Canonical Allele Identifier: CA427793748

Gene: RFX8

Linked Data

• MyVariant Identifiers: chr2:g.102029501A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.101413039A>C , CM000664.2:g.101413039A>C	GRCh38
NC_000002.11:g.102029501A>C , CM000664.1:g.102029501A>C	GRCh37
NC_000002.10:g.101395933A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646893.2:c.933T>G	ENSP00000494249.2:p.Arg311=
ENST00000428343.6:c.594T>G MANE Select	ENSP00000401536.1:p.Arg198=
ENST00000646446.1:c.807T>G	ENSP00000494216.1:p.Arg269=
ENST00000646893.1:c.720T>G	ENSP00000494249.1:p.Arg240=
ENST00000428343.5:c.594T>G	ENSP00000401536.1:p.Arg198=
ENST00000481179.5:c.*310T>G	ENSP00000422968.1:n.*310T>G
NM_001145664.1:c.594T>G	NP_001139136.1:p.Arg198=
XM_011511771.1:c.822T>G	XP_011510073.1:p.Arg274=
XM_011511772.1:c.807T>G	XP_011510074.1:p.Arg269=
XM_011511773.1:c.504T>G	XP_011510075.1:p.Arg168=
XM_011511774.1:c.822T>G	XP_011510076.1:p.Arg274=
XM_011511775.1:c.822T>G	XP_011510077.1:p.Arg274=
XM_011511776.1:c.306T>G	XP_011510078.1:p.Arg102=
XM_011511777.1:c.306T>G	XP_011510079.1:p.Arg102=
XM_011511778.1:c.306T>G	XP_011510080.1:p.Arg102=
XM_011511779.1:c.*7T>G	XP_011510081.1:n.*7T>G
XM_011511771.2:c.822T>G	XP_011510073.1:p.Arg274=
XM_011511777.2:c.306T>G	XP_011510079.1:p.Arg102=
XM_017004851.1:c.933T>G	XP_016860340.1:p.Arg311=
XM_017004852.1:c.720T>G	XP_016860341.1:p.Arg240=
XM_017004853.1:c.933T>G	XP_016860342.1:p.Arg311=
XM_017004854.1:c.933T>G	XP_016860343.1:p.Arg311=
XR_001738924.1:n.877T>G
NM_001145664.2:c.594T>G MANE Select	NP_001139136.2:p.Arg198=
NM_001367508.1:c.81T>G	NP_001354437.1:p.Arg27=
NM_001367509.1:c.81T>G	NP_001354438.1:p.Arg27=
NM_001367510.1:c.81T>G	NP_001354439.1:p.Arg27=