Canonical Allele Identifier: CA2007079726
Gene: FOXRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126275412C= , CM000673.2:g.126275412C= GRCh38
NC_000011.9:g.126145307C= , CM000673.1:g.126145307C= GRCh37
NC_000011.8:g.125650517C= NCBI36
NG_028029.1:g.11373C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.1200C=
ENST00000532101.6:n.819C=
ENST00000532125.2:c.714C= ENSP00000434178.2:p.Cys238=
ENST00000533839.6:c.86-382C= ENSP00000509952.1:n.86-382C=
ENST00000534011.6:n.1009C=
ENST00000685484.1:c.717C= ENSP00000510622.1:p.Cys239=
ENST00000685601.1:c.717C= ENSP00000510603.1:p.Cys239=
ENST00000685765.1:c.717C= ENSP00000509991.1:p.Cys239=
ENST00000685844.1:c.*254C= ENSP00000509820.1:n.*254C=
ENST00000685857.1:n.1456C=
ENST00000686242.1:c.516C= ENSP00000508950.1:n.516C=
ENST00000686888.1:c.*284C= ENSP00000509619.1:n.*284C=
ENST00000687699.1:c.841C= ENSP00000508878.1:n.841C=
ENST00000687786.1:n.2153C=
ENST00000688100.1:n.1638C=
ENST00000688588.1:c.717C= ENSP00000510802.1:p.Cys239=
ENST00000688927.1:n.2928C=
ENST00000689283.1:c.*380C= ENSP00000509050.1:n.*380C=
ENST00000689477.1:c.*610C= ENSP00000508945.1:n.*610C=
ENST00000689765.1:c.*210C= ENSP00000509625.1:n.*210C=
ENST00000690512.1:c.*568C= ENSP00000509793.1:n.*568C=
ENST00000692039.1:c.*515C= ENSP00000508821.1:n.*515C=
ENST00000692336.1:c.741C= ENSP00000508540.1:p.Cys247=
ENST00000693133.1:n.1197C=
ENST00000263578.10:c.717C= MANE Select ENSP00000263578.5:p.Cys239=
ENST00000263578.9:c.717C= ENSP00000263578.5:p.Cys239=
ENST00000525083.5:n.437C=
ENST00000525770.5:c.*349C= ENSP00000434739.1:n.*349C=
ENST00000527004.5:c.*61C= ENSP00000436374.1:n.*61C=
ENST00000530642.1:n.1499C=
ENST00000532101.5:n.940C=
ENST00000532125.1:c.675C= ENSP00000434178.1:p.Cys225=
ENST00000533395.5:n.450C=
ENST00000533839.5:n.238-382C=
ENST00000534011.5:n.769C=
ENST00000534315.5:n.1029C=
NM_017547.3:c.717C= NP_060017.1:p.Cys239=
NR_037647.1:n.663C=
NR_037648.1:n.903C=
XM_006718879.2:c.207C= XP_006718942.1:p.Cys69=
XM_006718880.2:c.84C= XP_006718943.1:p.Cys28=
XM_006718881.2:c.84C= XP_006718944.1:p.Cys28=
XM_011542895.1:c.207C= XP_011541197.1:p.Cys69=
XM_011542896.1:c.207C= XP_011541198.1:p.Cys69=
XM_006718879.3:c.207C= XP_006718942.1:p.Cys69=
XM_006718881.3:c.84C= XP_006718944.1:p.Cys28=
XM_011542895.2:c.207C= XP_011541197.1:p.Cys69=
XM_011542896.2:c.207C= XP_011541198.1:p.Cys69=
XM_017018000.2:c.717C= XP_016873489.1:p.Cys239=
XM_017018001.1:c.207C= XP_016873490.1:p.Cys69=
XM_017018002.1:c.207C= XP_016873491.1:p.Cys69=
XM_017018003.2:c.84C= XP_016873492.1:p.Cys28=
XM_017018004.1:c.84C= XP_016873493.1:p.Cys28=
XM_017018005.1:c.84C= XP_016873494.1:p.Cys28=
XM_017018006.2:c.84C= XP_016873495.1:p.Cys28=
NM_017547.4:c.717C= MANE Select NP_060017.1:p.Cys239=
NR_037647.2:n.549C=
NR_037648.2:n.894C=