Canonical Allele Identifier: CA426008149

Gene: FBXO11

Linked Data

• gnomAD v4: 2-47823154-G-A
• MyVariant Identifiers: chr2:g.48050293G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47823154G>A , CM000664.2:g.47823154G>A	GRCh38
NC_000002.11:g.48050293G>A , CM000664.1:g.48050293G>A	GRCh37
NC_000002.10:g.47903797G>A	NCBI36
NG_008397.1:g.87522C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000681999.1:n.1482C>T
ENST00000682451.1:n.1451C>T
ENST00000682975.1:n.1500C>T
ENST00000683894.1:c.1353C>T	ENSP00000507789.1:p.Asp451=
ENST00000684085.1:n.1482C>T
ENST00000684712.1:n.1713C>T
ENST00000403359.8:c.1605C>T MANE Select	ENSP00000384823.4:p.Asp535=
ENST00000316377.8:c.1371C>T	ENSP00000323822.5:p.Asp457=
ENST00000402508.5:c.1353C>T	ENSP00000385398.1:p.Asp451=
ENST00000403359.7:c.1605C>T	ENSP00000384823.3:p.Asp535=
ENST00000492225.5:n.1453C>T
ENST00000493962.6:c.979C>T
NM_001190274.1:c.1605C>T	NP_001177203.1:p.Asp535=
NM_025133.4:c.1353C>T	NP_079409.3:p.Asp451=
XM_005264572.3:c.1605C>T	XP_005264629.1:p.Asp535=
XM_005264573.3:c.1602C>T	XP_005264630.1:p.Asp534=
XM_005264572.5:c.1605C>T	XP_005264629.1:p.Asp535=
XM_005264573.5:c.1602C>T	XP_005264630.1:p.Asp534=
XM_017005015.1:c.1602C>T	XP_016860504.1:p.Asp534=
XM_017005016.2:c.1353C>T	XP_016860505.1:p.Asp451=
XM_017005017.1:c.1353C>T	XP_016860506.1:p.Asp451=
NM_001190274.2:c.1605C>T MANE Select	NP_001177203.1:p.Asp535=
NM_001374325.1:c.1353C>T	NP_001361254.1:p.Asp451=