Canonical Allele Identifier: CA451573807

Gene: FBXL4

Linked Data

• MyVariant Identifiers: chr6:g.99374834G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98926958G>A , CM000668.2:g.98926958G>A	GRCh38
NC_000006.11:g.99374834G>A , CM000668.1:g.99374834G>A	GRCh37
NC_000006.10:g.99481555G>A	NCBI36
NG_033903.1:g.26049C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.31C>T MANE Select	ENSP00000358247.1:p.Leu11=
ENST00000229971.2:c.31C>T	ENSP00000229971.1:p.Leu11=
ENST00000369244.6:c.31C>T	ENSP00000358247.1:p.Leu11=
NM_001278716.1:c.31C>T	NP_001265645.1:p.Leu11=
NM_012160.4:c.31C>T	NP_036292.2:p.Leu11=
NR_103836.1:n.422C>T
NR_103837.1:n.422C>T
XM_005266930.1:c.31C>T	XP_005266987.1:p.Leu11=
XM_011535748.1:c.31C>T	XP_011534050.1:p.Leu11=
XM_005266930.3:c.31C>T	XP_005266987.1:p.Leu11=
XM_011535748.3:c.31C>T	XP_011534050.1:p.Leu11=
XM_017010726.1:c.31C>T	XP_016866215.1:p.Leu11=
XM_017010727.2:c.31C>T	XP_016866216.1:p.Leu11=
XM_017010728.1:c.-772C>T	XP_016866217.1:n.-772C>T
NM_001278716.2:c.31C>T MANE Select	NP_001265645.1:p.Leu11=
NR_103836.2:n.362C>T
NR_103837.2:n.362C>T
NM_012160.5:c.31C>T	NP_036292.2:p.Leu11=