Canonical Allele Identifier: CA347974396

Gene: RFX8

Linked Data

• MyVariant Identifiers: chr2:g.102029440T>G (hg19) ; chr2:g.101412978T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.101412978T>G , CM000664.2:g.101412978T>G	GRCh38
NC_000002.11:g.102029440T>G , CM000664.1:g.102029440T>G	GRCh37
NC_000002.10:g.101395872T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646893.2:c.994A>C	ENSP00000494249.2:p.Lys332Gln
ENST00000428343.6:c.655A>C MANE Select	ENSP00000401536.1:p.Lys219Gln
ENST00000646446.1:c.868A>C	ENSP00000494216.1:p.Lys290Gln
ENST00000646893.1:c.781A>C	ENSP00000494249.1:p.Lys261Gln
ENST00000428343.5:c.655A>C	ENSP00000401536.1:p.Lys219Gln
ENST00000481179.5:c.*371A>C	ENSP00000422968.1:n.*371A>C
NM_001145664.1:c.655A>C	NP_001139136.1:p.Lys219Gln
XM_011511771.1:c.883A>C	XP_011510073.1:p.Lys295Gln
XM_011511772.1:c.868A>C	XP_011510074.1:p.Lys290Gln
XM_011511773.1:c.565A>C	XP_011510075.1:p.Lys189Gln
XM_011511774.1:c.883A>C	XP_011510076.1:p.Lys295Gln
XM_011511775.1:c.883A>C	XP_011510077.1:p.Lys295Gln
XM_011511776.1:c.367A>C	XP_011510078.1:p.Lys123Gln
XM_011511777.1:c.367A>C	XP_011510079.1:p.Lys123Gln
XM_011511778.1:c.367A>C	XP_011510080.1:p.Lys123Gln
XM_011511779.1:c.*68A>C	XP_011510081.1:n.*68A>C
XM_011511771.2:c.883A>C	XP_011510073.1:p.Lys295Gln
XM_011511777.2:c.367A>C	XP_011510079.1:p.Lys123Gln
XM_017004851.1:c.994A>C	XP_016860340.1:p.Lys332Gln
XM_017004852.1:c.781A>C	XP_016860341.1:p.Lys261Gln
XM_017004853.1:c.994A>C	XP_016860342.1:p.Lys332Gln
XM_017004854.1:c.994A>C	XP_016860343.1:p.Lys332Gln
XR_001738924.1:n.938A>C
NM_001145664.2:c.655A>C MANE Select	NP_001139136.2:p.Lys219Gln
NM_001367508.1:c.142A>C	NP_001354437.1:p.Lys48Gln
NM_001367509.1:c.142A>C	NP_001354438.1:p.Lys48Gln
NM_001367510.1:c.142A>C	NP_001354439.1:p.Lys48Gln