Canonical Allele Identifier: CA2679757688

Gene: FBXL4

Linked Data

• gnomAD v4: 6-98875201-ATTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875204_98875206del , CM000668.2:g.98875204_98875206del	GRCh38
NC_000006.11:g.99323080_99323082del , CM000668.1:g.99323080_99323082del	GRCh37
NC_000006.10:g.99429801_99429803del	NCBI36
NG_033903.1:g.77803_77805del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1702+211_1702+213del MANE Select	ENSP00000358247.1:n.1702+211_1702+213del
ENST00000229971.2:c.1702+211_1702+213del	ENSP00000229971.1:n.1702+211_1702+213del
ENST00000369244.6:c.1702+211_1702+213del	ENSP00000358247.1:n.1702+211_1702+213del
NM_001278716.1:c.1702+211_1702+213del	NP_001265645.1:n.1702+211_1702+213del
NM_012160.4:c.1702+211_1702+213del	NP_036292.2:n.1702+211_1702+213del
NR_103836.1:n.1747+211_1747+213del
XM_005266930.1:c.1630+211_1630+213del	XP_005266987.1:n.1630+211_1630+213del
XM_005266930.3:c.1630+211_1630+213del	XP_005266987.1:n.1630+211_1630+213del
XM_017010726.1:c.1702+211_1702+213del	XP_016866215.1:n.1702+211_1702+213del
XM_017010727.2:c.1630+211_1630+213del	XP_016866216.1:n.1630+211_1630+213del
XM_017010728.1:c.976+211_976+213del	XP_016866217.1:n.976+211_976+213del
NM_001278716.2:c.1702+211_1702+213del MANE Select	NP_001265645.1:n.1702+211_1702+213del
NR_103836.2:n.1687+211_1687+213del
NM_012160.5:c.1702+211_1702+213del	NP_036292.2:n.1702+211_1702+213del