Canonical Allele Identifier: CA451363941

Gene: FBXL4

Linked Data

• gnomAD v4: 6-98926500-G-T
• MyVariant Identifiers: chr6:g.99374376G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98926500G>T , CM000668.2:g.98926500G>T	GRCh38
NC_000006.11:g.99374376G>T , CM000668.1:g.99374376G>T	GRCh37
NC_000006.10:g.99481097G>T	NCBI36
NG_033903.1:g.26507C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.489C>A MANE Select	ENSP00000358247.1:p.Ser163=
ENST00000229971.2:c.489C>A	ENSP00000229971.1:p.Ser163=
ENST00000369244.6:c.489C>A	ENSP00000358247.1:p.Ser163=
NM_001278716.1:c.489C>A	NP_001265645.1:p.Ser163=
NM_012160.4:c.489C>A	NP_036292.2:p.Ser163=
NR_103836.1:n.880C>A
NR_103837.1:n.880C>A
XM_005266930.1:c.489C>A	XP_005266987.1:p.Ser163=
XM_011535748.1:c.489C>A	XP_011534050.1:p.Ser163=
XM_005266930.3:c.489C>A	XP_005266987.1:p.Ser163=
XM_011535748.3:c.489C>A	XP_011534050.1:p.Ser163=
XM_017010726.1:c.489C>A	XP_016866215.1:p.Ser163=
XM_017010727.2:c.489C>A	XP_016866216.1:p.Ser163=
XM_017010728.1:c.-314C>A	XP_016866217.1:n.-314C>A
NM_001278716.2:c.489C>A MANE Select	NP_001265645.1:p.Ser163=
NR_103836.2:n.820C>A
NR_103837.2:n.820C>A
NM_012160.5:c.489C>A	NP_036292.2:p.Ser163=