Canonical Allele Identifier: CA383230261

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145311G>C (hg19) ; chr11:g.126275416G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275416G>C , CM000673.2:g.126275416G>C	GRCh38
NC_000011.9:g.126145311G>C , CM000673.1:g.126145311G>C	GRCh37
NC_000011.8:g.125650521G>C	NCBI36
NG_028029.1:g.11377G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1204G>C
ENST00000532101.6:n.823G>C
ENST00000532125.2:c.718G>C	ENSP00000434178.2:p.Gly240Arg
ENST00000533839.6:c.86-378G>C	ENSP00000509952.1:n.86-378G>C
ENST00000534011.6:n.1013G>C
ENST00000685484.1:c.721G>C	ENSP00000510622.1:p.Gly241Arg
ENST00000685601.1:c.721G>C	ENSP00000510603.1:p.Gly241Arg
ENST00000685765.1:c.721G>C	ENSP00000509991.1:p.Gly241Arg
ENST00000685844.1:c.*258G>C	ENSP00000509820.1:n.*258G>C
ENST00000685857.1:n.1460G>C
ENST00000686242.1:c.520G>C	ENSP00000508950.1:n.520G>C
ENST00000686888.1:c.*288G>C	ENSP00000509619.1:n.*288G>C
ENST00000687699.1:c.845G>C	ENSP00000508878.1:n.845G>C
ENST00000687786.1:n.2157G>C
ENST00000688100.1:n.1642G>C
ENST00000688588.1:c.721G>C	ENSP00000510802.1:p.Gly241Arg
ENST00000688927.1:n.2932G>C
ENST00000689283.1:c.*384G>C	ENSP00000509050.1:n.*384G>C
ENST00000689477.1:c.*614G>C	ENSP00000508945.1:n.*614G>C
ENST00000689765.1:c.*214G>C	ENSP00000509625.1:n.*214G>C
ENST00000690512.1:c.*572G>C	ENSP00000509793.1:n.*572G>C
ENST00000692039.1:c.*519G>C	ENSP00000508821.1:n.*519G>C
ENST00000692336.1:c.745G>C	ENSP00000508540.1:p.Gly249Arg
ENST00000693133.1:n.1201G>C
ENST00000263578.10:c.721G>C MANE Select	ENSP00000263578.5:p.Gly241Arg
ENST00000263578.9:c.721G>C	ENSP00000263578.5:p.Gly241Arg
ENST00000525083.5:n.441G>C
ENST00000525770.5:c.*353G>C	ENSP00000434739.1:n.*353G>C
ENST00000527004.5:c.*65G>C	ENSP00000436374.1:n.*65G>C
ENST00000530642.1:n.1503G>C
ENST00000532101.5:n.944G>C
ENST00000532125.1:c.679G>C	ENSP00000434178.1:p.Gly227Arg
ENST00000533395.5:n.454G>C
ENST00000533839.5:n.238-378G>C
ENST00000534011.5:n.773G>C
ENST00000534315.5:n.1033G>C
NM_017547.3:c.721G>C	NP_060017.1:p.Gly241Arg
NR_037647.1:n.667G>C
NR_037648.1:n.907G>C
XM_006718879.2:c.211G>C	XP_006718942.1:p.Gly71Arg
XM_006718880.2:c.88G>C	XP_006718943.1:p.Gly30Arg
XM_006718881.2:c.88G>C	XP_006718944.1:p.Gly30Arg
XM_011542895.1:c.211G>C	XP_011541197.1:p.Gly71Arg
XM_011542896.1:c.211G>C	XP_011541198.1:p.Gly71Arg
XM_006718879.3:c.211G>C	XP_006718942.1:p.Gly71Arg
XM_006718881.3:c.88G>C	XP_006718944.1:p.Gly30Arg
XM_011542895.2:c.211G>C	XP_011541197.1:p.Gly71Arg
XM_011542896.2:c.211G>C	XP_011541198.1:p.Gly71Arg
XM_017018000.2:c.721G>C	XP_016873489.1:p.Gly241Arg
XM_017018001.1:c.211G>C	XP_016873490.1:p.Gly71Arg
XM_017018002.1:c.211G>C	XP_016873491.1:p.Gly71Arg
XM_017018003.2:c.88G>C	XP_016873492.1:p.Gly30Arg
XM_017018004.1:c.88G>C	XP_016873493.1:p.Gly30Arg
XM_017018005.1:c.88G>C	XP_016873494.1:p.Gly30Arg
XM_017018006.2:c.88G>C	XP_016873495.1:p.Gly30Arg
NM_017547.4:c.721G>C MANE Select	NP_060017.1:p.Gly241Arg
NR_037647.2:n.553G>C
NR_037648.2:n.898G>C