Canonical Allele Identifier: CA16021062

Gene: FBXL4

Linked Data

• dbSNP Id: rs1312430975
• gnomAD v2: 6-99323371-G-GT
• gnomAD v4: 6-98875495-G-GT
• MyVariant Identifiers: chr6:g.99323371_99323372insT (hg19) ; chr6:g.98875495_98875496insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875496dup , CM000668.2:g.98875496dup	GRCh38
NC_000006.11:g.99323372dup , CM000668.1:g.99323372dup	GRCh37
NC_000006.10:g.99430093dup	NCBI36
NG_033903.1:g.77511dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1621dup MANE Select	ENSP00000358247.1:p.Thr541AsnfsTer3
ENST00000229971.2:c.1621dup	ENSP00000229971.1:p.Thr541AsnfsTer3
ENST00000369244.6:c.1621dup	ENSP00000358247.1:p.Thr541AsnfsTer3
NM_001278716.1:c.1621dup	NP_001265645.1:p.Thr541AsnfsTer3
NM_012160.4:c.1621dup	NP_036292.2:p.Thr541AsnfsTer3
NR_103836.1:n.1666dup
XM_005266930.1:c.1549dup	XP_005266987.1:p.Thr517AsnfsTer3
XM_005266930.3:c.1549dup	XP_005266987.1:p.Thr517AsnfsTer3
XM_017010726.1:c.1621dup	XP_016866215.1:p.Thr541AsnfsTer3
XM_017010727.2:c.1549dup	XP_016866216.1:p.Thr517AsnfsTer3
XM_017010728.1:c.895dup	XP_016866217.1:p.Thr299AsnfsTer3
NM_001278716.2:c.1621dup MANE Select	NP_001265645.1:p.Thr541AsnfsTer3
NR_103836.2:n.1606dup
NM_012160.5:c.1621dup	NP_036292.2:p.Thr541AsnfsTer3