Canonical Allele Identifier: CA2007079744
Gene: FOXRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126275462G= , CM000673.2:g.126275462G= GRCh38
NC_000011.9:g.126145357G= , CM000673.1:g.126145357G= GRCh37
NC_000011.8:g.125650567G= NCBI36
NG_028029.1:g.11423G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.1216+34G=
ENST00000532101.6:n.835+34G=
ENST00000532125.2:c.730+34G= ENSP00000434178.2:n.730+34G=
ENST00000533839.6:c.86-332G= ENSP00000509952.1:n.86-332G=
ENST00000534011.6:n.1025+34G=
ENST00000685484.1:c.733+34G= ENSP00000510622.1:n.733+34G=
ENST00000685601.1:c.733+34G= ENSP00000510603.1:n.733+34G=
ENST00000685765.1:c.733+34G= ENSP00000509991.1:n.733+34G=
ENST00000685844.1:c.*270+34G= ENSP00000509820.1:n.*270+34G=
ENST00000685857.1:n.1506G=
ENST00000686242.1:c.532+34G= ENSP00000508950.1:n.532+34G=
ENST00000686888.1:c.*300+34G= ENSP00000509619.1:n.*300+34G=
ENST00000687699.1:c.857+34G= ENSP00000508878.1:n.857+34G=
ENST00000687786.1:n.2169+34G=
ENST00000688100.1:n.1654+34G=
ENST00000688588.1:c.733+34G= ENSP00000510802.1:n.733+34G=
ENST00000688927.1:n.2944+34G=
ENST00000689283.1:c.*396+34G= ENSP00000509050.1:n.*396+34G=
ENST00000689477.1:c.*626+34G= ENSP00000508945.1:n.*626+34G=
ENST00000689765.1:c.*226+34G= ENSP00000509625.1:n.*226+34G=
ENST00000690512.1:c.*584+34G= ENSP00000509793.1:n.*584+34G=
ENST00000692039.1:c.*531+34G= ENSP00000508821.1:n.*531+34G=
ENST00000692336.1:c.757+34G= ENSP00000508540.1:n.757+34G=
ENST00000693133.1:n.1247G=
ENST00000263578.10:c.733+34G= MANE Select ENSP00000263578.5:n.733+34G=
ENST00000263578.9:c.733+34G= ENSP00000263578.5:n.733+34G=
ENST00000525083.5:n.453+34G=
ENST00000525770.5:c.*365+34G= ENSP00000434739.1:n.*365+34G=
ENST00000527004.5:c.*77+34G= ENSP00000436374.1:n.*77+34G=
ENST00000530642.1:n.1549G=
ENST00000532101.5:n.956+34G=
ENST00000532125.1:c.691+34G= ENSP00000434178.1:n.691+34G=
ENST00000533395.5:n.466+34G=
ENST00000533839.5:n.238-332G=
ENST00000534011.5:n.785+34G=
ENST00000534315.5:n.1045+34G=
NM_017547.3:c.733+34G= NP_060017.1:n.733+34G=
NR_037647.1:n.679+34G=
NR_037648.1:n.919+34G=
XM_006718879.2:c.223+34G= XP_006718942.1:n.223+34G=
XM_006718880.2:c.100+34G= XP_006718943.1:n.100+34G=
XM_006718881.2:c.100+34G= XP_006718944.1:n.100+34G=
XM_011542895.1:c.223+34G= XP_011541197.1:n.223+34G=
XM_011542896.1:c.223+34G= XP_011541198.1:n.223+34G=
XM_006718879.3:c.223+34G= XP_006718942.1:n.223+34G=
XM_006718881.3:c.100+34G= XP_006718944.1:n.100+34G=
XM_011542895.2:c.223+34G= XP_011541197.1:n.223+34G=
XM_011542896.2:c.223+34G= XP_011541198.1:n.223+34G=
XM_017018000.2:c.733+34G= XP_016873489.1:n.733+34G=
XM_017018001.1:c.223+34G= XP_016873490.1:n.223+34G=
XM_017018002.1:c.223+34G= XP_016873491.1:n.223+34G=
XM_017018003.2:c.100+34G= XP_016873492.1:n.100+34G=
XM_017018004.1:c.100+34G= XP_016873493.1:n.100+34G=
XM_017018005.1:c.100+34G= XP_016873494.1:n.100+34G=
XM_017018006.2:c.100+34G= XP_016873495.1:n.100+34G=
NM_017547.4:c.733+34G= MANE Select NP_060017.1:n.733+34G=
NR_037647.2:n.565+34G=
NR_037648.2:n.910+34G=