Canonical Allele Identifier: CA347974289

Gene: RFX8

Linked Data

• MyVariant Identifiers: chr2:g.102029392T>C (hg19) ; chr2:g.101412930T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.101412930T>C , CM000664.2:g.101412930T>C	GRCh38
NC_000002.11:g.102029392T>C , CM000664.1:g.102029392T>C	GRCh37
NC_000002.10:g.101395824T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646893.2:c.1042A>G	ENSP00000494249.2:p.Asn348Asp
ENST00000428343.6:c.703A>G MANE Select	ENSP00000401536.1:p.Asn235Asp
ENST00000646446.1:c.916A>G	ENSP00000494216.1:p.Asn306Asp
ENST00000646893.1:c.829A>G	ENSP00000494249.1:p.Asn277Asp
ENST00000428343.5:c.703A>G	ENSP00000401536.1:p.Asn235Asp
ENST00000481179.5:c.*419A>G	ENSP00000422968.1:n.*419A>G
NM_001145664.1:c.703A>G	NP_001139136.1:p.Asn235Asp
XM_011511771.1:c.931A>G	XP_011510073.1:p.Asn311Asp
XM_011511772.1:c.916A>G	XP_011510074.1:p.Asn306Asp
XM_011511773.1:c.613A>G	XP_011510075.1:p.Asn205Asp
XM_011511774.1:c.931A>G	XP_011510076.1:p.Asn311Asp
XM_011511775.1:c.931A>G	XP_011510077.1:p.Asn311Asp
XM_011511776.1:c.415A>G	XP_011510078.1:p.Asn139Asp
XM_011511777.1:c.415A>G	XP_011510079.1:p.Asn139Asp
XM_011511778.1:c.415A>G	XP_011510080.1:p.Asn139Asp
XM_011511771.2:c.931A>G	XP_011510073.1:p.Asn311Asp
XM_011511777.2:c.415A>G	XP_011510079.1:p.Asn139Asp
XM_017004851.1:c.1042A>G	XP_016860340.1:p.Asn348Asp
XM_017004852.1:c.829A>G	XP_016860341.1:p.Asn277Asp
XM_017004853.1:c.1042A>G	XP_016860342.1:p.Asn348Asp
XM_017004854.1:c.1042A>G	XP_016860343.1:p.Asn348Asp
XR_001738924.1:n.986A>G
NM_001145664.2:c.703A>G MANE Select	NP_001139136.2:p.Asn235Asp
NM_001367508.1:c.190A>G	NP_001354437.1:p.Asn64Asp
NM_001367509.1:c.190A>G	NP_001354438.1:p.Asn64Asp
NM_001367510.1:c.190A>G	NP_001354439.1:p.Asn64Asp