Canonical Allele Identifier: CA2007079696
Gene: FOXRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126275338G= , CM000673.2:g.126275338G= GRCh38
NC_000011.9:g.126145233G= , CM000673.1:g.126145233G= GRCh37
NC_000011.8:g.125650443G= NCBI36
NG_028029.1:g.11299G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.1126G=
ENST00000532101.6:n.745G=
ENST00000532125.2:c.640G= ENSP00000434178.2:p.Glu214=
ENST00000533839.6:c.86-456G= ENSP00000509952.1:n.86-456G=
ENST00000534011.6:n.935G=
ENST00000685484.1:c.643G= ENSP00000510622.1:p.Glu215=
ENST00000685601.1:c.643G= ENSP00000510603.1:p.Glu215=
ENST00000685765.1:c.643G= ENSP00000509991.1:p.Glu215=
ENST00000685844.1:c.*180G= ENSP00000509820.1:n.*180G=
ENST00000685857.1:n.1382G=
ENST00000686242.1:c.442G= ENSP00000508950.1:n.442G=
ENST00000686888.1:c.*210G= ENSP00000509619.1:n.*210G=
ENST00000687699.1:c.767G= ENSP00000508878.1:n.767G=
ENST00000687786.1:n.2079G=
ENST00000688100.1:n.1564G=
ENST00000688588.1:c.643G= ENSP00000510802.1:p.Glu215=
ENST00000688927.1:n.2854G=
ENST00000689283.1:c.*306G= ENSP00000509050.1:n.*306G=
ENST00000689477.1:c.*536G= ENSP00000508945.1:n.*536G=
ENST00000689765.1:c.*169-33G= ENSP00000509625.1:n.*169-33G=
ENST00000690512.1:c.*494G= ENSP00000509793.1:n.*494G=
ENST00000692039.1:c.*441G= ENSP00000508821.1:n.*441G=
ENST00000692336.1:c.667G= ENSP00000508540.1:p.Glu223=
ENST00000693133.1:n.1123G=
ENST00000263578.10:c.643G= MANE Select ENSP00000263578.5:p.Glu215=
ENST00000263578.9:c.643G= ENSP00000263578.5:p.Glu215=
ENST00000524751.5:n.884G=
ENST00000525083.5:n.363G=
ENST00000525770.5:c.*275G= ENSP00000434739.1:n.*275G=
ENST00000527004.5:c.545G= ENSP00000436374.1:p.Arg182=
ENST00000530642.1:n.1425G=
ENST00000532101.5:n.866G=
ENST00000532125.1:c.601G= ENSP00000434178.1:p.Glu201=
ENST00000533395.5:n.376G=
ENST00000533839.5:n.238-456G=
ENST00000534011.5:n.695G=
ENST00000534315.5:n.955G=
NM_017547.3:c.643G= NP_060017.1:p.Glu215=
NR_037647.1:n.589G=
NR_037648.1:n.829G=
XM_006718879.2:c.133G= XP_006718942.1:p.Glu45=
XM_006718880.2:c.10G= XP_006718943.1:p.Glu4=
XM_006718881.2:c.10G= XP_006718944.1:p.Glu4=
XM_011542895.1:c.133G= XP_011541197.1:p.Glu45=
XM_011542896.1:c.133G= XP_011541198.1:p.Glu45=
XM_006718879.3:c.133G= XP_006718942.1:p.Glu45=
XM_006718881.3:c.10G= XP_006718944.1:p.Glu4=
XM_011542895.2:c.133G= XP_011541197.1:p.Glu45=
XM_011542896.2:c.133G= XP_011541198.1:p.Glu45=
XM_017018000.2:c.643G= XP_016873489.1:p.Glu215=
XM_017018001.1:c.133G= XP_016873490.1:p.Glu45=
XM_017018002.1:c.133G= XP_016873491.1:p.Glu45=
XM_017018003.2:c.10G= XP_016873492.1:p.Glu4=
XM_017018004.1:c.10G= XP_016873493.1:p.Glu4=
XM_017018005.1:c.10G= XP_016873494.1:p.Glu4=
XM_017018006.2:c.10G= XP_016873495.1:p.Glu4=
NM_017547.4:c.643G= MANE Select NP_060017.1:p.Glu215=
NR_037647.2:n.475G=
NR_037648.2:n.820G=