Canonical Allele Identifier: CA2007076477
Gene: FOXRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126271136C= , CM000673.2:g.126271136C= GRCh38
NC_000011.9:g.126141031C= , CM000673.1:g.126141031C= GRCh37
NC_000011.8:g.125646241C= NCBI36
NG_028029.1:g.7097C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.264-301C=
ENST00000532101.6:n.46-84C=
ENST00000532125.2:c.86-301C= ENSP00000434178.2:n.86-301C=
ENST00000533839.6:c.85+1845C= ENSP00000509952.1:n.85+1845C=
ENST00000534011.6:n.145-84C=
ENST00000685484.1:c.86-301C= ENSP00000510622.1:n.86-301C=
ENST00000685601.1:c.86-301C= ENSP00000510603.1:n.86-301C=
ENST00000685765.1:c.86-301C= ENSP00000509991.1:n.86-301C=
ENST00000685844.1:c.86-1833C= ENSP00000509820.1:n.86-1833C=
ENST00000685857.1:n.264-301C=
ENST00000686242.1:c.86-1833C= ENSP00000508950.1:n.86-1833C=
ENST00000686888.1:c.86-301C= ENSP00000509619.1:n.86-301C=
ENST00000687699.1:c.210-301C= ENSP00000508878.1:n.210-301C=
ENST00000687786.1:n.1118C=
ENST00000688588.1:c.86-301C= ENSP00000510802.1:n.86-301C=
ENST00000688927.1:n.264-301C=
ENST00000689283.1:c.209+1721C= ENSP00000509050.1:n.209+1721C=
ENST00000689477.1:c.86-84C= ENSP00000508945.1:n.86-84C=
ENST00000689765.1:c.86-1833C= ENSP00000509625.1:n.86-1833C=
ENST00000690512.1:c.86-1342C= ENSP00000509793.1:n.86-1342C=
ENST00000692039.1:c.86-215C= ENSP00000508821.1:n.86-215C=
ENST00000692336.1:c.86-301C= ENSP00000508540.1:n.86-301C=
ENST00000693133.1:n.225+1721C=
ENST00000263578.10:c.86-301C= MANE Select ENSP00000263578.5:n.86-301C=
ENST00000263578.9:c.86-301C= ENSP00000263578.5:n.86-301C=
ENST00000524751.5:n.222+1721C=
ENST00000525083.5:n.122-1833C=
ENST00000525770.5:c.86-1833C= ENSP00000434739.1:n.86-1833C=
ENST00000526366.5:n.101-583C=
ENST00000526525.1:n.245+1721C=
ENST00000527004.5:c.86-301C= ENSP00000436374.1:n.86-301C=
ENST00000529802.1:n.136-301C=
ENST00000532101.5:n.92-84C=
ENST00000532125.1:c.44-301C= ENSP00000434178.1:n.44-301C=
ENST00000533839.5:n.237+1845C=
ENST00000534011.5:n.158-1342C=
ENST00000534315.5:n.192C=
NM_017547.3:c.86-301C= NP_060017.1:n.86-301C=
NR_037647.1:n.253-1833C=
NR_037648.1:n.272-301C=
XM_006718880.2:c.-754C= XP_006718943.1:n.-754C=
XM_006718881.2:c.-232-1833C= XP_006718944.1:n.-232-1833C=
XM_011542895.1:c.-642-84C= XP_011541197.1:n.-642-84C=
XM_011542896.1:c.-445-301C= XP_011541198.1:n.-445-301C=
XM_006718881.3:c.-232-1833C= XP_006718944.1:n.-232-1833C=
XM_011542895.2:c.-642-84C= XP_011541197.1:n.-642-84C=
XM_011542896.2:c.-445-301C= XP_011541198.1:n.-445-301C=
XM_017018000.2:c.86-301C= XP_016873489.1:n.86-301C=
XM_017018001.1:c.-445-301C= XP_016873490.1:n.-445-301C=
XM_017018002.1:c.-224-1833C= XP_016873491.1:n.-224-1833C=
XM_017018003.2:c.-453-301C= XP_016873492.1:n.-453-301C=
XM_017018004.1:c.-670-84C= XP_016873493.1:n.-670-84C=
XM_017018005.1:c.-952C= XP_016873494.1:n.-952C=
XM_017018006.2:c.-453-301C= XP_016873495.1:n.-453-301C=
NM_017547.4:c.86-301C= MANE Select NP_060017.1:n.86-301C=
NR_037647.2:n.139-1833C=
NR_037648.2:n.263-301C=