Canonical Allele Identifier: CA383229925
Gene: FOXRED1 HGNC NCBI

Linked Data

dbSNP Id: rs750019266

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126274961G>T , CM000673.2:g.126274961G>T GRCh38
NC_000011.9:g.126144856G>T , CM000673.1:g.126144856G>T GRCh37
NC_000011.8:g.125650066G>T NCBI36
NG_028029.1:g.10922G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.749G>T
ENST00000532101.6:n.734-366G>T
ENST00000532125.2:c.568G>T ENSP00000434178.2:p.Asp190Tyr
ENST00000533839.6:c.86-833G>T ENSP00000509952.1:n.86-833G>T
ENST00000534011.6:n.863G>T
ENST00000685484.1:c.571G>T ENSP00000510622.1:p.Asp191Tyr
ENST00000685601.1:c.571G>T ENSP00000510603.1:p.Asp191Tyr
ENST00000685765.1:c.571G>T ENSP00000509991.1:p.Asp191Tyr
ENST00000685844.1:c.*169-366G>T ENSP00000509820.1:n.*169-366G>T
ENST00000685857.1:n.1005G>T
ENST00000686242.1:c.370G>T ENSP00000508950.1:n.370G>T
ENST00000686888.1:c.*138G>T ENSP00000509619.1:n.*138G>T
ENST00000687699.1:c.695G>T ENSP00000508878.1:n.695G>T
ENST00000687786.1:n.2068-366G>T
ENST00000688100.1:n.1492G>T
ENST00000688588.1:c.571G>T ENSP00000510802.1:p.Asp191Tyr
ENST00000688927.1:n.2477G>T
ENST00000689283.1:c.*234G>T ENSP00000509050.1:n.*234G>T
ENST00000689477.1:c.*464G>T ENSP00000508945.1:n.*464G>T
ENST00000689765.1:c.*169-410G>T ENSP00000509625.1:n.*169-410G>T
ENST00000690512.1:c.*422G>T ENSP00000509793.1:n.*422G>T
ENST00000692039.1:c.*369G>T ENSP00000508821.1:n.*369G>T
ENST00000692336.1:c.595G>T ENSP00000508540.1:p.Asp199Tyr
ENST00000693133.1:n.746G>T
ENST00000263578.10:c.571G>T MANE Select ENSP00000263578.5:p.Asp191Tyr
ENST00000263578.9:c.571G>T ENSP00000263578.5:p.Asp191Tyr
ENST00000524751.5:n.507G>T
ENST00000525083.5:n.352-366G>T
ENST00000525770.5:c.*203G>T ENSP00000434739.1:n.*203G>T
ENST00000526366.5:n.502G>T
ENST00000527004.5:c.534-366G>T ENSP00000436374.1:n.534-366G>T
ENST00000527875.1:n.401G>T
ENST00000530642.1:n.1048G>T
ENST00000532101.5:n.794G>T
ENST00000532125.1:c.529G>T ENSP00000434178.1:p.Asp177Tyr
ENST00000533395.5:n.365-366G>T
ENST00000533839.5:n.238-833G>T
ENST00000534011.5:n.623G>T
ENST00000534315.5:n.944-366G>T
NM_017547.3:c.571G>T NP_060017.1:p.Asp191Tyr
NR_037647.1:n.517G>T
NR_037648.1:n.757G>T
XM_006718879.2:c.61G>T XP_006718942.1:p.Asp21Tyr
XM_006718880.2:c.-2-366G>T XP_006718943.1:n.-2-366G>T
XM_006718881.2:c.-2-366G>T XP_006718944.1:n.-2-366G>T
XM_011542895.1:c.61G>T XP_011541197.1:p.Asp21Tyr
XM_011542896.1:c.61G>T XP_011541198.1:p.Asp21Tyr
XM_006718879.3:c.61G>T XP_006718942.1:p.Asp21Tyr
XM_006718881.3:c.-2-366G>T XP_006718944.1:n.-2-366G>T
XM_011542895.2:c.61G>T XP_011541197.1:p.Asp21Tyr
XM_011542896.2:c.61G>T XP_011541198.1:p.Asp21Tyr
XM_017018000.2:c.571G>T XP_016873489.1:p.Asp191Tyr
XM_017018001.1:c.61G>T XP_016873490.1:p.Asp21Tyr
XM_017018002.1:c.61G>T XP_016873491.1:p.Asp21Tyr
XM_017018003.2:c.-2-366G>T XP_016873492.1:n.-2-366G>T
XM_017018004.1:c.-2-366G>T XP_016873493.1:n.-2-366G>T
XM_017018005.1:c.-2-366G>T XP_016873494.1:n.-2-366G>T
XM_017018006.2:c.-2-366G>T XP_016873495.1:n.-2-366G>T
NM_017547.4:c.571G>T MANE Select NP_060017.1:p.Asp191Tyr
NR_037647.2:n.403G>T
NR_037648.2:n.748G>T