Canonical Allele Identifier: CA2007079520
Gene: FOXRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126274920A= , CM000673.2:g.126274920A= GRCh38
NC_000011.9:g.126144815A= , CM000673.1:g.126144815A= GRCh37
NC_000011.8:g.125650025A= NCBI36
NG_028029.1:g.10881A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.715-7A=
ENST00000532101.6:n.734-407A=
ENST00000532125.2:c.534-7A= ENSP00000434178.2:n.534-7A=
ENST00000533839.6:c.86-874A= ENSP00000509952.1:n.86-874A=
ENST00000534011.6:n.833-11A=
ENST00000685484.1:c.537-7A= ENSP00000510622.1:n.537-7A=
ENST00000685601.1:c.537-7A= ENSP00000510603.1:n.537-7A=
ENST00000685765.1:c.537-7A= ENSP00000509991.1:n.537-7A=
ENST00000685844.1:c.*169-407A= ENSP00000509820.1:n.*169-407A=
ENST00000685857.1:n.971-7A=
ENST00000686242.1:c.336-7A= ENSP00000508950.1:n.336-7A=
ENST00000686888.1:c.*104-7A= ENSP00000509619.1:n.*104-7A=
ENST00000687699.1:c.661-7A= ENSP00000508878.1:n.661-7A=
ENST00000687786.1:n.2068-407A=
ENST00000688100.1:n.1458-7A=
ENST00000688588.1:c.537-7A= ENSP00000510802.1:n.537-7A=
ENST00000688927.1:n.2436A=
ENST00000689283.1:c.*200-7A= ENSP00000509050.1:n.*200-7A=
ENST00000689477.1:c.*430-7A= ENSP00000508945.1:n.*430-7A=
ENST00000689765.1:c.*169-451A= ENSP00000509625.1:n.*169-451A=
ENST00000690512.1:c.*392-11A= ENSP00000509793.1:n.*392-11A=
ENST00000692039.1:c.*335-7A= ENSP00000508821.1:n.*335-7A=
ENST00000692336.1:c.561-7A= ENSP00000508540.1:n.561-7A=
ENST00000693133.1:n.712-7A=
ENST00000263578.10:c.537-7A= MANE Select ENSP00000263578.5:n.537-7A=
ENST00000263578.9:c.537-7A= ENSP00000263578.5:n.537-7A=
ENST00000524751.5:n.473-7A=
ENST00000525083.5:n.352-407A=
ENST00000525770.5:c.*169-7A= ENSP00000434739.1:n.*169-7A=
ENST00000526366.5:n.468-7A=
ENST00000527004.5:c.534-407A= ENSP00000436374.1:n.534-407A=
ENST00000527875.1:n.367-7A=
ENST00000530642.1:n.1007A=
ENST00000532101.5:n.760-7A=
ENST00000532125.1:c.495-7A= ENSP00000434178.1:n.495-7A=
ENST00000533395.5:n.365-407A=
ENST00000533839.5:n.238-874A=
ENST00000534011.5:n.593-11A=
ENST00000534315.5:n.944-407A=
NM_017547.3:c.537-7A= NP_060017.1:n.537-7A=
NR_037647.1:n.483-7A=
NR_037648.1:n.723-7A=
XM_006718879.2:c.27-7A= XP_006718942.1:n.27-7A=
XM_006718880.2:c.-2-407A= XP_006718943.1:n.-2-407A=
XM_006718881.2:c.-2-407A= XP_006718944.1:n.-2-407A=
XM_011542895.1:c.27-7A= XP_011541197.1:n.27-7A=
XM_011542896.1:c.27-7A= XP_011541198.1:n.27-7A=
XM_006718879.3:c.27-7A= XP_006718942.1:n.27-7A=
XM_006718881.3:c.-2-407A= XP_006718944.1:n.-2-407A=
XM_011542895.2:c.27-7A= XP_011541197.1:n.27-7A=
XM_011542896.2:c.27-7A= XP_011541198.1:n.27-7A=
XM_017018000.2:c.537-7A= XP_016873489.1:n.537-7A=
XM_017018001.1:c.27-7A= XP_016873490.1:n.27-7A=
XM_017018002.1:c.27-7A= XP_016873491.1:n.27-7A=
XM_017018003.2:c.-2-407A= XP_016873492.1:n.-2-407A=
XM_017018004.1:c.-2-407A= XP_016873493.1:n.-2-407A=
XM_017018005.1:c.-2-407A= XP_016873494.1:n.-2-407A=
XM_017018006.2:c.-2-407A= XP_016873495.1:n.-2-407A=
NM_017547.4:c.537-7A= MANE Select NP_060017.1:n.537-7A=
NR_037647.2:n.369-7A=
NR_037648.2:n.714-7A=