Canonical Allele Identifier: CA2007079729
Gene: FOXRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126275424G= , CM000673.2:g.126275424G= GRCh38
NC_000011.9:g.126145319G= , CM000673.1:g.126145319G= GRCh37
NC_000011.8:g.125650529G= NCBI36
NG_028029.1:g.11385G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.1212G=
ENST00000532101.6:n.831G=
ENST00000532125.2:c.726G= ENSP00000434178.2:p.Val242=
ENST00000533839.6:c.86-370G= ENSP00000509952.1:n.86-370G=
ENST00000534011.6:n.1021G=
ENST00000685484.1:c.729G= ENSP00000510622.1:p.Val243=
ENST00000685601.1:c.729G= ENSP00000510603.1:p.Val243=
ENST00000685765.1:c.729G= ENSP00000509991.1:p.Val243=
ENST00000685844.1:c.*266G= ENSP00000509820.1:n.*266G=
ENST00000685857.1:n.1468G=
ENST00000686242.1:c.528G= ENSP00000508950.1:n.528G=
ENST00000686888.1:c.*296G= ENSP00000509619.1:n.*296G=
ENST00000687699.1:c.853G= ENSP00000508878.1:n.853G=
ENST00000687786.1:n.2165G=
ENST00000688100.1:n.1650G=
ENST00000688588.1:c.729G= ENSP00000510802.1:p.Val243=
ENST00000688927.1:n.2940G=
ENST00000689283.1:c.*392G= ENSP00000509050.1:n.*392G=
ENST00000689477.1:c.*622G= ENSP00000508945.1:n.*622G=
ENST00000689765.1:c.*222G= ENSP00000509625.1:n.*222G=
ENST00000690512.1:c.*580G= ENSP00000509793.1:n.*580G=
ENST00000692039.1:c.*527G= ENSP00000508821.1:n.*527G=
ENST00000692336.1:c.753G= ENSP00000508540.1:p.Val251=
ENST00000693133.1:n.1209G=
ENST00000263578.10:c.729G= MANE Select ENSP00000263578.5:p.Val243=
ENST00000263578.9:c.729G= ENSP00000263578.5:p.Val243=
ENST00000525083.5:n.449G=
ENST00000525770.5:c.*361G= ENSP00000434739.1:n.*361G=
ENST00000527004.5:c.*73G= ENSP00000436374.1:n.*73G=
ENST00000530642.1:n.1511G=
ENST00000532101.5:n.952G=
ENST00000532125.1:c.687G= ENSP00000434178.1:p.Val229=
ENST00000533395.5:n.462G=
ENST00000533839.5:n.238-370G=
ENST00000534011.5:n.781G=
ENST00000534315.5:n.1041G=
NM_017547.3:c.729G= NP_060017.1:p.Val243=
NR_037647.1:n.675G=
NR_037648.1:n.915G=
XM_006718879.2:c.219G= XP_006718942.1:p.Val73=
XM_006718880.2:c.96G= XP_006718943.1:p.Val32=
XM_006718881.2:c.96G= XP_006718944.1:p.Val32=
XM_011542895.1:c.219G= XP_011541197.1:p.Val73=
XM_011542896.1:c.219G= XP_011541198.1:p.Val73=
XM_006718879.3:c.219G= XP_006718942.1:p.Val73=
XM_006718881.3:c.96G= XP_006718944.1:p.Val32=
XM_011542895.2:c.219G= XP_011541197.1:p.Val73=
XM_011542896.2:c.219G= XP_011541198.1:p.Val73=
XM_017018000.2:c.729G= XP_016873489.1:p.Val243=
XM_017018001.1:c.219G= XP_016873490.1:p.Val73=
XM_017018002.1:c.219G= XP_016873491.1:p.Val73=
XM_017018003.2:c.96G= XP_016873492.1:p.Val32=
XM_017018004.1:c.96G= XP_016873493.1:p.Val32=
XM_017018005.1:c.96G= XP_016873494.1:p.Val32=
XM_017018006.2:c.96G= XP_016873495.1:p.Val32=
NM_017547.4:c.729G= MANE Select NP_060017.1:p.Val243=
NR_037647.2:n.561G=
NR_037648.2:n.906G=