Canonical Allele Identifier: CA2007079550
Gene: FOXRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126274990A= , CM000673.2:g.126274990A= GRCh38
NC_000011.9:g.126144885A= , CM000673.1:g.126144885A= GRCh37
NC_000011.8:g.125650095A= NCBI36
NG_028029.1:g.10951A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.778A=
ENST00000532101.6:n.734-337A=
ENST00000532125.2:c.597A= ENSP00000434178.2:p.Ile199=
ENST00000533839.6:c.86-804A= ENSP00000509952.1:n.86-804A=
ENST00000534011.6:n.892A=
ENST00000685484.1:c.600A= ENSP00000510622.1:p.Ile200=
ENST00000685601.1:c.600A= ENSP00000510603.1:p.Ile200=
ENST00000685765.1:c.600A= ENSP00000509991.1:p.Ile200=
ENST00000685844.1:c.*169-337A= ENSP00000509820.1:n.*169-337A=
ENST00000685857.1:n.1034A=
ENST00000686242.1:c.399A= ENSP00000508950.1:n.399A=
ENST00000686888.1:c.*167A= ENSP00000509619.1:n.*167A=
ENST00000687699.1:c.724A= ENSP00000508878.1:n.724A=
ENST00000687786.1:n.2068-337A=
ENST00000688100.1:n.1521A=
ENST00000688588.1:c.600A= ENSP00000510802.1:p.Ile200=
ENST00000688927.1:n.2506A=
ENST00000689283.1:c.*263A= ENSP00000509050.1:n.*263A=
ENST00000689477.1:c.*493A= ENSP00000508945.1:n.*493A=
ENST00000689765.1:c.*169-381A= ENSP00000509625.1:n.*169-381A=
ENST00000690512.1:c.*451A= ENSP00000509793.1:n.*451A=
ENST00000692039.1:c.*398A= ENSP00000508821.1:n.*398A=
ENST00000692336.1:c.624A= ENSP00000508540.1:p.Ile208=
ENST00000693133.1:n.775A=
ENST00000263578.10:c.600A= MANE Select ENSP00000263578.5:p.Ile200=
ENST00000263578.9:c.600A= ENSP00000263578.5:p.Ile200=
ENST00000524751.5:n.536A=
ENST00000525083.5:n.352-337A=
ENST00000525770.5:c.*232A= ENSP00000434739.1:n.*232A=
ENST00000526366.5:n.531A=
ENST00000527004.5:c.534-337A= ENSP00000436374.1:n.534-337A=
ENST00000527875.1:n.430A=
ENST00000530642.1:n.1077A=
ENST00000532101.5:n.823A=
ENST00000532125.1:c.558A= ENSP00000434178.1:p.Ile186=
ENST00000533395.5:n.365-337A=
ENST00000533839.5:n.238-804A=
ENST00000534011.5:n.652A=
ENST00000534315.5:n.944-337A=
NM_017547.3:c.600A= NP_060017.1:p.Ile200=
NR_037647.1:n.546A=
NR_037648.1:n.786A=
XM_006718879.2:c.90A= XP_006718942.1:p.Ile30=
XM_006718880.2:c.-2-337A= XP_006718943.1:n.-2-337A=
XM_006718881.2:c.-2-337A= XP_006718944.1:n.-2-337A=
XM_011542895.1:c.90A= XP_011541197.1:p.Ile30=
XM_011542896.1:c.90A= XP_011541198.1:p.Ile30=
XM_006718879.3:c.90A= XP_006718942.1:p.Ile30=
XM_006718881.3:c.-2-337A= XP_006718944.1:n.-2-337A=
XM_011542895.2:c.90A= XP_011541197.1:p.Ile30=
XM_011542896.2:c.90A= XP_011541198.1:p.Ile30=
XM_017018000.2:c.600A= XP_016873489.1:p.Ile200=
XM_017018001.1:c.90A= XP_016873490.1:p.Ile30=
XM_017018002.1:c.90A= XP_016873491.1:p.Ile30=
XM_017018003.2:c.-2-337A= XP_016873492.1:n.-2-337A=
XM_017018004.1:c.-2-337A= XP_016873493.1:n.-2-337A=
XM_017018005.1:c.-2-337A= XP_016873494.1:n.-2-337A=
XM_017018006.2:c.-2-337A= XP_016873495.1:n.-2-337A=
NM_017547.4:c.600A= MANE Select NP_060017.1:p.Ile200=
NR_037647.2:n.432A=
NR_037648.2:n.777A=