Canonical Allele Identifier: CA477516085

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145277A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275382A>C , CM000673.2:g.126275382A>C	GRCh38
NC_000011.9:g.126145277A>C , CM000673.1:g.126145277A>C	GRCh37
NC_000011.8:g.125650487A>C	NCBI36
NG_028029.1:g.11343A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1170A>C
ENST00000532101.6:n.789A>C
ENST00000532125.2:c.684A>C	ENSP00000434178.2:p.Arg228=
ENST00000533839.6:c.86-412A>C	ENSP00000509952.1:n.86-412A>C
ENST00000534011.6:n.979A>C
ENST00000685484.1:c.687A>C	ENSP00000510622.1:p.Arg229=
ENST00000685601.1:c.687A>C	ENSP00000510603.1:p.Arg229=
ENST00000685765.1:c.687A>C	ENSP00000509991.1:p.Arg229=
ENST00000685844.1:c.*224A>C	ENSP00000509820.1:n.*224A>C
ENST00000685857.1:n.1426A>C
ENST00000686242.1:c.486A>C	ENSP00000508950.1:n.486A>C
ENST00000686888.1:c.*254A>C	ENSP00000509619.1:n.*254A>C
ENST00000687699.1:c.811A>C	ENSP00000508878.1:n.811A>C
ENST00000687786.1:n.2123A>C
ENST00000688100.1:n.1608A>C
ENST00000688588.1:c.687A>C	ENSP00000510802.1:p.Arg229=
ENST00000688927.1:n.2898A>C
ENST00000689283.1:c.*350A>C	ENSP00000509050.1:n.*350A>C
ENST00000689477.1:c.*580A>C	ENSP00000508945.1:n.*580A>C
ENST00000689765.1:c.*180A>C	ENSP00000509625.1:n.*180A>C
ENST00000690512.1:c.*538A>C	ENSP00000509793.1:n.*538A>C
ENST00000692039.1:c.*485A>C	ENSP00000508821.1:n.*485A>C
ENST00000692336.1:c.711A>C	ENSP00000508540.1:p.Arg237=
ENST00000693133.1:n.1167A>C
ENST00000263578.10:c.687A>C MANE Select	ENSP00000263578.5:p.Arg229=
ENST00000263578.9:c.687A>C	ENSP00000263578.5:p.Arg229=
ENST00000525083.5:n.407A>C
ENST00000525770.5:c.*319A>C	ENSP00000434739.1:n.*319A>C
ENST00000527004.5:c.*31A>C	ENSP00000436374.1:n.*31A>C
ENST00000530642.1:n.1469A>C
ENST00000532101.5:n.910A>C
ENST00000532125.1:c.645A>C	ENSP00000434178.1:p.Arg215=
ENST00000533395.5:n.420A>C
ENST00000533839.5:n.238-412A>C
ENST00000534011.5:n.739A>C
ENST00000534315.5:n.999A>C
NM_017547.3:c.687A>C	NP_060017.1:p.Arg229=
NR_037647.1:n.633A>C
NR_037648.1:n.873A>C
XM_006718879.2:c.177A>C	XP_006718942.1:p.Arg59=
XM_006718880.2:c.54A>C	XP_006718943.1:p.Arg18=
XM_006718881.2:c.54A>C	XP_006718944.1:p.Arg18=
XM_011542895.1:c.177A>C	XP_011541197.1:p.Arg59=
XM_011542896.1:c.177A>C	XP_011541198.1:p.Arg59=
XM_006718879.3:c.177A>C	XP_006718942.1:p.Arg59=
XM_006718881.3:c.54A>C	XP_006718944.1:p.Arg18=
XM_011542895.2:c.177A>C	XP_011541197.1:p.Arg59=
XM_011542896.2:c.177A>C	XP_011541198.1:p.Arg59=
XM_017018000.2:c.687A>C	XP_016873489.1:p.Arg229=
XM_017018001.1:c.177A>C	XP_016873490.1:p.Arg59=
XM_017018002.1:c.177A>C	XP_016873491.1:p.Arg59=
XM_017018003.2:c.54A>C	XP_016873492.1:p.Arg18=
XM_017018004.1:c.54A>C	XP_016873493.1:p.Arg18=
XM_017018005.1:c.54A>C	XP_016873494.1:p.Arg18=
XM_017018006.2:c.54A>C	XP_016873495.1:p.Arg18=
NM_017547.4:c.687A>C MANE Select	NP_060017.1:p.Arg229=
NR_037647.2:n.519A>C
NR_037648.2:n.864A>C