Canonical Allele Identifier: CA2616722199
Gene: FOXRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126274961del , CM000673.2:g.126274961del GRCh38
NC_000011.9:g.126144856del , CM000673.1:g.126144856del GRCh37
NC_000011.8:g.125650066del NCBI36
NG_028029.1:g.10922del

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.749del
ENST00000532101.6:n.734-366del
ENST00000532125.2:c.568del ENSP00000434178.2:p.Asp190IlefsTer10
ENST00000533839.6:c.86-833del ENSP00000509952.1:n.86-833del
ENST00000534011.6:n.863del
ENST00000685484.1:c.571del ENSP00000510622.1:p.Asp191IlefsTer10
ENST00000685601.1:c.571del ENSP00000510603.1:p.Asp191IlefsTer10
ENST00000685765.1:c.571del ENSP00000509991.1:p.Asp191IlefsTer10
ENST00000685844.1:c.*169-366del ENSP00000509820.1:n.*169-366del
ENST00000685857.1:n.1005del
ENST00000686242.1:c.370del ENSP00000508950.1:n.370del
ENST00000686888.1:c.*138del ENSP00000509619.1:n.*138del
ENST00000687699.1:c.695del ENSP00000508878.1:n.695del
ENST00000687786.1:n.2068-366del
ENST00000688100.1:n.1492del
ENST00000688588.1:c.571del ENSP00000510802.1:p.Asp191IlefsTer10
ENST00000688927.1:n.2477del
ENST00000689283.1:c.*234del ENSP00000509050.1:n.*234del
ENST00000689477.1:c.*464del ENSP00000508945.1:n.*464del
ENST00000689765.1:c.*169-410del ENSP00000509625.1:n.*169-410del
ENST00000690512.1:c.*422del ENSP00000509793.1:n.*422del
ENST00000692039.1:c.*369del ENSP00000508821.1:n.*369del
ENST00000692336.1:c.595del ENSP00000508540.1:p.Asp199IlefsTer10
ENST00000693133.1:n.746del
ENST00000263578.10:c.571del MANE Select ENSP00000263578.5:p.Asp191IlefsTer10
ENST00000263578.9:c.571del ENSP00000263578.5:p.Asp191IlefsTer10
ENST00000524751.5:n.507del
ENST00000525083.5:n.352-366del
ENST00000525770.5:c.*203del ENSP00000434739.1:n.*203del
ENST00000526366.5:n.502del
ENST00000527004.5:c.534-366del ENSP00000436374.1:n.534-366del
ENST00000527875.1:n.401del
ENST00000530642.1:n.1048del
ENST00000532101.5:n.794del
ENST00000532125.1:c.529del ENSP00000434178.1:p.Asp177IlefsTer10
ENST00000533395.5:n.365-366del
ENST00000533839.5:n.238-833del
ENST00000534011.5:n.623del
ENST00000534315.5:n.944-366del
NM_017547.3:c.571del NP_060017.1:p.Asp191IlefsTer10
NR_037647.1:n.517del
NR_037648.1:n.757del
XM_006718879.2:c.61del XP_006718942.1:p.Asp21IlefsTer10
XM_006718880.2:c.-2-366del XP_006718943.1:n.-2-366del
XM_006718881.2:c.-2-366del XP_006718944.1:n.-2-366del
XM_011542895.1:c.61del XP_011541197.1:p.Asp21IlefsTer10
XM_011542896.1:c.61del XP_011541198.1:p.Asp21IlefsTer10
XM_006718879.3:c.61del XP_006718942.1:p.Asp21IlefsTer10
XM_006718881.3:c.-2-366del XP_006718944.1:n.-2-366del
XM_011542895.2:c.61del XP_011541197.1:p.Asp21IlefsTer10
XM_011542896.2:c.61del XP_011541198.1:p.Asp21IlefsTer10
XM_017018000.2:c.571del XP_016873489.1:p.Asp191IlefsTer10
XM_017018001.1:c.61del XP_016873490.1:p.Asp21IlefsTer10
XM_017018002.1:c.61del XP_016873491.1:p.Asp21IlefsTer10
XM_017018003.2:c.-2-366del XP_016873492.1:n.-2-366del
XM_017018004.1:c.-2-366del XP_016873493.1:n.-2-366del
XM_017018005.1:c.-2-366del XP_016873494.1:n.-2-366del
XM_017018006.2:c.-2-366del XP_016873495.1:n.-2-366del
NM_017547.4:c.571del MANE Select NP_060017.1:p.Asp191IlefsTer10
NR_037647.2:n.403del
NR_037648.2:n.748del