Canonical Allele Identifier: CA347974355

Gene: RFX8

Linked Data

• MyVariant Identifiers: chr2:g.102029422C>G (hg19) ; chr2:g.101412960C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.101412960C>G , CM000664.2:g.101412960C>G	GRCh38
NC_000002.11:g.102029422C>G , CM000664.1:g.102029422C>G	GRCh37
NC_000002.10:g.101395854C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646893.2:c.1012G>C	ENSP00000494249.2:p.Asp338His
ENST00000428343.6:c.673G>C MANE Select	ENSP00000401536.1:p.Asp225His
ENST00000646446.1:c.886G>C	ENSP00000494216.1:p.Asp296His
ENST00000646893.1:c.799G>C	ENSP00000494249.1:p.Asp267His
ENST00000428343.5:c.673G>C	ENSP00000401536.1:p.Asp225His
ENST00000481179.5:c.*389G>C	ENSP00000422968.1:n.*389G>C
NM_001145664.1:c.673G>C	NP_001139136.1:p.Asp225His
XM_011511771.1:c.901G>C	XP_011510073.1:p.Asp301His
XM_011511772.1:c.886G>C	XP_011510074.1:p.Asp296His
XM_011511773.1:c.583G>C	XP_011510075.1:p.Asp195His
XM_011511774.1:c.901G>C	XP_011510076.1:p.Asp301His
XM_011511775.1:c.901G>C	XP_011510077.1:p.Asp301His
XM_011511776.1:c.385G>C	XP_011510078.1:p.Asp129His
XM_011511777.1:c.385G>C	XP_011510079.1:p.Asp129His
XM_011511778.1:c.385G>C	XP_011510080.1:p.Asp129His
XM_011511779.1:c.*86G>C	XP_011510081.1:n.*86G>C
XM_011511771.2:c.901G>C	XP_011510073.1:p.Asp301His
XM_011511777.2:c.385G>C	XP_011510079.1:p.Asp129His
XM_017004851.1:c.1012G>C	XP_016860340.1:p.Asp338His
XM_017004852.1:c.799G>C	XP_016860341.1:p.Asp267His
XM_017004853.1:c.1012G>C	XP_016860342.1:p.Asp338His
XM_017004854.1:c.1012G>C	XP_016860343.1:p.Asp338His
XR_001738924.1:n.956G>C
NM_001145664.2:c.673G>C MANE Select	NP_001139136.2:p.Asp225His
NM_001367508.1:c.160G>C	NP_001354437.1:p.Asp54His
NM_001367509.1:c.160G>C	NP_001354438.1:p.Asp54His
NM_001367510.1:c.160G>C	NP_001354439.1:p.Asp54His