Canonical Allele Identifier: CA325035

Gene: FOXRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126269231G>C , CM000673.2:g.126269231G>C	GRCh38
NC_000011.9:g.126139126G>C , CM000673.1:g.126139126G>C	GRCh37
NC_000011.8:g.125644336G>C	NCBI36
NG_028029.1:g.5192G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.203G>C
ENST00000532125.2:c.25G>C	ENSP00000434178.2:p.Gly9Arg
ENST00000533839.6:c.25G>C	ENSP00000509952.1:p.Gly9Arg
ENST00000534011.6:n.84G>C
ENST00000685484.1:c.25G>C	ENSP00000510622.1:p.Gly9Arg
ENST00000685601.1:c.25G>C	ENSP00000510603.1:p.Gly9Arg
ENST00000685765.1:c.25G>C	ENSP00000509991.1:p.Gly9Arg
ENST00000685844.1:c.25G>C	ENSP00000509820.1:p.Gly9Arg
ENST00000685857.1:n.203G>C
ENST00000686242.1:c.25G>C	ENSP00000508950.1:p.Gly9Arg
ENST00000686888.1:c.25G>C	ENSP00000509619.1:p.Gly9Arg
ENST00000687699.1:c.25G>C	ENSP00000508878.1:p.Gly9Arg
ENST00000688588.1:c.25G>C	ENSP00000510802.1:p.Gly9Arg
ENST00000688927.1:n.203G>C
ENST00000689283.1:c.25G>C	ENSP00000509050.1:p.Gly9Arg
ENST00000689477.1:c.25G>C	ENSP00000508945.1:p.Gly9Arg
ENST00000689765.1:c.25G>C	ENSP00000509625.1:p.Gly9Arg
ENST00000690512.1:c.25G>C	ENSP00000509793.1:p.Gly9Arg
ENST00000692039.1:c.25G>C	ENSP00000508821.1:p.Gly9Arg
ENST00000692336.1:c.25G>C	ENSP00000508540.1:p.Gly9Arg
ENST00000693133.1:n.41G>C
ENST00000263578.10:c.25G>C MANE Select	ENSP00000263578.5:p.Gly9Arg
ENST00000263578.9:c.25G>C	ENSP00000263578.5:p.Gly9Arg
ENST00000524751.5:n.38G>C
ENST00000525083.5:n.61G>C
ENST00000525770.5:c.25G>C	ENSP00000434739.1:p.Gly9Arg
ENST00000526366.5:n.40G>C
ENST00000526525.1:n.61G>C
ENST00000527004.5:c.25G>C	ENSP00000436374.1:p.Gly9Arg
ENST00000529802.1:n.75G>C
ENST00000532101.5:n.31G>C
ENST00000532125.1:c.-142G>C	ENSP00000434178.1:n.-142G>C
ENST00000533839.5:n.177G>C
ENST00000534011.5:n.97G>C
NM_017547.3:c.25G>C	NP_060017.1:p.Gly9Arg
NR_037647.1:n.192G>C
NR_037648.1:n.87G>C
XM_006718881.2:c.-293G>C	XP_006718944.1:n.-293G>C
XM_011542895.1:c.-703G>C	XP_011541197.1:n.-703G>C
XM_011542896.1:c.-506G>C	XP_011541198.1:n.-506G>C
XM_006718881.3:c.-293G>C	XP_006718944.1:n.-293G>C
XM_011542895.2:c.-703G>C	XP_011541197.1:n.-703G>C
XM_011542896.2:c.-506G>C	XP_011541198.1:n.-506G>C
XM_017018000.2:c.25G>C	XP_016873489.1:p.Gly9Arg
XM_017018001.1:c.-630G>C	XP_016873490.1:n.-630G>C
XM_017018002.1:c.-285G>C	XP_016873491.1:n.-285G>C
XM_017018003.2:c.-514G>C	XP_016873492.1:n.-514G>C
XM_017018004.1:c.-731G>C	XP_016873493.1:n.-731G>C
XM_017018006.2:c.-514G>C	XP_016873495.1:n.-514G>C
NM_017547.4:c.25G>C MANE Select	NP_060017.1:p.Gly9Arg
NR_037647.2:n.78G>C
NR_037648.2:n.78G>C