Canonical Allele Identifier: CA451573266

Gene: FBXL4

Linked Data

• MyVariant Identifiers: chr6:g.99323442A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875566A>G , CM000668.2:g.98875566A>G	GRCh38
NC_000006.11:g.99323442A>G , CM000668.1:g.99323442A>G	GRCh37
NC_000006.10:g.99430163A>G	NCBI36
NG_033903.1:g.77441T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1551T>C MANE Select	ENSP00000358247.1:p.Thr517=
ENST00000229971.2:c.1551T>C	ENSP00000229971.1:p.Thr517=
ENST00000369244.6:c.1551T>C	ENSP00000358247.1:p.Thr517=
NM_001278716.1:c.1551T>C	NP_001265645.1:p.Thr517=
NM_012160.4:c.1551T>C	NP_036292.2:p.Thr517=
NR_103836.1:n.1596T>C
XM_005266930.1:c.1479T>C	XP_005266987.1:p.Thr493=
XM_005266930.3:c.1479T>C	XP_005266987.1:p.Thr493=
XM_017010726.1:c.1551T>C	XP_016866215.1:p.Thr517=
XM_017010727.2:c.1479T>C	XP_016866216.1:p.Thr493=
XM_017010728.1:c.825T>C	XP_016866217.1:p.Thr275=
NM_001278716.2:c.1551T>C MANE Select	NP_001265645.1:p.Thr517=
NR_103836.2:n.1536T>C
NM_012160.5:c.1551T>C	NP_036292.2:p.Thr517=