Canonical Allele Identifier: CA602355400
Gene: FOXRED1 HGNC NCBI

Linked Data

dbSNP Id: rs1174118804

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126275428del , CM000673.2:g.126275428del GRCh38
NC_000011.9:g.126145323del , CM000673.1:g.126145323del GRCh37
NC_000011.8:g.125650533del NCBI36
NG_028029.1:g.11389del

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.1216del
ENST00000532101.6:n.835del
ENST00000532125.2:c.730del ENSP00000434178.2:p.Arg244ValfsTer10
ENST00000533839.6:c.86-366del ENSP00000509952.1:n.86-366del
ENST00000534011.6:n.1025del
ENST00000685484.1:c.733del ENSP00000510622.1:p.Arg245ValfsTer10
ENST00000685601.1:c.733del ENSP00000510603.1:p.Arg245ValfsTer10
ENST00000685765.1:c.733del ENSP00000509991.1:p.Arg245ValfsTer10
ENST00000685844.1:c.*270del ENSP00000509820.1:n.*270del
ENST00000685857.1:n.1472del
ENST00000686242.1:c.532del ENSP00000508950.1:n.532del
ENST00000686888.1:c.*300del ENSP00000509619.1:n.*300del
ENST00000687699.1:c.857del ENSP00000508878.1:n.857del
ENST00000687786.1:n.2169del
ENST00000688100.1:n.1654del
ENST00000688588.1:c.733del ENSP00000510802.1:p.Arg245ValfsTer10
ENST00000688927.1:n.2944del
ENST00000689283.1:c.*396del ENSP00000509050.1:n.*396del
ENST00000689477.1:c.*626del ENSP00000508945.1:n.*626del
ENST00000689765.1:c.*226del ENSP00000509625.1:n.*226del
ENST00000690512.1:c.*584del ENSP00000509793.1:n.*584del
ENST00000692039.1:c.*531del ENSP00000508821.1:n.*531del
ENST00000692336.1:c.757del ENSP00000508540.1:p.Arg253ValfsTer10
ENST00000693133.1:n.1213del
ENST00000263578.10:c.733del MANE Select ENSP00000263578.5:p.Arg245ValfsTer10
ENST00000263578.9:c.733del ENSP00000263578.5:p.Arg245ValfsTer10
ENST00000525083.5:n.453del
ENST00000525770.5:c.*365del ENSP00000434739.1:n.*365del
ENST00000527004.5:c.*77del ENSP00000436374.1:n.*77del
ENST00000530642.1:n.1515del
ENST00000532101.5:n.956del
ENST00000532125.1:c.691del ENSP00000434178.1:p.Arg231ValfsTer10
ENST00000533395.5:n.466del
ENST00000533839.5:n.238-366del
ENST00000534011.5:n.785del
ENST00000534315.5:n.1045del
NM_017547.3:c.733del NP_060017.1:p.Arg245ValfsTer10
NR_037647.1:n.679del
NR_037648.1:n.919del
XM_006718879.2:c.223del XP_006718942.1:p.Arg75ValfsTer10
XM_006718880.2:c.100del XP_006718943.1:p.Arg34ValfsTer10
XM_006718881.2:c.100del XP_006718944.1:p.Arg34ValfsTer10
XM_011542895.1:c.223del XP_011541197.1:p.Arg75ValfsTer10
XM_011542896.1:c.223del XP_011541198.1:p.Arg75ValfsTer10
XM_006718879.3:c.223del XP_006718942.1:p.Arg75ValfsTer10
XM_006718881.3:c.100del XP_006718944.1:p.Arg34ValfsTer10
XM_011542895.2:c.223del XP_011541197.1:p.Arg75ValfsTer10
XM_011542896.2:c.223del XP_011541198.1:p.Arg75ValfsTer10
XM_017018000.2:c.733del XP_016873489.1:p.Arg245ValfsTer10
XM_017018001.1:c.223del XP_016873490.1:p.Arg75ValfsTer10
XM_017018002.1:c.223del XP_016873491.1:p.Arg75ValfsTer10
XM_017018003.2:c.100del XP_016873492.1:p.Arg34ValfsTer10
XM_017018004.1:c.100del XP_016873493.1:p.Arg34ValfsTer10
XM_017018005.1:c.100del XP_016873494.1:p.Arg34ValfsTer10
XM_017018006.2:c.100del XP_016873495.1:p.Arg34ValfsTer10
NM_017547.4:c.733del MANE Select NP_060017.1:p.Arg245ValfsTer10
NR_037647.2:n.565del
NR_037648.2:n.910del