Canonical Allele Identifier: CA830348794

Gene: FBXL4

Linked Data

• dbSNP Id: rs1055296720
• gnomAD v3: 6-98875054-TA-T
• gnomAD v4: 6-98875054-TA-T
• MyVariant Identifiers: chr6:g.99322931del (hg19) ; chr6:g.98875055del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875062del , CM000668.2:g.98875062del	GRCh38
NC_000006.11:g.99322938del , CM000668.1:g.99322938del	GRCh37
NC_000006.10:g.99429659del	NCBI36
NG_033903.1:g.77952del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1702+360del MANE Select	ENSP00000358247.1:n.1702+360del
ENST00000229971.2:c.1702+360del	ENSP00000229971.1:n.1702+360del
ENST00000369244.6:c.1702+360del	ENSP00000358247.1:n.1702+360del
NM_001278716.1:c.1702+360del	NP_001265645.1:n.1702+360del
NM_012160.4:c.1702+360del	NP_036292.2:n.1702+360del
NR_103836.1:n.1747+360del
XM_005266930.1:c.1630+360del	XP_005266987.1:n.1630+360del
XM_005266930.3:c.1630+360del	XP_005266987.1:n.1630+360del
XM_017010726.1:c.1702+360del	XP_016866215.1:n.1702+360del
XM_017010727.2:c.1630+360del	XP_016866216.1:n.1630+360del
XM_017010728.1:c.976+360del	XP_016866217.1:n.976+360del
NM_001278716.2:c.1702+360del MANE Select	NP_001265645.1:n.1702+360del
NR_103836.2:n.1687+360del
NM_012160.5:c.1702+360del	NP_036292.2:n.1702+360del