Canonical Allele Identifier: CA365091219

Gene: FBXL4

Linked Data

• gnomAD v4: 6-98926826-C-A
• MyVariant Identifiers: chr6:g.99374702C>A (hg19) ; chr6:g.98926826C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98926826C>A , CM000668.2:g.98926826C>A	GRCh38
NC_000006.11:g.99374702C>A , CM000668.1:g.99374702C>A	GRCh37
NC_000006.10:g.99481423C>A	NCBI36
NG_033903.1:g.26181G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000369244.7:c.163G>T MANE Select	ENSP00000358247.1:p.Ala55Ser
ENST00000229971.2:c.163G>T	ENSP00000229971.1:p.Ala55Ser
ENST00000369244.6:c.163G>T	ENSP00000358247.1:p.Ala55Ser
NM_001278716.1:c.163G>T	NP_001265645.1:p.Ala55Ser
NM_012160.4:c.163G>T	NP_036292.2:p.Ala55Ser
NR_103836.1:n.554G>T
NR_103837.1:n.554G>T
XM_005266930.1:c.163G>T	XP_005266987.1:p.Ala55Ser
XM_011535748.1:c.163G>T	XP_011534050.1:p.Ala55Ser
XM_005266930.3:c.163G>T	XP_005266987.1:p.Ala55Ser
XM_011535748.3:c.163G>T	XP_011534050.1:p.Ala55Ser
XM_017010726.1:c.163G>T	XP_016866215.1:p.Ala55Ser
XM_017010727.2:c.163G>T	XP_016866216.1:p.Ala55Ser
XM_017010728.1:c.-640G>T	XP_016866217.1:n.-640G>T
NM_001278716.2:c.163G>T MANE Select	NP_001265645.1:p.Ala55Ser
NR_103836.2:n.494G>T
NR_103837.2:n.494G>T
NM_012160.5:c.163G>T	NP_036292.2:p.Ala55Ser