Canonical Allele Identifier: CA2007079546
Gene: FOXRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126274983C= , CM000673.2:g.126274983C= GRCh38
NC_000011.9:g.126144878C= , CM000673.1:g.126144878C= GRCh37
NC_000011.8:g.125650088C= NCBI36
NG_028029.1:g.10944C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.771C=
ENST00000532101.6:n.734-344C=
ENST00000532125.2:c.590C= ENSP00000434178.2:p.Pro197=
ENST00000533839.6:c.86-811C= ENSP00000509952.1:n.86-811C=
ENST00000534011.6:n.885C=
ENST00000685484.1:c.593C= ENSP00000510622.1:p.Pro198=
ENST00000685601.1:c.593C= ENSP00000510603.1:p.Pro198=
ENST00000685765.1:c.593C= ENSP00000509991.1:p.Pro198=
ENST00000685844.1:c.*169-344C= ENSP00000509820.1:n.*169-344C=
ENST00000685857.1:n.1027C=
ENST00000686242.1:c.392C= ENSP00000508950.1:n.392C=
ENST00000686888.1:c.*160C= ENSP00000509619.1:n.*160C=
ENST00000687699.1:c.717C= ENSP00000508878.1:n.717C=
ENST00000687786.1:n.2068-344C=
ENST00000688100.1:n.1514C=
ENST00000688588.1:c.593C= ENSP00000510802.1:p.Pro198=
ENST00000688927.1:n.2499C=
ENST00000689283.1:c.*256C= ENSP00000509050.1:n.*256C=
ENST00000689477.1:c.*486C= ENSP00000508945.1:n.*486C=
ENST00000689765.1:c.*169-388C= ENSP00000509625.1:n.*169-388C=
ENST00000690512.1:c.*444C= ENSP00000509793.1:n.*444C=
ENST00000692039.1:c.*391C= ENSP00000508821.1:n.*391C=
ENST00000692336.1:c.617C= ENSP00000508540.1:p.Pro206=
ENST00000693133.1:n.768C=
ENST00000263578.10:c.593C= MANE Select ENSP00000263578.5:p.Pro198=
ENST00000263578.9:c.593C= ENSP00000263578.5:p.Pro198=
ENST00000524751.5:n.529C=
ENST00000525083.5:n.352-344C=
ENST00000525770.5:c.*225C= ENSP00000434739.1:n.*225C=
ENST00000526366.5:n.524C=
ENST00000527004.5:c.534-344C= ENSP00000436374.1:n.534-344C=
ENST00000527875.1:n.423C=
ENST00000530642.1:n.1070C=
ENST00000532101.5:n.816C=
ENST00000532125.1:c.551C= ENSP00000434178.1:p.Pro184=
ENST00000533395.5:n.365-344C=
ENST00000533839.5:n.238-811C=
ENST00000534011.5:n.645C=
ENST00000534315.5:n.944-344C=
NM_017547.3:c.593C= NP_060017.1:p.Pro198=
NR_037647.1:n.539C=
NR_037648.1:n.779C=
XM_006718879.2:c.83C= XP_006718942.1:p.Pro28=
XM_006718880.2:c.-2-344C= XP_006718943.1:n.-2-344C=
XM_006718881.2:c.-2-344C= XP_006718944.1:n.-2-344C=
XM_011542895.1:c.83C= XP_011541197.1:p.Pro28=
XM_011542896.1:c.83C= XP_011541198.1:p.Pro28=
XM_006718879.3:c.83C= XP_006718942.1:p.Pro28=
XM_006718881.3:c.-2-344C= XP_006718944.1:n.-2-344C=
XM_011542895.2:c.83C= XP_011541197.1:p.Pro28=
XM_011542896.2:c.83C= XP_011541198.1:p.Pro28=
XM_017018000.2:c.593C= XP_016873489.1:p.Pro198=
XM_017018001.1:c.83C= XP_016873490.1:p.Pro28=
XM_017018002.1:c.83C= XP_016873491.1:p.Pro28=
XM_017018003.2:c.-2-344C= XP_016873492.1:n.-2-344C=
XM_017018004.1:c.-2-344C= XP_016873493.1:n.-2-344C=
XM_017018005.1:c.-2-344C= XP_016873494.1:n.-2-344C=
XM_017018006.2:c.-2-344C= XP_016873495.1:n.-2-344C=
NM_017547.4:c.593C= MANE Select NP_060017.1:p.Pro198=
NR_037647.2:n.425C=
NR_037648.2:n.770C=