Canonical Allele Identifier: CA347974553
Gene: RFX8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.101413051T>G , CM000664.2:g.101413051T>G GRCh38
NC_000002.11:g.102029513T>G , CM000664.1:g.102029513T>G GRCh37
NC_000002.10:g.101395945T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000646893.2:c.921A>C ENSP00000494249.2:p.Lys307Asn
ENST00000428343.6:c.582A>C MANE Select ENSP00000401536.1:p.Lys194Asn
ENST00000646446.1:c.795A>C ENSP00000494216.1:p.Lys265Asn
ENST00000646893.1:c.708A>C ENSP00000494249.1:p.Lys236Asn
ENST00000428343.5:c.582A>C ENSP00000401536.1:p.Lys194Asn
ENST00000481179.5:c.*298A>C ENSP00000422968.1:n.*298A>C
NM_001145664.1:c.582A>C NP_001139136.1:p.Lys194Asn
XM_011511771.1:c.810A>C XP_011510073.1:p.Lys270Asn
XM_011511772.1:c.795A>C XP_011510074.1:p.Lys265Asn
XM_011511773.1:c.492A>C XP_011510075.1:p.Lys164Asn
XM_011511774.1:c.810A>C XP_011510076.1:p.Lys270Asn
XM_011511775.1:c.810A>C XP_011510077.1:p.Lys270Asn
XM_011511776.1:c.294A>C XP_011510078.1:p.Lys98Asn
XM_011511777.1:c.294A>C XP_011510079.1:p.Lys98Asn
XM_011511778.1:c.294A>C XP_011510080.1:p.Lys98Asn
XM_011511779.1:c.751A>C XP_011510081.1:p.Lys251Gln
XM_011511771.2:c.810A>C XP_011510073.1:p.Lys270Asn
XM_011511777.2:c.294A>C XP_011510079.1:p.Lys98Asn
XM_017004851.1:c.921A>C XP_016860340.1:p.Lys307Asn
XM_017004852.1:c.708A>C XP_016860341.1:p.Lys236Asn
XM_017004853.1:c.921A>C XP_016860342.1:p.Lys307Asn
XM_017004854.1:c.921A>C XP_016860343.1:p.Lys307Asn
XR_001738924.1:n.865A>C
NM_001145664.2:c.582A>C MANE Select NP_001139136.2:p.Lys194Asn
NM_001367508.1:c.69A>C NP_001354437.1:p.Lys23Asn
NM_001367509.1:c.69A>C NP_001354438.1:p.Lys23Asn
NM_001367510.1:c.69A>C NP_001354439.1:p.Lys23Asn