Canonical Allele Identifier: CA2679757733

Gene: FBXL4

Linked Data

• gnomAD v4: 6-98875316-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875317del , CM000668.2:g.98875317del	GRCh38
NC_000006.11:g.99323193del , CM000668.1:g.99323193del	GRCh37
NC_000006.10:g.99429914del	NCBI36
NG_033903.1:g.77690del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1702+98del MANE Select	ENSP00000358247.1:n.1702+98del
ENST00000229971.2:c.1702+98del	ENSP00000229971.1:n.1702+98del
ENST00000369244.6:c.1702+98del	ENSP00000358247.1:n.1702+98del
NM_001278716.1:c.1702+98del	NP_001265645.1:n.1702+98del
NM_012160.4:c.1702+98del	NP_036292.2:n.1702+98del
NR_103836.1:n.1747+98del
XM_005266930.1:c.1630+98del	XP_005266987.1:n.1630+98del
XM_005266930.3:c.1630+98del	XP_005266987.1:n.1630+98del
XM_017010726.1:c.1702+98del	XP_016866215.1:n.1702+98del
XM_017010727.2:c.1630+98del	XP_016866216.1:n.1630+98del
XM_017010728.1:c.976+98del	XP_016866217.1:n.976+98del
NM_001278716.2:c.1702+98del MANE Select	NP_001265645.1:n.1702+98del
NR_103836.2:n.1687+98del
NM_012160.5:c.1702+98del	NP_036292.2:n.1702+98del