Canonical Allele Identifier: CA2007079530
Gene: FOXRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126274941A= , CM000673.2:g.126274941A= GRCh38
NC_000011.9:g.126144836A= , CM000673.1:g.126144836A= GRCh37
NC_000011.8:g.125650046A= NCBI36
NG_028029.1:g.10902A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.729A=
ENST00000532101.6:n.734-386A=
ENST00000532125.2:c.548A= ENSP00000434178.2:p.Lys183=
ENST00000533839.6:c.86-853A= ENSP00000509952.1:n.86-853A=
ENST00000534011.6:n.843A=
ENST00000685484.1:c.551A= ENSP00000510622.1:p.Lys184=
ENST00000685601.1:c.551A= ENSP00000510603.1:p.Lys184=
ENST00000685765.1:c.551A= ENSP00000509991.1:p.Lys184=
ENST00000685844.1:c.*169-386A= ENSP00000509820.1:n.*169-386A=
ENST00000685857.1:n.985A=
ENST00000686242.1:c.350A= ENSP00000508950.1:n.350A=
ENST00000686888.1:c.*118A= ENSP00000509619.1:n.*118A=
ENST00000687699.1:c.675A= ENSP00000508878.1:n.675A=
ENST00000687786.1:n.2068-386A=
ENST00000688100.1:n.1472A=
ENST00000688588.1:c.551A= ENSP00000510802.1:p.Lys184=
ENST00000688927.1:n.2457A=
ENST00000689283.1:c.*214A= ENSP00000509050.1:n.*214A=
ENST00000689477.1:c.*444A= ENSP00000508945.1:n.*444A=
ENST00000689765.1:c.*169-430A= ENSP00000509625.1:n.*169-430A=
ENST00000690512.1:c.*402A= ENSP00000509793.1:n.*402A=
ENST00000692039.1:c.*349A= ENSP00000508821.1:n.*349A=
ENST00000692336.1:c.575A= ENSP00000508540.1:p.Lys192=
ENST00000693133.1:n.726A=
ENST00000263578.10:c.551A= MANE Select ENSP00000263578.5:p.Lys184=
ENST00000263578.9:c.551A= ENSP00000263578.5:p.Lys184=
ENST00000524751.5:n.487A=
ENST00000525083.5:n.352-386A=
ENST00000525770.5:c.*183A= ENSP00000434739.1:n.*183A=
ENST00000526366.5:n.482A=
ENST00000527004.5:c.534-386A= ENSP00000436374.1:n.534-386A=
ENST00000527875.1:n.381A=
ENST00000530642.1:n.1028A=
ENST00000532101.5:n.774A=
ENST00000532125.1:c.509A= ENSP00000434178.1:p.Lys170=
ENST00000533395.5:n.365-386A=
ENST00000533839.5:n.238-853A=
ENST00000534011.5:n.603A=
ENST00000534315.5:n.944-386A=
NM_017547.3:c.551A= NP_060017.1:p.Lys184=
NR_037647.1:n.497A=
NR_037648.1:n.737A=
XM_006718879.2:c.41A= XP_006718942.1:p.Lys14=
XM_006718880.2:c.-2-386A= XP_006718943.1:n.-2-386A=
XM_006718881.2:c.-2-386A= XP_006718944.1:n.-2-386A=
XM_011542895.1:c.41A= XP_011541197.1:p.Lys14=
XM_011542896.1:c.41A= XP_011541198.1:p.Lys14=
XM_006718879.3:c.41A= XP_006718942.1:p.Lys14=
XM_006718881.3:c.-2-386A= XP_006718944.1:n.-2-386A=
XM_011542895.2:c.41A= XP_011541197.1:p.Lys14=
XM_011542896.2:c.41A= XP_011541198.1:p.Lys14=
XM_017018000.2:c.551A= XP_016873489.1:p.Lys184=
XM_017018001.1:c.41A= XP_016873490.1:p.Lys14=
XM_017018002.1:c.41A= XP_016873491.1:p.Lys14=
XM_017018003.2:c.-2-386A= XP_016873492.1:n.-2-386A=
XM_017018004.1:c.-2-386A= XP_016873493.1:n.-2-386A=
XM_017018005.1:c.-2-386A= XP_016873494.1:n.-2-386A=
XM_017018006.2:c.-2-386A= XP_016873495.1:n.-2-386A=
NM_017547.4:c.551A= MANE Select NP_060017.1:p.Lys184=
NR_037647.2:n.383A=
NR_037648.2:n.728A=