Canonical Allele Identifier: CA569080377

Gene: FBXL4

Linked Data

• dbSNP Id: rs1422335783
• gnomAD v2: 6-99322938-AC-A
• gnomAD v3: 6-98875062-AC-A
• gnomAD v4: 6-98875062-AC-A
• MyVariant Identifiers: chr6:g.99322939del (hg19) ; chr6:g.98875063del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875063del , CM000668.2:g.98875063del	GRCh38
NC_000006.11:g.99322939del , CM000668.1:g.99322939del	GRCh37
NC_000006.10:g.99429660del	NCBI36
NG_033903.1:g.77944del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1702+352del MANE Select	ENSP00000358247.1:n.1702+352del
ENST00000229971.2:c.1702+352del	ENSP00000229971.1:n.1702+352del
ENST00000369244.6:c.1702+352del	ENSP00000358247.1:n.1702+352del
NM_001278716.1:c.1702+352del	NP_001265645.1:n.1702+352del
NM_012160.4:c.1702+352del	NP_036292.2:n.1702+352del
NR_103836.1:n.1747+352del
XM_005266930.1:c.1630+352del	XP_005266987.1:n.1630+352del
XM_005266930.3:c.1630+352del	XP_005266987.1:n.1630+352del
XM_017010726.1:c.1702+352del	XP_016866215.1:n.1702+352del
XM_017010727.2:c.1630+352del	XP_016866216.1:n.1630+352del
XM_017010728.1:c.976+352del	XP_016866217.1:n.976+352del
NM_001278716.2:c.1702+352del MANE Select	NP_001265645.1:n.1702+352del
NR_103836.2:n.1687+352del
NM_012160.5:c.1702+352del	NP_036292.2:n.1702+352del