Canonical Allele Identifier: CA2007079698
Gene: FOXRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126275346G= , CM000673.2:g.126275346G= GRCh38
NC_000011.9:g.126145241G= , CM000673.1:g.126145241G= GRCh37
NC_000011.8:g.125650451G= NCBI36
NG_028029.1:g.11307G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.1134G=
ENST00000532101.6:n.753G=
ENST00000532125.2:c.648G= ENSP00000434178.2:p.Trp216=
ENST00000533839.6:c.86-448G= ENSP00000509952.1:n.86-448G=
ENST00000534011.6:n.943G=
ENST00000685484.1:c.651G= ENSP00000510622.1:p.Trp217=
ENST00000685601.1:c.651G= ENSP00000510603.1:p.Trp217=
ENST00000685765.1:c.651G= ENSP00000509991.1:p.Trp217=
ENST00000685844.1:c.*188G= ENSP00000509820.1:n.*188G=
ENST00000685857.1:n.1390G=
ENST00000686242.1:c.450G= ENSP00000508950.1:n.450G=
ENST00000686888.1:c.*218G= ENSP00000509619.1:n.*218G=
ENST00000687699.1:c.775G= ENSP00000508878.1:n.775G=
ENST00000687786.1:n.2087G=
ENST00000688100.1:n.1572G=
ENST00000688588.1:c.651G= ENSP00000510802.1:p.Trp217=
ENST00000688927.1:n.2862G=
ENST00000689283.1:c.*314G= ENSP00000509050.1:n.*314G=
ENST00000689477.1:c.*544G= ENSP00000508945.1:n.*544G=
ENST00000689765.1:c.*169-25G= ENSP00000509625.1:n.*169-25G=
ENST00000690512.1:c.*502G= ENSP00000509793.1:n.*502G=
ENST00000692039.1:c.*449G= ENSP00000508821.1:n.*449G=
ENST00000692336.1:c.675G= ENSP00000508540.1:p.Trp225=
ENST00000693133.1:n.1131G=
ENST00000263578.10:c.651G= MANE Select ENSP00000263578.5:p.Trp217=
ENST00000263578.9:c.651G= ENSP00000263578.5:p.Trp217=
ENST00000524751.5:n.892G=
ENST00000525083.5:n.371G=
ENST00000525770.5:c.*283G= ENSP00000434739.1:n.*283G=
ENST00000527004.5:c.553G= ENSP00000436374.1:p.Val185=
ENST00000530642.1:n.1433G=
ENST00000532101.5:n.874G=
ENST00000532125.1:c.609G= ENSP00000434178.1:p.Trp203=
ENST00000533395.5:n.384G=
ENST00000533839.5:n.238-448G=
ENST00000534011.5:n.703G=
ENST00000534315.5:n.963G=
NM_017547.3:c.651G= NP_060017.1:p.Trp217=
NR_037647.1:n.597G=
NR_037648.1:n.837G=
XM_006718879.2:c.141G= XP_006718942.1:p.Trp47=
XM_006718880.2:c.18G= XP_006718943.1:p.Trp6=
XM_006718881.2:c.18G= XP_006718944.1:p.Trp6=
XM_011542895.1:c.141G= XP_011541197.1:p.Trp47=
XM_011542896.1:c.141G= XP_011541198.1:p.Trp47=
XM_006718879.3:c.141G= XP_006718942.1:p.Trp47=
XM_006718881.3:c.18G= XP_006718944.1:p.Trp6=
XM_011542895.2:c.141G= XP_011541197.1:p.Trp47=
XM_011542896.2:c.141G= XP_011541198.1:p.Trp47=
XM_017018000.2:c.651G= XP_016873489.1:p.Trp217=
XM_017018001.1:c.141G= XP_016873490.1:p.Trp47=
XM_017018002.1:c.141G= XP_016873491.1:p.Trp47=
XM_017018003.2:c.18G= XP_016873492.1:p.Trp6=
XM_017018004.1:c.18G= XP_016873493.1:p.Trp6=
XM_017018005.1:c.18G= XP_016873494.1:p.Trp6=
XM_017018006.2:c.18G= XP_016873495.1:p.Trp6=
NM_017547.4:c.651G= MANE Select NP_060017.1:p.Trp217=
NR_037647.2:n.483G=
NR_037648.2:n.828G=