Canonical Allele Identifier: CA830348809

Gene: FBXL4

Linked Data

• dbSNP Id: rs1178759947
• gnomAD v3: 6-98875071-AATTC-A
• gnomAD v4: 6-98875071-AATTC-A
• MyVariant Identifiers: chr6:g.99322948_99322951del (hg19) ; chr6:g.98875072_98875075del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875075_98875078del , CM000668.2:g.98875075_98875078del	GRCh38
NC_000006.11:g.99322951_99322954del , CM000668.1:g.99322951_99322954del	GRCh37
NC_000006.10:g.99429672_99429675del	NCBI36
NG_033903.1:g.77932_77935del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1702+340_1702+343del MANE Select	ENSP00000358247.1:n.1702+340_1702+343del
ENST00000229971.2:c.1702+340_1702+343del	ENSP00000229971.1:n.1702+340_1702+343del
ENST00000369244.6:c.1702+340_1702+343del	ENSP00000358247.1:n.1702+340_1702+343del
NM_001278716.1:c.1702+340_1702+343del	NP_001265645.1:n.1702+340_1702+343del
NM_012160.4:c.1702+340_1702+343del	NP_036292.2:n.1702+340_1702+343del
NR_103836.1:n.1747+340_1747+343del
XM_005266930.1:c.1630+340_1630+343del	XP_005266987.1:n.1630+340_1630+343del
XM_005266930.3:c.1630+340_1630+343del	XP_005266987.1:n.1630+340_1630+343del
XM_017010726.1:c.1702+340_1702+343del	XP_016866215.1:n.1702+340_1702+343del
XM_017010727.2:c.1630+340_1630+343del	XP_016866216.1:n.1630+340_1630+343del
XM_017010728.1:c.976+340_976+343del	XP_016866217.1:n.976+340_976+343del
NM_001278716.2:c.1702+340_1702+343del MANE Select	NP_001265645.1:n.1702+340_1702+343del
NR_103836.2:n.1687+340_1687+343del
NM_012160.5:c.1702+340_1702+343del	NP_036292.2:n.1702+340_1702+343del