Canonical Allele Identifier: CA2699721640
Gene: RFX8 HGNC NCBI

Linked Data

dbSNP Id: rs1408859823

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.101413226dup , CM000664.2:g.101413226dup GRCh38
NC_000002.11:g.102029688dup , CM000664.1:g.102029688dup GRCh37
NC_000002.10:g.101396120dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000646893.2:c.901-152dup ENSP00000494249.2:n.901-152dup
ENST00000428343.6:c.562-152dup MANE Select ENSP00000401536.1:n.562-152dup
ENST00000646446.1:c.775-152dup ENSP00000494216.1:n.775-152dup
ENST00000646893.1:c.688-152dup ENSP00000494249.1:n.688-152dup
ENST00000428343.5:c.562-152dup ENSP00000401536.1:n.562-152dup
ENST00000481179.5:c.*278-152dup ENSP00000422968.1:n.*278-152dup
NM_001145664.1:c.562-152dup NP_001139136.1:n.562-152dup
XM_011511771.1:c.790-152dup XP_011510073.1:n.790-152dup
XM_011511772.1:c.775-152dup XP_011510074.1:n.775-152dup
XM_011511773.1:c.472-152dup XP_011510075.1:n.472-152dup
XM_011511774.1:c.790-152dup XP_011510076.1:n.790-152dup
XM_011511775.1:c.790-152dup XP_011510077.1:n.790-152dup
XM_011511776.1:c.274-152dup XP_011510078.1:n.274-152dup
XM_011511777.1:c.274-152dup XP_011510079.1:n.274-152dup
XM_011511778.1:c.274-152dup XP_011510080.1:n.274-152dup
XM_011511779.1:c.731-152dup XP_011510081.1:n.731-152dup
XM_011511771.2:c.790-152dup XP_011510073.1:n.790-152dup
XM_011511777.2:c.274-152dup XP_011510079.1:n.274-152dup
XM_017004851.1:c.901-152dup XP_016860340.1:n.901-152dup
XM_017004852.1:c.688-152dup XP_016860341.1:n.688-152dup
XM_017004853.1:c.901-152dup XP_016860342.1:n.901-152dup
XM_017004854.1:c.901-152dup XP_016860343.1:n.901-152dup
XR_001738924.1:n.845-152dup
NM_001145664.2:c.562-152dup MANE Select NP_001139136.2:n.562-152dup
NM_001367508.1:c.49-152dup NP_001354437.1:n.49-152dup
NM_001367509.1:c.49-152dup NP_001354438.1:n.49-152dup
NM_001367510.1:c.49-152dup NP_001354439.1:n.49-152dup