Canonical Allele Identifier: CA2007079524
Gene: FOXRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126274928C= , CM000673.2:g.126274928C= GRCh38
NC_000011.9:g.126144823C= , CM000673.1:g.126144823C= GRCh37
NC_000011.8:g.125650033C= NCBI36
NG_028029.1:g.10889C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.716C=
ENST00000532101.6:n.734-399C=
ENST00000532125.2:c.535C= ENSP00000434178.2:p.Gln179=
ENST00000533839.6:c.86-866C= ENSP00000509952.1:n.86-866C=
ENST00000534011.6:n.833-3C=
ENST00000685484.1:c.538C= ENSP00000510622.1:p.Gln180=
ENST00000685601.1:c.538C= ENSP00000510603.1:p.Gln180=
ENST00000685765.1:c.538C= ENSP00000509991.1:p.Gln180=
ENST00000685844.1:c.*169-399C= ENSP00000509820.1:n.*169-399C=
ENST00000685857.1:n.972C=
ENST00000686242.1:c.337C= ENSP00000508950.1:n.337C=
ENST00000686888.1:c.*105C= ENSP00000509619.1:n.*105C=
ENST00000687699.1:c.662C= ENSP00000508878.1:n.662C=
ENST00000687786.1:n.2068-399C=
ENST00000688100.1:n.1459C=
ENST00000688588.1:c.538C= ENSP00000510802.1:p.Gln180=
ENST00000688927.1:n.2444C=
ENST00000689283.1:c.*201C= ENSP00000509050.1:n.*201C=
ENST00000689477.1:c.*431C= ENSP00000508945.1:n.*431C=
ENST00000689765.1:c.*169-443C= ENSP00000509625.1:n.*169-443C=
ENST00000690512.1:c.*392-3C= ENSP00000509793.1:n.*392-3C=
ENST00000692039.1:c.*336C= ENSP00000508821.1:n.*336C=
ENST00000692336.1:c.562C= ENSP00000508540.1:p.Gln188=
ENST00000693133.1:n.713C=
ENST00000263578.10:c.538C= MANE Select ENSP00000263578.5:p.Gln180=
ENST00000263578.9:c.538C= ENSP00000263578.5:p.Gln180=
ENST00000524751.5:n.474C=
ENST00000525083.5:n.352-399C=
ENST00000525770.5:c.*170C= ENSP00000434739.1:n.*170C=
ENST00000526366.5:n.469C=
ENST00000527004.5:c.534-399C= ENSP00000436374.1:n.534-399C=
ENST00000527875.1:n.368C=
ENST00000530642.1:n.1015C=
ENST00000532101.5:n.761C=
ENST00000532125.1:c.496C= ENSP00000434178.1:p.Gln166=
ENST00000533395.5:n.365-399C=
ENST00000533839.5:n.238-866C=
ENST00000534011.5:n.593-3C=
ENST00000534315.5:n.944-399C=
NM_017547.3:c.538C= NP_060017.1:p.Gln180=
NR_037647.1:n.484C=
NR_037648.1:n.724C=
XM_006718879.2:c.28C= XP_006718942.1:p.Gln10=
XM_006718880.2:c.-2-399C= XP_006718943.1:n.-2-399C=
XM_006718881.2:c.-2-399C= XP_006718944.1:n.-2-399C=
XM_011542895.1:c.28C= XP_011541197.1:p.Gln10=
XM_011542896.1:c.28C= XP_011541198.1:p.Gln10=
XM_006718879.3:c.28C= XP_006718942.1:p.Gln10=
XM_006718881.3:c.-2-399C= XP_006718944.1:n.-2-399C=
XM_011542895.2:c.28C= XP_011541197.1:p.Gln10=
XM_011542896.2:c.28C= XP_011541198.1:p.Gln10=
XM_017018000.2:c.538C= XP_016873489.1:p.Gln180=
XM_017018001.1:c.28C= XP_016873490.1:p.Gln10=
XM_017018002.1:c.28C= XP_016873491.1:p.Gln10=
XM_017018003.2:c.-2-399C= XP_016873492.1:n.-2-399C=
XM_017018004.1:c.-2-399C= XP_016873493.1:n.-2-399C=
XM_017018005.1:c.-2-399C= XP_016873494.1:n.-2-399C=
XM_017018006.2:c.-2-399C= XP_016873495.1:n.-2-399C=
NM_017547.4:c.538C= MANE Select NP_060017.1:p.Gln180=
NR_037647.2:n.370C=
NR_037648.2:n.715C=