Canonical Allele Identifier: CA2007079557
Gene: FOXRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126275000G= , CM000673.2:g.126275000G= GRCh38
NC_000011.9:g.126144895G= , CM000673.1:g.126144895G= GRCh37
NC_000011.8:g.125650105G= NCBI36
NG_028029.1:g.10961G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.788G=
ENST00000532101.6:n.734-327G=
ENST00000532125.2:c.607G= ENSP00000434178.2:p.Gly203=
ENST00000533839.6:c.86-794G= ENSP00000509952.1:n.86-794G=
ENST00000534011.6:n.902G=
ENST00000685484.1:c.610G= ENSP00000510622.1:p.Gly204=
ENST00000685601.1:c.610G= ENSP00000510603.1:p.Gly204=
ENST00000685765.1:c.610G= ENSP00000509991.1:p.Gly204=
ENST00000685844.1:c.*169-327G= ENSP00000509820.1:n.*169-327G=
ENST00000685857.1:n.1044G=
ENST00000686242.1:c.409G= ENSP00000508950.1:n.409G=
ENST00000686888.1:c.*177G= ENSP00000509619.1:n.*177G=
ENST00000687699.1:c.734G= ENSP00000508878.1:n.734G=
ENST00000687786.1:n.2068-327G=
ENST00000688100.1:n.1531G=
ENST00000688588.1:c.610G= ENSP00000510802.1:p.Gly204=
ENST00000688927.1:n.2516G=
ENST00000689283.1:c.*273G= ENSP00000509050.1:n.*273G=
ENST00000689477.1:c.*503G= ENSP00000508945.1:n.*503G=
ENST00000689765.1:c.*169-371G= ENSP00000509625.1:n.*169-371G=
ENST00000690512.1:c.*461G= ENSP00000509793.1:n.*461G=
ENST00000692039.1:c.*408G= ENSP00000508821.1:n.*408G=
ENST00000692336.1:c.634G= ENSP00000508540.1:p.Gly212=
ENST00000693133.1:n.785G=
ENST00000263578.10:c.610G= MANE Select ENSP00000263578.5:p.Gly204=
ENST00000263578.9:c.610G= ENSP00000263578.5:p.Gly204=
ENST00000524751.5:n.546G=
ENST00000525083.5:n.352-327G=
ENST00000525770.5:c.*242G= ENSP00000434739.1:n.*242G=
ENST00000526366.5:n.541G=
ENST00000527004.5:c.534-327G= ENSP00000436374.1:n.534-327G=
ENST00000527875.1:n.440G=
ENST00000530642.1:n.1087G=
ENST00000532101.5:n.833G=
ENST00000532125.1:c.568G= ENSP00000434178.1:p.Gly190=
ENST00000533395.5:n.365-327G=
ENST00000533839.5:n.238-794G=
ENST00000534011.5:n.662G=
ENST00000534315.5:n.944-327G=
NM_017547.3:c.610G= NP_060017.1:p.Gly204=
NR_037647.1:n.556G=
NR_037648.1:n.796G=
XM_006718879.2:c.100G= XP_006718942.1:p.Gly34=
XM_006718880.2:c.-2-327G= XP_006718943.1:n.-2-327G=
XM_006718881.2:c.-2-327G= XP_006718944.1:n.-2-327G=
XM_011542895.1:c.100G= XP_011541197.1:p.Gly34=
XM_011542896.1:c.100G= XP_011541198.1:p.Gly34=
XM_006718879.3:c.100G= XP_006718942.1:p.Gly34=
XM_006718881.3:c.-2-327G= XP_006718944.1:n.-2-327G=
XM_011542895.2:c.100G= XP_011541197.1:p.Gly34=
XM_011542896.2:c.100G= XP_011541198.1:p.Gly34=
XM_017018000.2:c.610G= XP_016873489.1:p.Gly204=
XM_017018001.1:c.100G= XP_016873490.1:p.Gly34=
XM_017018002.1:c.100G= XP_016873491.1:p.Gly34=
XM_017018003.2:c.-2-327G= XP_016873492.1:n.-2-327G=
XM_017018004.1:c.-2-327G= XP_016873493.1:n.-2-327G=
XM_017018005.1:c.-2-327G= XP_016873494.1:n.-2-327G=
XM_017018006.2:c.-2-327G= XP_016873495.1:n.-2-327G=
NM_017547.4:c.610G= MANE Select NP_060017.1:p.Gly204=
NR_037647.2:n.442G=
NR_037648.2:n.787G=