Canonical Allele Identifier: CA347974271

Gene: RFX8

Linked Data

• MyVariant Identifiers: chr2:g.102029385T>A (hg19) ; chr2:g.101412923T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.101412923T>A , CM000664.2:g.101412923T>A	GRCh38
NC_000002.11:g.102029385T>A , CM000664.1:g.102029385T>A	GRCh37
NC_000002.10:g.101395817T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646893.2:c.1049A>T	ENSP00000494249.2:p.Glu350Val
ENST00000428343.6:c.710A>T MANE Select	ENSP00000401536.1:p.Glu237Val
ENST00000646446.1:c.923A>T	ENSP00000494216.1:p.Glu308Val
ENST00000646893.1:c.836A>T	ENSP00000494249.1:p.Glu279Val
ENST00000428343.5:c.710A>T	ENSP00000401536.1:p.Glu237Val
ENST00000481179.5:c.*426A>T	ENSP00000422968.1:n.*426A>T
NM_001145664.1:c.710A>T	NP_001139136.1:p.Glu237Val
XM_011511771.1:c.938A>T	XP_011510073.1:p.Glu313Val
XM_011511772.1:c.923A>T	XP_011510074.1:p.Glu308Val
XM_011511773.1:c.620A>T	XP_011510075.1:p.Glu207Val
XM_011511774.1:c.938A>T	XP_011510076.1:p.Glu313Val
XM_011511775.1:c.938A>T	XP_011510077.1:p.Glu313Val
XM_011511776.1:c.422A>T	XP_011510078.1:p.Glu141Val
XM_011511777.1:c.422A>T	XP_011510079.1:p.Glu141Val
XM_011511778.1:c.422A>T	XP_011510080.1:p.Glu141Val
XM_011511771.2:c.938A>T	XP_011510073.1:p.Glu313Val
XM_011511777.2:c.422A>T	XP_011510079.1:p.Glu141Val
XM_017004851.1:c.1049A>T	XP_016860340.1:p.Glu350Val
XM_017004852.1:c.836A>T	XP_016860341.1:p.Glu279Val
XM_017004853.1:c.1049A>T	XP_016860342.1:p.Glu350Val
XM_017004854.1:c.1049A>T	XP_016860343.1:p.Glu350Val
XR_001738924.1:n.993A>T
NM_001145664.2:c.710A>T MANE Select	NP_001139136.2:p.Glu237Val
NM_001367508.1:c.197A>T	NP_001354437.1:p.Glu66Val
NM_001367509.1:c.197A>T	NP_001354438.1:p.Glu66Val
NM_001367510.1:c.197A>T	NP_001354439.1:p.Glu66Val