Canonical Allele Identifier: CA6354000
Gene: FOXRED1 HGNC NCBI

Linked Data

dbSNP Id: rs760592913

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126271553_126271565del , CM000673.2:g.126271553_126271565del GRCh38
NC_000011.9:g.126141448_126141460del , CM000673.1:g.126141448_126141460del GRCh37
NC_000011.8:g.125646658_125646670del NCBI36
NG_028029.1:g.7514_7526del

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.380_392del
ENST00000532101.6:n.379_391del
ENST00000532125.2:c.202_214del ENSP00000434178.2:p.Ile68GlyfsTer11
ENST00000533839.6:c.85+2262_85+2274del ENSP00000509952.1:n.85+2262_85+2274del
ENST00000534011.6:n.478_490del
ENST00000685484.1:c.202_214del ENSP00000510622.1:p.Ile68GlyfsTer11
ENST00000685601.1:c.202_214del ENSP00000510603.1:p.Ile68GlyfsTer11
ENST00000685765.1:c.202_214del ENSP00000509991.1:p.Ile68GlyfsTer11
ENST00000685844.1:c.86-1416_86-1404del ENSP00000509820.1:n.86-1416_86-1404del
ENST00000685857.1:n.380_392del
ENST00000686242.1:c.86-1416_86-1404del ENSP00000508950.1:n.86-1416_86-1404del
ENST00000686888.1:c.202_214del ENSP00000509619.1:p.Ile68GlyfsTer11
ENST00000687699.1:c.326_338del ENSP00000508878.1:n.326_338del
ENST00000687786.1:n.1535_1547del
ENST00000688588.1:c.202_214del ENSP00000510802.1:p.Ile68GlyfsTer11
ENST00000688927.1:n.380_392del
ENST00000689283.1:c.210-1416_210-1404del ENSP00000509050.1:n.210-1416_210-1404del
ENST00000689477.1:c.*95_*107del ENSP00000508945.1:n.*95_*107del
ENST00000689765.1:c.86-1416_86-1404del ENSP00000509625.1:n.86-1416_86-1404del
ENST00000690512.1:c.86-925_86-913del ENSP00000509793.1:n.86-925_86-913del
ENST00000692039.1:c.288_*12del ENSP00000508821.1:n.[c.288_*12del;Ter96TrpextTer?]
ENST00000692336.1:c.202_214del ENSP00000508540.1:p.Ile68GlyfsTer11
ENST00000693133.1:n.226-1416_226-1404del
ENST00000263578.10:c.202_214del MANE Select ENSP00000263578.5:p.Ile68GlyfsTer11
ENST00000263578.9:c.202_214del ENSP00000263578.5:p.Ile68GlyfsTer11
ENST00000524751.5:n.223-1416_223-1404del
ENST00000525083.5:n.122-1416_122-1404del
ENST00000525770.5:c.86-1416_86-1404del ENSP00000434739.1:n.86-1416_86-1404del
ENST00000526366.5:n.101-166_101-154del
ENST00000526525.1:n.246-1416_246-1404del
ENST00000527004.5:c.202_214del ENSP00000436374.1:p.Ile68GlyfsTer11
ENST00000529802.1:n.252_264del
ENST00000532101.5:n.425_437del
ENST00000532125.1:c.160_172del ENSP00000434178.1:p.Ile54GlyfsTer11
ENST00000533839.5:n.237+2262_237+2274del
ENST00000534011.5:n.158-925_158-913del
ENST00000534315.5:n.609_621del
NM_017547.3:c.202_214del NP_060017.1:p.Ile68GlyfsTer11
NR_037647.1:n.253-1416_253-1404del
NR_037648.1:n.388_400del
XM_006718880.2:c.-337_-325del XP_006718943.1:n.-337_-325del
XM_006718881.2:c.-232-1416_-232-1404del XP_006718944.1:n.-232-1416_-232-1404del
XM_011542895.1:c.-309_-297del XP_011541197.1:n.-309_-297del
XM_011542896.1:c.-329_-317del XP_011541198.1:n.-329_-317del
XM_006718881.3:c.-232-1416_-232-1404del XP_006718944.1:n.-232-1416_-232-1404del
XM_011542895.2:c.-309_-297del XP_011541197.1:n.-309_-297del
XM_011542896.2:c.-329_-317del XP_011541198.1:n.-329_-317del
XM_017018000.2:c.202_214del XP_016873489.1:p.Ile68GlyfsTer11
XM_017018001.1:c.-329_-317del XP_016873490.1:n.-329_-317del
XM_017018002.1:c.-224-1416_-224-1404del XP_016873491.1:n.-224-1416_-224-1404del
XM_017018003.2:c.-337_-325del XP_016873492.1:n.-337_-325del
XM_017018004.1:c.-337_-325del XP_016873493.1:n.-337_-325del
XM_017018005.1:c.-535_-523del XP_016873494.1:n.-535_-523del
XM_017018006.2:c.-337_-325del XP_016873495.1:n.-337_-325del
NM_017547.4:c.202_214del MANE Select NP_060017.1:p.Ile68GlyfsTer11
NR_037647.2:n.139-1416_139-1404del
NR_037648.2:n.379_391del