Canonical Allele Identifier: CA2616719024
Gene: FOXRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126271561_126271570del , CM000673.2:g.126271561_126271570del GRCh38
NC_000011.9:g.126141456_126141465del , CM000673.1:g.126141456_126141465del GRCh37
NC_000011.8:g.125646666_125646675del NCBI36
NG_028029.1:g.7522_7531del

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.388_397del
ENST00000532101.6:n.387_396del
ENST00000532125.2:c.210_219del ENSP00000434178.2:p.Gly71LeufsTer9
ENST00000533839.6:c.85+2270_85+2279del ENSP00000509952.1:n.85+2270_85+2279del
ENST00000534011.6:n.486_495del
ENST00000685484.1:c.210_219del ENSP00000510622.1:p.Gly71LeufsTer9
ENST00000685601.1:c.210_219del ENSP00000510603.1:p.Gly71LeufsTer9
ENST00000685765.1:c.210_219del ENSP00000509991.1:p.Gly71LeufsTer9
ENST00000685844.1:c.86-1408_86-1399del ENSP00000509820.1:n.86-1408_86-1399del
ENST00000685857.1:n.388_397del
ENST00000686242.1:c.86-1408_86-1399del ENSP00000508950.1:n.86-1408_86-1399del
ENST00000686888.1:c.210_219del ENSP00000509619.1:p.Gly71LeufsTer9
ENST00000687699.1:c.334_343del ENSP00000508878.1:n.334_343del
ENST00000687786.1:n.1543_1552del
ENST00000688588.1:c.210_219del ENSP00000510802.1:p.Gly71LeufsTer9
ENST00000688927.1:n.388_397del
ENST00000689283.1:c.210-1408_210-1399del ENSP00000509050.1:n.210-1408_210-1399del
ENST00000689477.1:c.*103_*112del ENSP00000508945.1:n.*103_*112del
ENST00000689765.1:c.86-1408_86-1399del ENSP00000509625.1:n.86-1408_86-1399del
ENST00000690512.1:c.86-917_86-908del ENSP00000509793.1:n.86-917_86-908del
ENST00000692039.1:c.*8_*17del ENSP00000508821.1:n.*8_*17del
ENST00000692336.1:c.210_219del ENSP00000508540.1:p.Gly71LeufsTer9
ENST00000693133.1:n.226-1408_226-1399del
ENST00000263578.10:c.210_219del MANE Select ENSP00000263578.5:p.Gly71LeufsTer9
ENST00000263578.9:c.210_219del ENSP00000263578.5:p.Gly71LeufsTer9
ENST00000524751.5:n.223-1408_223-1399del
ENST00000525083.5:n.122-1408_122-1399del
ENST00000525770.5:c.86-1408_86-1399del ENSP00000434739.1:n.86-1408_86-1399del
ENST00000526366.5:n.101-158_101-149del
ENST00000526525.1:n.246-1408_246-1399del
ENST00000527004.5:c.210_219del ENSP00000436374.1:p.Gly71LeufsTer9
ENST00000529802.1:n.260_269del
ENST00000532101.5:n.433_442del
ENST00000532125.1:c.168_177del ENSP00000434178.1:p.Gly57LeufsTer9
ENST00000533839.5:n.237+2270_237+2279del
ENST00000534011.5:n.158-917_158-908del
ENST00000534315.5:n.617_626del
NM_017547.3:c.210_219del NP_060017.1:p.Gly71LeufsTer9
NR_037647.1:n.253-1408_253-1399del
NR_037648.1:n.396_405del
XM_006718880.2:c.-329_-320del XP_006718943.1:n.-329_-320del
XM_006718881.2:c.-232-1408_-232-1399del XP_006718944.1:n.-232-1408_-232-1399del
XM_011542895.1:c.-301_-292del XP_011541197.1:n.-301_-292del
XM_011542896.1:c.-321_-312del XP_011541198.1:n.-321_-312del
XM_006718881.3:c.-232-1408_-232-1399del XP_006718944.1:n.-232-1408_-232-1399del
XM_011542895.2:c.-301_-292del XP_011541197.1:n.-301_-292del
XM_011542896.2:c.-321_-312del XP_011541198.1:n.-321_-312del
XM_017018000.2:c.210_219del XP_016873489.1:p.Gly71LeufsTer9
XM_017018001.1:c.-321_-312del XP_016873490.1:n.-321_-312del
XM_017018002.1:c.-224-1408_-224-1399del XP_016873491.1:n.-224-1408_-224-1399del
XM_017018003.2:c.-329_-320del XP_016873492.1:n.-329_-320del
XM_017018004.1:c.-329_-320del XP_016873493.1:n.-329_-320del
XM_017018005.1:c.-527_-518del XP_016873494.1:n.-527_-518del
XM_017018006.2:c.-329_-320del XP_016873495.1:n.-329_-320del
NM_017547.4:c.210_219del MANE Select NP_060017.1:p.Gly71LeufsTer9
NR_037647.2:n.139-1408_139-1399del
NR_037648.2:n.387_396del