Canonical Allele Identifier: CA830348828

Gene: FBXL4

Linked Data

• dbSNP Id: rs1352943395
• gnomAD v3: 6-98875116-TAGAG-T
• gnomAD v4: 6-98875116-TAGAG-T
• MyVariant Identifiers: chr6:g.99322993_99322996del (hg19) ; chr6:g.98875117_98875120del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875119_98875122del , CM000668.2:g.98875119_98875122del	GRCh38
NC_000006.11:g.99322995_99322998del , CM000668.1:g.99322995_99322998del	GRCh37
NC_000006.10:g.99429716_99429719del	NCBI36
NG_033903.1:g.77887_77890del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1702+295_1702+298del MANE Select	ENSP00000358247.1:n.1702+295_1702+298del
ENST00000229971.2:c.1702+295_1702+298del	ENSP00000229971.1:n.1702+295_1702+298del
ENST00000369244.6:c.1702+295_1702+298del	ENSP00000358247.1:n.1702+295_1702+298del
NM_001278716.1:c.1702+295_1702+298del	NP_001265645.1:n.1702+295_1702+298del
NM_012160.4:c.1702+295_1702+298del	NP_036292.2:n.1702+295_1702+298del
NR_103836.1:n.1747+295_1747+298del
XM_005266930.1:c.1630+295_1630+298del	XP_005266987.1:n.1630+295_1630+298del
XM_005266930.3:c.1630+295_1630+298del	XP_005266987.1:n.1630+295_1630+298del
XM_017010726.1:c.1702+295_1702+298del	XP_016866215.1:n.1702+295_1702+298del
XM_017010727.2:c.1630+295_1630+298del	XP_016866216.1:n.1630+295_1630+298del
XM_017010728.1:c.976+295_976+298del	XP_016866217.1:n.976+295_976+298del
NM_001278716.2:c.1702+295_1702+298del MANE Select	NP_001265645.1:n.1702+295_1702+298del
NR_103836.2:n.1687+295_1687+298del
NM_012160.5:c.1702+295_1702+298del	NP_036292.2:n.1702+295_1702+298del