Canonical Allele Identifier: CA2007079560
Gene: FOXRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126275014G= , CM000673.2:g.126275014G= GRCh38
NC_000011.9:g.126144909G= , CM000673.1:g.126144909G= GRCh37
NC_000011.8:g.125650119G= NCBI36
NG_028029.1:g.10975G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.802G=
ENST00000532101.6:n.734-313G=
ENST00000532125.2:c.621G= ENSP00000434178.2:p.Ala207=
ENST00000533839.6:c.86-780G= ENSP00000509952.1:n.86-780G=
ENST00000534011.6:n.916G=
ENST00000685484.1:c.624G= ENSP00000510622.1:p.Ala208=
ENST00000685601.1:c.624G= ENSP00000510603.1:p.Ala208=
ENST00000685765.1:c.624G= ENSP00000509991.1:p.Ala208=
ENST00000685844.1:c.*169-313G= ENSP00000509820.1:n.*169-313G=
ENST00000685857.1:n.1058G=
ENST00000686242.1:c.423G= ENSP00000508950.1:n.423G=
ENST00000686888.1:c.*191G= ENSP00000509619.1:n.*191G=
ENST00000687699.1:c.748G= ENSP00000508878.1:n.748G=
ENST00000687786.1:n.2068-313G=
ENST00000688100.1:n.1545G=
ENST00000688588.1:c.624G= ENSP00000510802.1:p.Ala208=
ENST00000688927.1:n.2530G=
ENST00000689283.1:c.*287G= ENSP00000509050.1:n.*287G=
ENST00000689477.1:c.*517G= ENSP00000508945.1:n.*517G=
ENST00000689765.1:c.*169-357G= ENSP00000509625.1:n.*169-357G=
ENST00000690512.1:c.*475G= ENSP00000509793.1:n.*475G=
ENST00000692039.1:c.*422G= ENSP00000508821.1:n.*422G=
ENST00000692336.1:c.648G= ENSP00000508540.1:p.Ala216=
ENST00000693133.1:n.799G=
ENST00000263578.10:c.624G= MANE Select ENSP00000263578.5:p.Ala208=
ENST00000263578.9:c.624G= ENSP00000263578.5:p.Ala208=
ENST00000524751.5:n.560G=
ENST00000525083.5:n.352-313G=
ENST00000525770.5:c.*256G= ENSP00000434739.1:n.*256G=
ENST00000527004.5:c.534-313G= ENSP00000436374.1:n.534-313G=
ENST00000527875.1:n.454G=
ENST00000530642.1:n.1101G=
ENST00000532101.5:n.847G=
ENST00000532125.1:c.582G= ENSP00000434178.1:p.Ala194=
ENST00000533395.5:n.365-313G=
ENST00000533839.5:n.238-780G=
ENST00000534011.5:n.676G=
ENST00000534315.5:n.944-313G=
NM_017547.3:c.624G= NP_060017.1:p.Ala208=
NR_037647.1:n.570G=
NR_037648.1:n.810G=
XM_006718879.2:c.114G= XP_006718942.1:p.Ala38=
XM_006718880.2:c.-2-313G= XP_006718943.1:n.-2-313G=
XM_006718881.2:c.-2-313G= XP_006718944.1:n.-2-313G=
XM_011542895.1:c.114G= XP_011541197.1:p.Ala38=
XM_011542896.1:c.114G= XP_011541198.1:p.Ala38=
XM_006718879.3:c.114G= XP_006718942.1:p.Ala38=
XM_006718881.3:c.-2-313G= XP_006718944.1:n.-2-313G=
XM_011542895.2:c.114G= XP_011541197.1:p.Ala38=
XM_011542896.2:c.114G= XP_011541198.1:p.Ala38=
XM_017018000.2:c.624G= XP_016873489.1:p.Ala208=
XM_017018001.1:c.114G= XP_016873490.1:p.Ala38=
XM_017018002.1:c.114G= XP_016873491.1:p.Ala38=
XM_017018003.2:c.-2-313G= XP_016873492.1:n.-2-313G=
XM_017018004.1:c.-2-313G= XP_016873493.1:n.-2-313G=
XM_017018005.1:c.-2-313G= XP_016873494.1:n.-2-313G=
XM_017018006.2:c.-2-313G= XP_016873495.1:n.-2-313G=
NM_017547.4:c.624G= MANE Select NP_060017.1:p.Ala208=
NR_037647.2:n.456G=
NR_037648.2:n.801G=