Canonical Allele Identifier: CA2679757680

Gene: FBXL4

Linked Data

• gnomAD v4: 6-98875183-TAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875185_98875186del , CM000668.2:g.98875185_98875186del	GRCh38
NC_000006.11:g.99323061_99323062del , CM000668.1:g.99323061_99323062del	GRCh37
NC_000006.10:g.99429782_99429783del	NCBI36
NG_033903.1:g.77822_77823del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1702+230_1702+231del MANE Select	ENSP00000358247.1:n.1702+230_1702+231del
ENST00000229971.2:c.1702+230_1702+231del	ENSP00000229971.1:n.1702+230_1702+231del
ENST00000369244.6:c.1702+230_1702+231del	ENSP00000358247.1:n.1702+230_1702+231del
NM_001278716.1:c.1702+230_1702+231del	NP_001265645.1:n.1702+230_1702+231del
NM_012160.4:c.1702+230_1702+231del	NP_036292.2:n.1702+230_1702+231del
NR_103836.1:n.1747+230_1747+231del
XM_005266930.1:c.1630+230_1630+231del	XP_005266987.1:n.1630+230_1630+231del
XM_005266930.3:c.1630+230_1630+231del	XP_005266987.1:n.1630+230_1630+231del
XM_017010726.1:c.1702+230_1702+231del	XP_016866215.1:n.1702+230_1702+231del
XM_017010727.2:c.1630+230_1630+231del	XP_016866216.1:n.1630+230_1630+231del
XM_017010728.1:c.976+230_976+231del	XP_016866217.1:n.976+230_976+231del
NM_001278716.2:c.1702+230_1702+231del MANE Select	NP_001265645.1:n.1702+230_1702+231del
NR_103836.2:n.1687+230_1687+231del
NM_012160.5:c.1702+230_1702+231del	NP_036292.2:n.1702+230_1702+231del