Canonical Allele Identifier: CA383230203

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145285A>G (hg19) ; chr11:g.126275390A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275390A>G , CM000673.2:g.126275390A>G	GRCh38
NC_000011.9:g.126145285A>G , CM000673.1:g.126145285A>G	GRCh37
NC_000011.8:g.125650495A>G	NCBI36
NG_028029.1:g.11351A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000525083.6:n.1178A>G
ENST00000532101.6:n.797A>G
ENST00000532125.2:c.692A>G	ENSP00000434178.2:p.Gln231Arg
ENST00000533839.6:c.86-404A>G	ENSP00000509952.1:n.86-404A>G
ENST00000534011.6:n.987A>G
ENST00000685484.1:c.695A>G	ENSP00000510622.1:p.Gln232Arg
ENST00000685601.1:c.695A>G	ENSP00000510603.1:p.Gln232Arg
ENST00000685765.1:c.695A>G	ENSP00000509991.1:p.Gln232Arg
ENST00000685844.1:c.*232A>G	ENSP00000509820.1:n.*232A>G
ENST00000685857.1:n.1434A>G
ENST00000686242.1:c.494A>G	ENSP00000508950.1:n.494A>G
ENST00000686888.1:c.*262A>G	ENSP00000509619.1:n.*262A>G
ENST00000687699.1:c.819A>G	ENSP00000508878.1:n.819A>G
ENST00000687786.1:n.2131A>G
ENST00000688100.1:n.1616A>G
ENST00000688588.1:c.695A>G	ENSP00000510802.1:p.Gln232Arg
ENST00000688927.1:n.2906A>G
ENST00000689283.1:c.*358A>G	ENSP00000509050.1:n.*358A>G
ENST00000689477.1:c.*588A>G	ENSP00000508945.1:n.*588A>G
ENST00000689765.1:c.*188A>G	ENSP00000509625.1:n.*188A>G
ENST00000690512.1:c.*546A>G	ENSP00000509793.1:n.*546A>G
ENST00000692039.1:c.*493A>G	ENSP00000508821.1:n.*493A>G
ENST00000692336.1:c.719A>G	ENSP00000508540.1:p.Gln240Arg
ENST00000693133.1:n.1175A>G
ENST00000263578.10:c.695A>G MANE Select	ENSP00000263578.5:p.Gln232Arg
ENST00000263578.9:c.695A>G	ENSP00000263578.5:p.Gln232Arg
ENST00000525083.5:n.415A>G
ENST00000525770.5:c.*327A>G	ENSP00000434739.1:n.*327A>G
ENST00000527004.5:c.*39A>G	ENSP00000436374.1:n.*39A>G
ENST00000530642.1:n.1477A>G
ENST00000532101.5:n.918A>G
ENST00000532125.1:c.653A>G	ENSP00000434178.1:p.Gln218Arg
ENST00000533395.5:n.428A>G
ENST00000533839.5:n.238-404A>G
ENST00000534011.5:n.747A>G
ENST00000534315.5:n.1007A>G
NM_017547.3:c.695A>G	NP_060017.1:p.Gln232Arg
NR_037647.1:n.641A>G
NR_037648.1:n.881A>G
XM_006718879.2:c.185A>G	XP_006718942.1:p.Gln62Arg
XM_006718880.2:c.62A>G	XP_006718943.1:p.Gln21Arg
XM_006718881.2:c.62A>G	XP_006718944.1:p.Gln21Arg
XM_011542895.1:c.185A>G	XP_011541197.1:p.Gln62Arg
XM_011542896.1:c.185A>G	XP_011541198.1:p.Gln62Arg
XM_006718879.3:c.185A>G	XP_006718942.1:p.Gln62Arg
XM_006718881.3:c.62A>G	XP_006718944.1:p.Gln21Arg
XM_011542895.2:c.185A>G	XP_011541197.1:p.Gln62Arg
XM_011542896.2:c.185A>G	XP_011541198.1:p.Gln62Arg
XM_017018000.2:c.695A>G	XP_016873489.1:p.Gln232Arg
XM_017018001.1:c.185A>G	XP_016873490.1:p.Gln62Arg
XM_017018002.1:c.185A>G	XP_016873491.1:p.Gln62Arg
XM_017018003.2:c.62A>G	XP_016873492.1:p.Gln21Arg
XM_017018004.1:c.62A>G	XP_016873493.1:p.Gln21Arg
XM_017018005.1:c.62A>G	XP_016873494.1:p.Gln21Arg
XM_017018006.2:c.62A>G	XP_016873495.1:p.Gln21Arg
NM_017547.4:c.695A>G MANE Select	NP_060017.1:p.Gln232Arg
NR_037647.2:n.527A>G
NR_037648.2:n.872A>G