Canonical Allele Identifier: CA2575022777
Gene: FOXRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126275413del , CM000673.2:g.126275413del GRCh38
NC_000011.9:g.126145308del , CM000673.1:g.126145308del GRCh37
NC_000011.8:g.125650518del NCBI36
NG_028029.1:g.11374del

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.1201del
ENST00000532101.6:n.820del
ENST00000532125.2:c.715del ENSP00000434178.2:p.Gln239ArgfsTer4
ENST00000533839.6:c.86-381del ENSP00000509952.1:n.86-381del
ENST00000534011.6:n.1010del
ENST00000685484.1:c.718del ENSP00000510622.1:p.Gln240ArgfsTer4
ENST00000685601.1:c.718del ENSP00000510603.1:p.Gln240ArgfsTer4
ENST00000685765.1:c.718del ENSP00000509991.1:p.Gln240ArgfsTer4
ENST00000685844.1:c.*255del ENSP00000509820.1:n.*255del
ENST00000685857.1:n.1457del
ENST00000686242.1:c.517del ENSP00000508950.1:n.517del
ENST00000686888.1:c.*285del ENSP00000509619.1:n.*285del
ENST00000687699.1:c.842del ENSP00000508878.1:n.842del
ENST00000687786.1:n.2154del
ENST00000688100.1:n.1639del
ENST00000688588.1:c.718del ENSP00000510802.1:p.Gln240ArgfsTer4
ENST00000688927.1:n.2929del
ENST00000689283.1:c.*381del ENSP00000509050.1:n.*381del
ENST00000689477.1:c.*611del ENSP00000508945.1:n.*611del
ENST00000689765.1:c.*211del ENSP00000509625.1:n.*211del
ENST00000690512.1:c.*569del ENSP00000509793.1:n.*569del
ENST00000692039.1:c.*516del ENSP00000508821.1:n.*516del
ENST00000692336.1:c.742del ENSP00000508540.1:p.Gln248ArgfsTer4
ENST00000693133.1:n.1198del
ENST00000263578.10:c.718del MANE Select ENSP00000263578.5:p.Gln240ArgfsTer4
ENST00000263578.9:c.718del ENSP00000263578.5:p.Gln240ArgfsTer4
ENST00000525083.5:n.438del
ENST00000525770.5:c.*350del ENSP00000434739.1:n.*350del
ENST00000527004.5:c.*62del ENSP00000436374.1:n.*62del
ENST00000530642.1:n.1500del
ENST00000532101.5:n.941del
ENST00000532125.1:c.676del ENSP00000434178.1:p.Gln226ArgfsTer4
ENST00000533395.5:n.451del
ENST00000533839.5:n.238-381del
ENST00000534011.5:n.770del
ENST00000534315.5:n.1030del
NM_017547.3:c.718del NP_060017.1:p.Gln240ArgfsTer4
NR_037647.1:n.664del
NR_037648.1:n.904del
XM_006718879.2:c.208del XP_006718942.1:p.Gln70ArgfsTer4
XM_006718880.2:c.85del XP_006718943.1:p.Gln29ArgfsTer4
XM_006718881.2:c.85del XP_006718944.1:p.Gln29ArgfsTer4
XM_011542895.1:c.208del XP_011541197.1:p.Gln70ArgfsTer4
XM_011542896.1:c.208del XP_011541198.1:p.Gln70ArgfsTer4
XM_006718879.3:c.208del XP_006718942.1:p.Gln70ArgfsTer4
XM_006718881.3:c.85del XP_006718944.1:p.Gln29ArgfsTer4
XM_011542895.2:c.208del XP_011541197.1:p.Gln70ArgfsTer4
XM_011542896.2:c.208del XP_011541198.1:p.Gln70ArgfsTer4
XM_017018000.2:c.718del XP_016873489.1:p.Gln240ArgfsTer4
XM_017018001.1:c.208del XP_016873490.1:p.Gln70ArgfsTer4
XM_017018002.1:c.208del XP_016873491.1:p.Gln70ArgfsTer4
XM_017018003.2:c.85del XP_016873492.1:p.Gln29ArgfsTer4
XM_017018004.1:c.85del XP_016873493.1:p.Gln29ArgfsTer4
XM_017018005.1:c.85del XP_016873494.1:p.Gln29ArgfsTer4
XM_017018006.2:c.85del XP_016873495.1:p.Gln29ArgfsTer4
NM_017547.4:c.718del MANE Select NP_060017.1:p.Gln240ArgfsTer4
NR_037647.2:n.550del
NR_037648.2:n.895del