Canonical Allele Identifier: CA2007079598
Gene: FOXRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126275132C= , CM000673.2:g.126275132C= GRCh38
NC_000011.9:g.126145027C= , CM000673.1:g.126145027C= GRCh37
NC_000011.8:g.125650237C= NCBI36
NG_028029.1:g.11093C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.920C=
ENST00000532101.6:n.734-195C=
ENST00000532125.2:c.628+111C= ENSP00000434178.2:n.628+111C=
ENST00000533839.6:c.86-662C= ENSP00000509952.1:n.86-662C=
ENST00000534011.6:n.923+111C=
ENST00000685484.1:c.631+111C= ENSP00000510622.1:n.631+111C=
ENST00000685601.1:c.631+111C= ENSP00000510603.1:n.631+111C=
ENST00000685765.1:c.631+111C= ENSP00000509991.1:n.631+111C=
ENST00000685844.1:c.*169-195C= ENSP00000509820.1:n.*169-195C=
ENST00000685857.1:n.1176C=
ENST00000686242.1:c.430+111C= ENSP00000508950.1:n.430+111C=
ENST00000686888.1:c.*198+111C= ENSP00000509619.1:n.*198+111C=
ENST00000687699.1:c.755+111C= ENSP00000508878.1:n.755+111C=
ENST00000687786.1:n.2068-195C=
ENST00000688100.1:n.1552+111C=
ENST00000688588.1:c.631+111C= ENSP00000510802.1:n.631+111C=
ENST00000688927.1:n.2648C=
ENST00000689283.1:c.*294+111C= ENSP00000509050.1:n.*294+111C=
ENST00000689477.1:c.*524+111C= ENSP00000508945.1:n.*524+111C=
ENST00000689765.1:c.*169-239C= ENSP00000509625.1:n.*169-239C=
ENST00000690512.1:c.*482+111C= ENSP00000509793.1:n.*482+111C=
ENST00000692039.1:c.*429+111C= ENSP00000508821.1:n.*429+111C=
ENST00000692336.1:c.655+111C= ENSP00000508540.1:n.655+111C=
ENST00000693133.1:n.917C=
ENST00000263578.10:c.631+111C= MANE Select ENSP00000263578.5:n.631+111C=
ENST00000263578.9:c.631+111C= ENSP00000263578.5:n.631+111C=
ENST00000524751.5:n.678C=
ENST00000525083.5:n.352-195C=
ENST00000525770.5:c.*263+111C= ENSP00000434739.1:n.*263+111C=
ENST00000527004.5:c.534-195C= ENSP00000436374.1:n.534-195C=
ENST00000527875.1:n.572C=
ENST00000530642.1:n.1219C=
ENST00000532101.5:n.854+111C=
ENST00000532125.1:c.589+111C= ENSP00000434178.1:n.589+111C=
ENST00000533395.5:n.365-195C=
ENST00000533839.5:n.238-662C=
ENST00000534011.5:n.683+111C=
ENST00000534315.5:n.944-195C=
NM_017547.3:c.631+111C= NP_060017.1:n.631+111C=
NR_037647.1:n.577+111C=
NR_037648.1:n.817+111C=
XM_006718879.2:c.121+111C= XP_006718942.1:n.121+111C=
XM_006718880.2:c.-2-195C= XP_006718943.1:n.-2-195C=
XM_006718881.2:c.-2-195C= XP_006718944.1:n.-2-195C=
XM_011542895.1:c.121+111C= XP_011541197.1:n.121+111C=
XM_011542896.1:c.121+111C= XP_011541198.1:n.121+111C=
XM_006718879.3:c.121+111C= XP_006718942.1:n.121+111C=
XM_006718881.3:c.-2-195C= XP_006718944.1:n.-2-195C=
XM_011542895.2:c.121+111C= XP_011541197.1:n.121+111C=
XM_011542896.2:c.121+111C= XP_011541198.1:n.121+111C=
XM_017018000.2:c.631+111C= XP_016873489.1:n.631+111C=
XM_017018001.1:c.121+111C= XP_016873490.1:n.121+111C=
XM_017018002.1:c.121+111C= XP_016873491.1:n.121+111C=
XM_017018003.2:c.-2-195C= XP_016873492.1:n.-2-195C=
XM_017018004.1:c.-2-195C= XP_016873493.1:n.-2-195C=
XM_017018005.1:c.-2-195C= XP_016873494.1:n.-2-195C=
XM_017018006.2:c.-2-195C= XP_016873495.1:n.-2-195C=
NM_017547.4:c.631+111C= MANE Select NP_060017.1:n.631+111C=
NR_037647.2:n.463+111C=
NR_037648.2:n.808+111C=