Canonical Allele Identifier: CA365090113

Gene: FBXL4

Linked Data

• ClinVar Variation Id: 3093541
• ClinVar RCV Id: RCV004378914
• gnomAD v4: 6-98926720-T-C
• MyVariant Identifiers: chr6:g.99374596T>C (hg19) ; chr6:g.98926720T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98926720T>C , CM000668.2:g.98926720T>C	GRCh38
NC_000006.11:g.99374596T>C , CM000668.1:g.99374596T>C	GRCh37
NC_000006.10:g.99481317T>C	NCBI36
NG_033903.1:g.26287A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.269A>G MANE Select	ENSP00000358247.1:p.Asp90Gly
ENST00000229971.2:c.269A>G	ENSP00000229971.1:p.Asp90Gly
ENST00000369244.6:c.269A>G	ENSP00000358247.1:p.Asp90Gly
NM_001278716.1:c.269A>G	NP_001265645.1:p.Asp90Gly
NM_012160.4:c.269A>G	NP_036292.2:p.Asp90Gly
NR_103836.1:n.660A>G
NR_103837.1:n.660A>G
XM_005266930.1:c.269A>G	XP_005266987.1:p.Asp90Gly
XM_011535748.1:c.269A>G	XP_011534050.1:p.Asp90Gly
XM_005266930.3:c.269A>G	XP_005266987.1:p.Asp90Gly
XM_011535748.3:c.269A>G	XP_011534050.1:p.Asp90Gly
XM_017010726.1:c.269A>G	XP_016866215.1:p.Asp90Gly
XM_017010727.2:c.269A>G	XP_016866216.1:p.Asp90Gly
XM_017010728.1:c.-534A>G	XP_016866217.1:n.-534A>G
NM_001278716.2:c.269A>G MANE Select	NP_001265645.1:p.Asp90Gly
NR_103836.2:n.600A>G
NR_103837.2:n.600A>G
NM_012160.5:c.269A>G	NP_036292.2:p.Asp90Gly