Canonical Allele Identifier: CA2007079545
Gene: FOXRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126274979T= , CM000673.2:g.126274979T= GRCh38
NC_000011.9:g.126144874T= , CM000673.1:g.126144874T= GRCh37
NC_000011.8:g.125650084T= NCBI36
NG_028029.1:g.10940T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.767T=
ENST00000532101.6:n.734-348T=
ENST00000532125.2:c.586T= ENSP00000434178.2:p.Phe196=
ENST00000533839.6:c.86-815T= ENSP00000509952.1:n.86-815T=
ENST00000534011.6:n.881T=
ENST00000685484.1:c.589T= ENSP00000510622.1:p.Phe197=
ENST00000685601.1:c.589T= ENSP00000510603.1:p.Phe197=
ENST00000685765.1:c.589T= ENSP00000509991.1:p.Phe197=
ENST00000685844.1:c.*169-348T= ENSP00000509820.1:n.*169-348T=
ENST00000685857.1:n.1023T=
ENST00000686242.1:c.388T= ENSP00000508950.1:n.388T=
ENST00000686888.1:c.*156T= ENSP00000509619.1:n.*156T=
ENST00000687699.1:c.713T= ENSP00000508878.1:n.713T=
ENST00000687786.1:n.2068-348T=
ENST00000688100.1:n.1510T=
ENST00000688588.1:c.589T= ENSP00000510802.1:p.Phe197=
ENST00000688927.1:n.2495T=
ENST00000689283.1:c.*252T= ENSP00000509050.1:n.*252T=
ENST00000689477.1:c.*482T= ENSP00000508945.1:n.*482T=
ENST00000689765.1:c.*169-392T= ENSP00000509625.1:n.*169-392T=
ENST00000690512.1:c.*440T= ENSP00000509793.1:n.*440T=
ENST00000692039.1:c.*387T= ENSP00000508821.1:n.*387T=
ENST00000692336.1:c.613T= ENSP00000508540.1:p.Phe205=
ENST00000693133.1:n.764T=
ENST00000263578.10:c.589T= MANE Select ENSP00000263578.5:p.Phe197=
ENST00000263578.9:c.589T= ENSP00000263578.5:p.Phe197=
ENST00000524751.5:n.525T=
ENST00000525083.5:n.352-348T=
ENST00000525770.5:c.*221T= ENSP00000434739.1:n.*221T=
ENST00000526366.5:n.520T=
ENST00000527004.5:c.534-348T= ENSP00000436374.1:n.534-348T=
ENST00000527875.1:n.419T=
ENST00000530642.1:n.1066T=
ENST00000532101.5:n.812T=
ENST00000532125.1:c.547T= ENSP00000434178.1:p.Phe183=
ENST00000533395.5:n.365-348T=
ENST00000533839.5:n.238-815T=
ENST00000534011.5:n.641T=
ENST00000534315.5:n.944-348T=
NM_017547.3:c.589T= NP_060017.1:p.Phe197=
NR_037647.1:n.535T=
NR_037648.1:n.775T=
XM_006718879.2:c.79T= XP_006718942.1:p.Phe27=
XM_006718880.2:c.-2-348T= XP_006718943.1:n.-2-348T=
XM_006718881.2:c.-2-348T= XP_006718944.1:n.-2-348T=
XM_011542895.1:c.79T= XP_011541197.1:p.Phe27=
XM_011542896.1:c.79T= XP_011541198.1:p.Phe27=
XM_006718879.3:c.79T= XP_006718942.1:p.Phe27=
XM_006718881.3:c.-2-348T= XP_006718944.1:n.-2-348T=
XM_011542895.2:c.79T= XP_011541197.1:p.Phe27=
XM_011542896.2:c.79T= XP_011541198.1:p.Phe27=
XM_017018000.2:c.589T= XP_016873489.1:p.Phe197=
XM_017018001.1:c.79T= XP_016873490.1:p.Phe27=
XM_017018002.1:c.79T= XP_016873491.1:p.Phe27=
XM_017018003.2:c.-2-348T= XP_016873492.1:n.-2-348T=
XM_017018004.1:c.-2-348T= XP_016873493.1:n.-2-348T=
XM_017018005.1:c.-2-348T= XP_016873494.1:n.-2-348T=
XM_017018006.2:c.-2-348T= XP_016873495.1:n.-2-348T=
NM_017547.4:c.589T= MANE Select NP_060017.1:p.Phe197=
NR_037647.2:n.421T=
NR_037648.2:n.766T=