Canonical Allele Identifier: CA3933674

Gene: FBXL4

Linked Data

• dbSNP Id: rs774574475
• ExAC: 6:99374303 AC / A
• gnomAD v2: 6-99374303-AC-A
• gnomAD v3: 6-98926427-AC-A
• gnomAD v4: 6-98926427-AC-A
• MyVariant Identifiers: chr6:g.99374304del (hg19) ; chr6:g.98926428del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98926429del , CM000668.2:g.98926429del	GRCh38
NC_000006.11:g.99374305del , CM000668.1:g.99374305del	GRCh37
NC_000006.10:g.99481026del	NCBI36
NG_033903.1:g.26579del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.512+49del MANE Select	ENSP00000358247.1:n.512+49del
ENST00000229971.2:c.512+49del	ENSP00000229971.1:n.512+49del
ENST00000369244.6:c.512+49del	ENSP00000358247.1:n.512+49del
NM_001278716.1:c.512+49del	NP_001265645.1:n.512+49del
NM_012160.4:c.512+49del	NP_036292.2:n.512+49del
NR_103836.1:n.903+49del
NR_103837.1:n.903+49del
XM_005266930.1:c.512+49del	XP_005266987.1:n.512+49del
XM_011535748.1:c.512+49del	XP_011534050.1:n.512+49del
XM_005266930.3:c.512+49del	XP_005266987.1:n.512+49del
XM_011535748.3:c.512+49del	XP_011534050.1:n.512+49del
XM_017010726.1:c.512+49del	XP_016866215.1:n.512+49del
XM_017010727.2:c.512+49del	XP_016866216.1:n.512+49del
XM_017010728.1:c.-291+49del	XP_016866217.1:n.-291+49del
NM_001278716.2:c.512+49del MANE Select	NP_001265645.1:n.512+49del
NR_103836.2:n.843+49del
NR_103837.2:n.843+49del
NM_012160.5:c.512+49del	NP_036292.2:n.512+49del