Canonical Allele Identifier: CA477515233

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126144867G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274972G>C , CM000673.2:g.126274972G>C	GRCh38
NC_000011.9:g.126144867G>C , CM000673.1:g.126144867G>C	GRCh37
NC_000011.8:g.125650077G>C	NCBI36
NG_028029.1:g.10933G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.760G>C
ENST00000532101.6:n.734-355G>C
ENST00000532125.2:c.579G>C	ENSP00000434178.2:p.Arg193=
ENST00000533839.6:c.86-822G>C	ENSP00000509952.1:n.86-822G>C
ENST00000534011.6:n.874G>C
ENST00000685484.1:c.582G>C	ENSP00000510622.1:p.Arg194=
ENST00000685601.1:c.582G>C	ENSP00000510603.1:p.Arg194=
ENST00000685765.1:c.582G>C	ENSP00000509991.1:p.Arg194=
ENST00000685844.1:c.*169-355G>C	ENSP00000509820.1:n.*169-355G>C
ENST00000685857.1:n.1016G>C
ENST00000686242.1:c.381G>C	ENSP00000508950.1:n.381G>C
ENST00000686888.1:c.*149G>C	ENSP00000509619.1:n.*149G>C
ENST00000687699.1:c.706G>C	ENSP00000508878.1:n.706G>C
ENST00000687786.1:n.2068-355G>C
ENST00000688100.1:n.1503G>C
ENST00000688588.1:c.582G>C	ENSP00000510802.1:p.Arg194=
ENST00000688927.1:n.2488G>C
ENST00000689283.1:c.*245G>C	ENSP00000509050.1:n.*245G>C
ENST00000689477.1:c.*475G>C	ENSP00000508945.1:n.*475G>C
ENST00000689765.1:c.*169-399G>C	ENSP00000509625.1:n.*169-399G>C
ENST00000690512.1:c.*433G>C	ENSP00000509793.1:n.*433G>C
ENST00000692039.1:c.*380G>C	ENSP00000508821.1:n.*380G>C
ENST00000692336.1:c.606G>C	ENSP00000508540.1:p.Arg202=
ENST00000693133.1:n.757G>C
ENST00000263578.10:c.582G>C MANE Select	ENSP00000263578.5:p.Arg194=
ENST00000263578.9:c.582G>C	ENSP00000263578.5:p.Arg194=
ENST00000524751.5:n.518G>C
ENST00000525083.5:n.352-355G>C
ENST00000525770.5:c.*214G>C	ENSP00000434739.1:n.*214G>C
ENST00000526366.5:n.513G>C
ENST00000527004.5:c.534-355G>C	ENSP00000436374.1:n.534-355G>C
ENST00000527875.1:n.412G>C
ENST00000530642.1:n.1059G>C
ENST00000532101.5:n.805G>C
ENST00000532125.1:c.540G>C	ENSP00000434178.1:p.Arg180=
ENST00000533395.5:n.365-355G>C
ENST00000533839.5:n.238-822G>C
ENST00000534011.5:n.634G>C
ENST00000534315.5:n.944-355G>C
NM_017547.3:c.582G>C	NP_060017.1:p.Arg194=
NR_037647.1:n.528G>C
NR_037648.1:n.768G>C
XM_006718879.2:c.72G>C	XP_006718942.1:p.Arg24=
XM_006718880.2:c.-2-355G>C	XP_006718943.1:n.-2-355G>C
XM_006718881.2:c.-2-355G>C	XP_006718944.1:n.-2-355G>C
XM_011542895.1:c.72G>C	XP_011541197.1:p.Arg24=
XM_011542896.1:c.72G>C	XP_011541198.1:p.Arg24=
XM_006718879.3:c.72G>C	XP_006718942.1:p.Arg24=
XM_006718881.3:c.-2-355G>C	XP_006718944.1:n.-2-355G>C
XM_011542895.2:c.72G>C	XP_011541197.1:p.Arg24=
XM_011542896.2:c.72G>C	XP_011541198.1:p.Arg24=
XM_017018000.2:c.582G>C	XP_016873489.1:p.Arg194=
XM_017018001.1:c.72G>C	XP_016873490.1:p.Arg24=
XM_017018002.1:c.72G>C	XP_016873491.1:p.Arg24=
XM_017018003.2:c.-2-355G>C	XP_016873492.1:n.-2-355G>C
XM_017018004.1:c.-2-355G>C	XP_016873493.1:n.-2-355G>C
XM_017018005.1:c.-2-355G>C	XP_016873494.1:n.-2-355G>C
XM_017018006.2:c.-2-355G>C	XP_016873495.1:n.-2-355G>C
NM_017547.4:c.582G>C MANE Select	NP_060017.1:p.Arg194=
NR_037647.2:n.414G>C
NR_037648.2:n.759G>C