
XM_017010726.1:c.328del	XP_016866215.1:p.Ala110LeufsTer?
XM_017010727.2:c.328del	XP_016866216.1:p.Ala110LeufsTer?
XM_017010728.1:c.-475del	XP_016866217.1:n.-475del
NM_001278716.2:c.328del MANE Select	NP_001265645.1:p.Ala110LeufsTer?
NR_103836.2:n.659del
NR_103837.2:n.659del
NM_012160.5:c.328del	NP_036292.2:p.Ala110LeufsTer?