Canonical Allele Identifier: CA383230284

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145321C>G (hg19) ; chr11:g.126275426C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275426C>G , CM000673.2:g.126275426C>G	GRCh38
NC_000011.9:g.126145321C>G , CM000673.1:g.126145321C>G	GRCh37
NC_000011.8:g.125650531C>G	NCBI36
NG_028029.1:g.11387C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1214C>G
ENST00000532101.6:n.833C>G
ENST00000532125.2:c.728C>G	ENSP00000434178.2:p.Thr243Arg
ENST00000533839.6:c.86-368C>G	ENSP00000509952.1:n.86-368C>G
ENST00000534011.6:n.1023C>G
ENST00000685484.1:c.731C>G	ENSP00000510622.1:p.Thr244Arg
ENST00000685601.1:c.731C>G	ENSP00000510603.1:p.Thr244Arg
ENST00000685765.1:c.731C>G	ENSP00000509991.1:p.Thr244Arg
ENST00000685844.1:c.*268C>G	ENSP00000509820.1:n.*268C>G
ENST00000685857.1:n.1470C>G
ENST00000686242.1:c.530C>G	ENSP00000508950.1:n.530C>G
ENST00000686888.1:c.*298C>G	ENSP00000509619.1:n.*298C>G
ENST00000687699.1:c.855C>G	ENSP00000508878.1:n.855C>G
ENST00000687786.1:n.2167C>G
ENST00000688100.1:n.1652C>G
ENST00000688588.1:c.731C>G	ENSP00000510802.1:p.Thr244Arg
ENST00000688927.1:n.2942C>G
ENST00000689283.1:c.*394C>G	ENSP00000509050.1:n.*394C>G
ENST00000689477.1:c.*624C>G	ENSP00000508945.1:n.*624C>G
ENST00000689765.1:c.*224C>G	ENSP00000509625.1:n.*224C>G
ENST00000690512.1:c.*582C>G	ENSP00000509793.1:n.*582C>G
ENST00000692039.1:c.*529C>G	ENSP00000508821.1:n.*529C>G
ENST00000692336.1:c.755C>G	ENSP00000508540.1:p.Thr252Arg
ENST00000693133.1:n.1211C>G
ENST00000263578.10:c.731C>G MANE Select	ENSP00000263578.5:p.Thr244Arg
ENST00000263578.9:c.731C>G	ENSP00000263578.5:p.Thr244Arg
ENST00000525083.5:n.451C>G
ENST00000525770.5:c.*363C>G	ENSP00000434739.1:n.*363C>G
ENST00000527004.5:c.*75C>G	ENSP00000436374.1:n.*75C>G
ENST00000530642.1:n.1513C>G
ENST00000532101.5:n.954C>G
ENST00000532125.1:c.689C>G	ENSP00000434178.1:p.Thr230Arg
ENST00000533395.5:n.464C>G
ENST00000533839.5:n.238-368C>G
ENST00000534011.5:n.783C>G
ENST00000534315.5:n.1043C>G
NM_017547.3:c.731C>G	NP_060017.1:p.Thr244Arg
NR_037647.1:n.677C>G
NR_037648.1:n.917C>G
XM_006718879.2:c.221C>G	XP_006718942.1:p.Thr74Arg
XM_006718880.2:c.98C>G	XP_006718943.1:p.Thr33Arg
XM_006718881.2:c.98C>G	XP_006718944.1:p.Thr33Arg
XM_011542895.1:c.221C>G	XP_011541197.1:p.Thr74Arg
XM_011542896.1:c.221C>G	XP_011541198.1:p.Thr74Arg
XM_006718879.3:c.221C>G	XP_006718942.1:p.Thr74Arg
XM_006718881.3:c.98C>G	XP_006718944.1:p.Thr33Arg
XM_011542895.2:c.221C>G	XP_011541197.1:p.Thr74Arg
XM_011542896.2:c.221C>G	XP_011541198.1:p.Thr74Arg
XM_017018000.2:c.731C>G	XP_016873489.1:p.Thr244Arg
XM_017018001.1:c.221C>G	XP_016873490.1:p.Thr74Arg
XM_017018002.1:c.221C>G	XP_016873491.1:p.Thr74Arg
XM_017018003.2:c.98C>G	XP_016873492.1:p.Thr33Arg
XM_017018004.1:c.98C>G	XP_016873493.1:p.Thr33Arg
XM_017018005.1:c.98C>G	XP_016873494.1:p.Thr33Arg
XM_017018006.2:c.98C>G	XP_016873495.1:p.Thr33Arg
NM_017547.4:c.731C>G MANE Select	NP_060017.1:p.Thr244Arg
NR_037647.2:n.563C>G
NR_037648.2:n.908C>G