Canonical Allele Identifier: CA1274778578

Gene: RFX8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.101412949G= , CM000664.2:g.101412949G=	GRCh38
NC_000002.11:g.102029411G= , CM000664.1:g.102029411G=	GRCh37
NC_000002.10:g.101395843G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646893.2:c.1023C=	ENSP00000494249.2:p.Gly341=
ENST00000428343.6:c.684C= MANE Select	ENSP00000401536.1:p.Gly228=
ENST00000646446.1:c.897C=	ENSP00000494216.1:p.Gly299=
ENST00000646893.1:c.810C=	ENSP00000494249.1:p.Gly270=
ENST00000428343.5:c.684C=	ENSP00000401536.1:p.Gly228=
ENST00000481179.5:c.*400C=	ENSP00000422968.1:n.*400C=
NM_001145664.1:c.684C=	NP_001139136.1:p.Gly228=
XM_011511771.1:c.912C=	XP_011510073.1:p.Gly304=
XM_011511772.1:c.897C=	XP_011510074.1:p.Gly299=
XM_011511773.1:c.594C=	XP_011510075.1:p.Gly198=
XM_011511774.1:c.912C=	XP_011510076.1:p.Gly304=
XM_011511775.1:c.912C=	XP_011510077.1:p.Gly304=
XM_011511776.1:c.396C=	XP_011510078.1:p.Gly132=
XM_011511777.1:c.396C=	XP_011510079.1:p.Gly132=
XM_011511778.1:c.396C=	XP_011510080.1:p.Gly132=
XM_011511779.1:c.*97C=	XP_011510081.1:n.*97C=
XM_011511771.2:c.912C=	XP_011510073.1:p.Gly304=
XM_011511777.2:c.396C=	XP_011510079.1:p.Gly132=
XM_017004851.1:c.1023C=	XP_016860340.1:p.Gly341=
XM_017004852.1:c.810C=	XP_016860341.1:p.Gly270=
XM_017004853.1:c.1023C=	XP_016860342.1:p.Gly341=
XM_017004854.1:c.1023C=	XP_016860343.1:p.Gly341=
XR_001738924.1:n.967C=
NM_001145664.2:c.684C= MANE Select	NP_001139136.2:p.Gly228=
NM_001367508.1:c.171C=	NP_001354437.1:p.Gly57=
NM_001367509.1:c.171C=	NP_001354438.1:p.Gly57=
NM_001367510.1:c.171C=	NP_001354439.1:p.Gly57=