Canonical Allele Identifier: CA2679757499

Gene: FBXL4

Linked Data

• gnomAD v4: 6-98874191-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98874195del , CM000668.2:g.98874195del	GRCh38
NC_000006.11:g.99322071del , CM000668.1:g.99322071del	GRCh37
NC_000006.10:g.99428792del	NCBI36
NG_033903.1:g.78815del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.*86del MANE Select	ENSP00000358247.1:n.*86del
ENST00000229971.2:c.*86del	ENSP00000229971.1:n.*86del
ENST00000369244.6:c.*86del	ENSP00000358247.1:n.*86del
NM_001278716.1:c.*86del	NP_001265645.1:n.*86del
NM_012160.4:c.*86del	NP_036292.2:n.*86del
NR_103836.1:n.1997del
XM_005266930.1:c.*86del	XP_005266987.1:n.*86del
XM_005266930.3:c.*86del	XP_005266987.1:n.*86del
XM_017010726.1:c.*86del	XP_016866215.1:n.*86del
XM_017010727.2:c.*86del	XP_016866216.1:n.*86del
XM_017010728.1:c.*86del	XP_016866217.1:n.*86del
NM_001278716.2:c.*86del MANE Select	NP_001265645.1:n.*86del
NR_103836.2:n.1937del
NM_012160.5:c.*86del	NP_036292.2:n.*86del