Canonical Allele Identifier: CA2725120185
Gene: FOXRED1 HGNC NCBI

Linked Data

dbSNP Id: rs2135263724

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126275024_126275025insGAGGACGA , CM000673.2:g.126275024_126275025insGAGGACGA GRCh38
NC_000011.9:g.126144919_126144920insGAGGACGA , CM000673.1:g.126144919_126144920insGAGGACGA GRCh37
NC_000011.8:g.125650129_125650130insGAGGACGA NCBI36
NG_028029.1:g.10985_10986insGAGGACGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.812_813insGAGGACGA
ENST00000532101.6:n.734-303_734-302insGAGGACGA
ENST00000532125.2:c.628+3_628+4insGAGGACGA ENSP00000434178.2:n.628+3_628+4insGAGGACGA
ENST00000533839.6:c.86-770_86-769insGAGGACGA ENSP00000509952.1:n.86-770_86-769insGAGGACGA
ENST00000534011.6:n.923+3_923+4insGAGGACGA
ENST00000685484.1:c.631+3_631+4insGAGGACGA ENSP00000510622.1:n.631+3_631+4insGAGGACGA
ENST00000685601.1:c.631+3_631+4insGAGGACGA ENSP00000510603.1:n.631+3_631+4insGAGGACGA
ENST00000685765.1:c.631+3_631+4insGAGGACGA ENSP00000509991.1:n.631+3_631+4insGAGGACGA
ENST00000685844.1:c.*169-303_*169-302insGAGGACGA ENSP00000509820.1:n.*169-303_*169-302insGAGGACGA
ENST00000685857.1:n.1068_1069insGAGGACGA
ENST00000686242.1:c.430+3_430+4insGAGGACGA ENSP00000508950.1:n.430+3_430+4insGAGGACGA
ENST00000686888.1:c.*198+3_*198+4insGAGGACGA ENSP00000509619.1:n.*198+3_*198+4insGAGGACGA
ENST00000687699.1:c.755+3_755+4insGAGGACGA ENSP00000508878.1:n.755+3_755+4insGAGGACGA
ENST00000687786.1:n.2068-303_2068-302insGAGGACGA
ENST00000688100.1:n.1552+3_1552+4insGAGGACGA
ENST00000688588.1:c.631+3_631+4insGAGGACGA ENSP00000510802.1:n.631+3_631+4insGAGGACGA
ENST00000688927.1:n.2540_2541insGAGGACGA
ENST00000689283.1:c.*294+3_*294+4insGAGGACGA ENSP00000509050.1:n.*294+3_*294+4insGAGGACGA
ENST00000689477.1:c.*524+3_*524+4insGAGGACGA ENSP00000508945.1:n.*524+3_*524+4insGAGGACGA
ENST00000689765.1:c.*169-347_*169-346insGAGGACGA ENSP00000509625.1:n.*169-347_*169-346insGAGGACGA
ENST00000690512.1:c.*482+3_*482+4insGAGGACGA ENSP00000509793.1:n.*482+3_*482+4insGAGGACGA
ENST00000692039.1:c.*429+3_*429+4insGAGGACGA ENSP00000508821.1:n.*429+3_*429+4insGAGGACGA
ENST00000692336.1:c.655+3_655+4insGAGGACGA ENSP00000508540.1:n.655+3_655+4insGAGGACGA
ENST00000693133.1:n.809_810insGAGGACGA
ENST00000263578.10:c.631+3_631+4insGAGGACGA MANE Select ENSP00000263578.5:n.631+3_631+4insGAGGACGA
ENST00000263578.9:c.631+3_631+4insGAGGACGA ENSP00000263578.5:n.631+3_631+4insGAGGACGA
ENST00000524751.5:n.570_571insGAGGACGA
ENST00000525083.5:n.352-303_352-302insGAGGACGA
ENST00000525770.5:c.*263+3_*263+4insGAGGACGA ENSP00000434739.1:n.*263+3_*263+4insGAGGACGA
ENST00000527004.5:c.534-303_534-302insGAGGACGA ENSP00000436374.1:n.534-303_534-302insGAGGACGA
ENST00000527875.1:n.464_465insGAGGACGA
ENST00000530642.1:n.1111_1112insGAGGACGA
ENST00000532101.5:n.854+3_854+4insGAGGACGA
ENST00000532125.1:c.589+3_589+4insGAGGACGA ENSP00000434178.1:n.589+3_589+4insGAGGACGA
ENST00000533395.5:n.365-303_365-302insGAGGACGA
ENST00000533839.5:n.238-770_238-769insGAGGACGA
ENST00000534011.5:n.683+3_683+4insGAGGACGA
ENST00000534315.5:n.944-303_944-302insGAGGACGA
NM_017547.3:c.631+3_631+4insGAGGACGA NP_060017.1:n.631+3_631+4insGAGGACGA
NR_037647.1:n.577+3_577+4insGAGGACGA
NR_037648.1:n.817+3_817+4insGAGGACGA
XM_006718879.2:c.121+3_121+4insGAGGACGA XP_006718942.1:n.121+3_121+4insGAGGACGA
XM_006718880.2:c.-2-303_-2-302insGAGGACGA XP_006718943.1:n.-2-303_-2-302insGAGGACGA
XM_006718881.2:c.-2-303_-2-302insGAGGACGA XP_006718944.1:n.-2-303_-2-302insGAGGACGA
XM_011542895.1:c.121+3_121+4insGAGGACGA XP_011541197.1:n.121+3_121+4insGAGGACGA
XM_011542896.1:c.121+3_121+4insGAGGACGA XP_011541198.1:n.121+3_121+4insGAGGACGA
XM_006718879.3:c.121+3_121+4insGAGGACGA XP_006718942.1:n.121+3_121+4insGAGGACGA
XM_006718881.3:c.-2-303_-2-302insGAGGACGA XP_006718944.1:n.-2-303_-2-302insGAGGACGA
XM_011542895.2:c.121+3_121+4insGAGGACGA XP_011541197.1:n.121+3_121+4insGAGGACGA
XM_011542896.2:c.121+3_121+4insGAGGACGA XP_011541198.1:n.121+3_121+4insGAGGACGA
XM_017018000.2:c.631+3_631+4insGAGGACGA XP_016873489.1:n.631+3_631+4insGAGGACGA
XM_017018001.1:c.121+3_121+4insGAGGACGA XP_016873490.1:n.121+3_121+4insGAGGACGA
XM_017018002.1:c.121+3_121+4insGAGGACGA XP_016873491.1:n.121+3_121+4insGAGGACGA
XM_017018003.2:c.-2-303_-2-302insGAGGACGA XP_016873492.1:n.-2-303_-2-302insGAGGACGA
XM_017018004.1:c.-2-303_-2-302insGAGGACGA XP_016873493.1:n.-2-303_-2-302insGAGGACGA
XM_017018005.1:c.-2-303_-2-302insGAGGACGA XP_016873494.1:n.-2-303_-2-302insGAGGACGA
XM_017018006.2:c.-2-303_-2-302insGAGGACGA XP_016873495.1:n.-2-303_-2-302insGAGGACGA
NM_017547.4:c.631+3_631+4insGAGGACGA MANE Select NP_060017.1:n.631+3_631+4insGAGGACGA
NR_037647.2:n.463+3_463+4insGAGGACGA
NR_037648.2:n.808+3_808+4insGAGGACGA