Canonical Allele Identifier: CA323382

Gene: FOXRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126269213C>T , CM000673.2:g.126269213C>T	GRCh38
NC_000011.9:g.126139108C>T , CM000673.1:g.126139108C>T	GRCh37
NC_000011.8:g.125644318C>T	NCBI36
NG_028029.1:g.5174C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.185C>T
ENST00000532125.2:c.7C>T	ENSP00000434178.2:p.Arg3Trp
ENST00000533839.6:c.7C>T	ENSP00000509952.1:p.Arg3Trp
ENST00000534011.6:n.66C>T
ENST00000685484.1:c.7C>T	ENSP00000510622.1:p.Arg3Trp
ENST00000685601.1:c.7C>T	ENSP00000510603.1:p.Arg3Trp
ENST00000685765.1:c.7C>T	ENSP00000509991.1:p.Arg3Trp
ENST00000685844.1:c.7C>T	ENSP00000509820.1:p.Arg3Trp
ENST00000685857.1:n.185C>T
ENST00000686242.1:c.7C>T	ENSP00000508950.1:p.Arg3Trp
ENST00000686888.1:c.7C>T	ENSP00000509619.1:p.Arg3Trp
ENST00000687699.1:c.7C>T	ENSP00000508878.1:p.Arg3Trp
ENST00000688588.1:c.7C>T	ENSP00000510802.1:p.Arg3Trp
ENST00000688927.1:n.185C>T
ENST00000689283.1:c.7C>T	ENSP00000509050.1:p.Arg3Trp
ENST00000689477.1:c.7C>T	ENSP00000508945.1:p.Arg3Trp
ENST00000689765.1:c.7C>T	ENSP00000509625.1:p.Arg3Trp
ENST00000690512.1:c.7C>T	ENSP00000509793.1:p.Arg3Trp
ENST00000692039.1:c.7C>T	ENSP00000508821.1:p.Arg3Trp
ENST00000692336.1:c.7C>T	ENSP00000508540.1:p.Arg3Trp
ENST00000693133.1:n.23C>T
ENST00000263578.10:c.7C>T MANE Select	ENSP00000263578.5:p.Arg3Trp
ENST00000263578.9:c.7C>T	ENSP00000263578.5:p.Arg3Trp
ENST00000524751.5:n.20C>T
ENST00000525083.5:n.43C>T
ENST00000525770.5:c.7C>T	ENSP00000434739.1:p.Arg3Trp
ENST00000526366.5:n.22C>T
ENST00000526525.1:n.43C>T
ENST00000527004.5:c.7C>T	ENSP00000436374.1:p.Arg3Trp
ENST00000529802.1:n.57C>T
ENST00000532101.5:n.13C>T
ENST00000532125.1:c.-160C>T	ENSP00000434178.1:n.-160C>T
ENST00000533839.5:n.159C>T
ENST00000534011.5:n.79C>T
NM_017547.3:c.7C>T	NP_060017.1:p.Arg3Trp
NR_037647.1:n.174C>T
NR_037648.1:n.69C>T
XM_006718881.2:c.-311C>T	XP_006718944.1:n.-311C>T
XM_011542895.1:c.-721C>T	XP_011541197.1:n.-721C>T
XM_011542896.1:c.-524C>T	XP_011541198.1:n.-524C>T
XM_006718881.3:c.-311C>T	XP_006718944.1:n.-311C>T
XM_011542895.2:c.-721C>T	XP_011541197.1:n.-721C>T
XM_011542896.2:c.-524C>T	XP_011541198.1:n.-524C>T
XM_017018000.2:c.7C>T	XP_016873489.1:p.Arg3Trp
XM_017018001.1:c.-648C>T	XP_016873490.1:n.-648C>T
XM_017018002.1:c.-303C>T	XP_016873491.1:n.-303C>T
XM_017018003.2:c.-532C>T	XP_016873492.1:n.-532C>T
XM_017018004.1:c.-749C>T	XP_016873493.1:n.-749C>T
XM_017018006.2:c.-532C>T	XP_016873495.1:n.-532C>T
NM_017547.4:c.7C>T MANE Select	NP_060017.1:p.Arg3Trp
NR_037647.2:n.60C>T
NR_037648.2:n.60C>T