Canonical Allele Identifier: CA2007079651
Gene: FOXRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126275248_126275252delinsGGGTT , CM000673.2:g.126275248_126275252delinsGGGTT GRCh38
NC_000011.9:g.126145143_126145147delinsGGGTT , CM000673.1:g.126145143_126145147delinsGGGTT GRCh37
NC_000011.8:g.125650353_125650357delinsGGGTT NCBI36
NG_028029.1:g.11209_11213delinsGGGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.1036_1040delinsGGGTT
ENST00000532101.6:n.734-79_734-75delinsGGGTT
ENST00000532125.2:c.629-79_629-75delinsGGGTT ENSP00000434178.2:n.629-79_629-75delinsGGGTT
ENST00000533839.6:c.86-546_86-542delinsGGGTT ENSP00000509952.1:n.86-546_86-542delinsGGGTT
ENST00000534011.6:n.924-79_924-75delinsGGGTT
ENST00000685484.1:c.632-79_632-75delinsGGGTT ENSP00000510622.1:n.632-79_632-75delinsGGGTT
ENST00000685601.1:c.632-79_632-75delinsGGGTT ENSP00000510603.1:n.632-79_632-75delinsGGGTT
ENST00000685765.1:c.632-79_632-75delinsGGGTT ENSP00000509991.1:n.632-79_632-75delinsGGGTT
ENST00000685844.1:c.*169-79_*169-75delinsGGGTT ENSP00000509820.1:n.*169-79_*169-75delinsGGGTT
ENST00000685857.1:n.1292_1296delinsGGGTT
ENST00000686242.1:c.431-79_431-75delinsGGGTT ENSP00000508950.1:n.431-79_431-75delinsGGGTT
ENST00000686888.1:c.*199-79_*199-75delinsGGGTT ENSP00000509619.1:n.*199-79_*199-75delinsGGGTT
ENST00000687699.1:c.756-79_756-75delinsGGGTT ENSP00000508878.1:n.756-79_756-75delinsGGGTT
ENST00000687786.1:n.2068-79_2068-75delinsGGGTT
ENST00000688100.1:n.1553-79_1553-75delinsGGGTT
ENST00000688588.1:c.632-79_632-75delinsGGGTT ENSP00000510802.1:n.632-79_632-75delinsGGGTT
ENST00000688927.1:n.2764_2768delinsGGGTT
ENST00000689283.1:c.*295-79_*295-75delinsGGGTT ENSP00000509050.1:n.*295-79_*295-75delinsGGGTT
ENST00000689477.1:c.*525-79_*525-75delinsGGGTT ENSP00000508945.1:n.*525-79_*525-75delinsGGGTT
ENST00000689765.1:c.*169-123_*169-119delinsGGGTT ENSP00000509625.1:n.*169-123_*169-119delinsGGGTT
ENST00000690512.1:c.*483-79_*483-75delinsGGGTT ENSP00000509793.1:n.*483-79_*483-75delinsGGGTT
ENST00000692039.1:c.*430-79_*430-75delinsGGGTT ENSP00000508821.1:n.*430-79_*430-75delinsGGGTT
ENST00000692336.1:c.656-79_656-75delinsGGGTT ENSP00000508540.1:n.656-79_656-75delinsGGGTT
ENST00000693133.1:n.1033_1037delinsGGGTT
ENST00000263578.10:c.632-79_632-75delinsGGGTT MANE Select ENSP00000263578.5:n.632-79_632-75delinsGGGTT
ENST00000263578.9:c.632-79_632-75delinsGGGTT ENSP00000263578.5:n.632-79_632-75delinsGGGTT
ENST00000524751.5:n.794_798delinsGGGTT
ENST00000525083.5:n.352-79_352-75delinsGGGTT
ENST00000525770.5:c.*264-79_*264-75delinsGGGTT ENSP00000434739.1:n.*264-79_*264-75delinsGGGTT
ENST00000527004.5:c.534-79_534-75delinsGGGTT ENSP00000436374.1:n.534-79_534-75delinsGGGTT
ENST00000530642.1:n.1335_1339delinsGGGTT
ENST00000532101.5:n.855-79_855-75delinsGGGTT
ENST00000532125.1:c.590-79_590-75delinsGGGTT ENSP00000434178.1:n.590-79_590-75delinsGGGTT
ENST00000533395.5:n.365-79_365-75delinsGGGTT
ENST00000533839.5:n.238-546_238-542delinsGGGTT
ENST00000534011.5:n.684-79_684-75delinsGGGTT
ENST00000534315.5:n.944-79_944-75delinsGGGTT
NM_017547.3:c.632-79_632-75delinsGGGTT NP_060017.1:n.632-79_632-75delinsGGGTT
NR_037647.1:n.578-79_578-75delinsGGGTT
NR_037648.1:n.818-79_818-75delinsGGGTT
XM_006718879.2:c.122-79_122-75delinsGGGTT XP_006718942.1:n.122-79_122-75delinsGGGTT
XM_006718880.2:c.-2-79_-2-75delinsGGGTT XP_006718943.1:n.-2-79_-2-75delinsGGGTT
XM_006718881.2:c.-2-79_-2-75delinsGGGTT XP_006718944.1:n.-2-79_-2-75delinsGGGTT
XM_011542895.1:c.122-79_122-75delinsGGGTT XP_011541197.1:n.122-79_122-75delinsGGGTT
XM_011542896.1:c.122-79_122-75delinsGGGTT XP_011541198.1:n.122-79_122-75delinsGGGTT
XM_006718879.3:c.122-79_122-75delinsGGGTT XP_006718942.1:n.122-79_122-75delinsGGGTT
XM_006718881.3:c.-2-79_-2-75delinsGGGTT XP_006718944.1:n.-2-79_-2-75delinsGGGTT
XM_011542895.2:c.122-79_122-75delinsGGGTT XP_011541197.1:n.122-79_122-75delinsGGGTT
XM_011542896.2:c.122-79_122-75delinsGGGTT XP_011541198.1:n.122-79_122-75delinsGGGTT
XM_017018000.2:c.632-79_632-75delinsGGGTT XP_016873489.1:n.632-79_632-75delinsGGGTT
XM_017018001.1:c.122-79_122-75delinsGGGTT XP_016873490.1:n.122-79_122-75delinsGGGTT
XM_017018002.1:c.122-79_122-75delinsGGGTT XP_016873491.1:n.122-79_122-75delinsGGGTT
XM_017018003.2:c.-2-79_-2-75delinsGGGTT XP_016873492.1:n.-2-79_-2-75delinsGGGTT
XM_017018004.1:c.-2-79_-2-75delinsGGGTT XP_016873493.1:n.-2-79_-2-75delinsGGGTT
XM_017018005.1:c.-2-79_-2-75delinsGGGTT XP_016873494.1:n.-2-79_-2-75delinsGGGTT
XM_017018006.2:c.-2-79_-2-75delinsGGGTT XP_016873495.1:n.-2-79_-2-75delinsGGGTT
NM_017547.4:c.632-79_632-75delinsGGGTT MANE Select NP_060017.1:n.632-79_632-75delinsGGGTT
NR_037647.2:n.464-79_464-75delinsGGGTT
NR_037648.2:n.809-79_809-75delinsGGGTT