Canonical Allele Identifier: CA383230156

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145258T>G (hg19) ; chr11:g.126275363T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275363T>G , CM000673.2:g.126275363T>G	GRCh38
NC_000011.9:g.126145258T>G , CM000673.1:g.126145258T>G	GRCh37
NC_000011.8:g.125650468T>G	NCBI36
NG_028029.1:g.11324T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1151T>G
ENST00000532101.6:n.770T>G
ENST00000532125.2:c.665T>G	ENSP00000434178.2:p.Leu222Arg
ENST00000533839.6:c.86-431T>G	ENSP00000509952.1:n.86-431T>G
ENST00000534011.6:n.960T>G
ENST00000685484.1:c.668T>G	ENSP00000510622.1:p.Leu223Arg
ENST00000685601.1:c.668T>G	ENSP00000510603.1:p.Leu223Arg
ENST00000685765.1:c.668T>G	ENSP00000509991.1:p.Leu223Arg
ENST00000685844.1:c.*205T>G	ENSP00000509820.1:n.*205T>G
ENST00000685857.1:n.1407T>G
ENST00000686242.1:c.467T>G	ENSP00000508950.1:n.467T>G
ENST00000686888.1:c.*235T>G	ENSP00000509619.1:n.*235T>G
ENST00000687699.1:c.792T>G	ENSP00000508878.1:n.792T>G
ENST00000687786.1:n.2104T>G
ENST00000688100.1:n.1589T>G
ENST00000688588.1:c.668T>G	ENSP00000510802.1:p.Leu223Arg
ENST00000688927.1:n.2879T>G
ENST00000689283.1:c.*331T>G	ENSP00000509050.1:n.*331T>G
ENST00000689477.1:c.*561T>G	ENSP00000508945.1:n.*561T>G
ENST00000689765.1:c.*169-8T>G	ENSP00000509625.1:n.*169-8T>G
ENST00000690512.1:c.*519T>G	ENSP00000509793.1:n.*519T>G
ENST00000692039.1:c.*466T>G	ENSP00000508821.1:n.*466T>G
ENST00000692336.1:c.692T>G	ENSP00000508540.1:p.Leu231Arg
ENST00000693133.1:n.1148T>G
ENST00000263578.10:c.668T>G MANE Select	ENSP00000263578.5:p.Leu223Arg
ENST00000263578.9:c.668T>G	ENSP00000263578.5:p.Leu223Arg
ENST00000525083.5:n.388T>G
ENST00000525770.5:c.*300T>G	ENSP00000434739.1:n.*300T>G
ENST00000527004.5:c.*12T>G	ENSP00000436374.1:n.*12T>G
ENST00000530642.1:n.1450T>G
ENST00000532101.5:n.891T>G
ENST00000532125.1:c.626T>G	ENSP00000434178.1:p.Leu209Arg
ENST00000533395.5:n.401T>G
ENST00000533839.5:n.238-431T>G
ENST00000534011.5:n.720T>G
ENST00000534315.5:n.980T>G
NM_017547.3:c.668T>G	NP_060017.1:p.Leu223Arg
NR_037647.1:n.614T>G
NR_037648.1:n.854T>G
XM_006718879.2:c.158T>G	XP_006718942.1:p.Leu53Arg
XM_006718880.2:c.35T>G	XP_006718943.1:p.Leu12Arg
XM_006718881.2:c.35T>G	XP_006718944.1:p.Leu12Arg
XM_011542895.1:c.158T>G	XP_011541197.1:p.Leu53Arg
XM_011542896.1:c.158T>G	XP_011541198.1:p.Leu53Arg
XM_006718879.3:c.158T>G	XP_006718942.1:p.Leu53Arg
XM_006718881.3:c.35T>G	XP_006718944.1:p.Leu12Arg
XM_011542895.2:c.158T>G	XP_011541197.1:p.Leu53Arg
XM_011542896.2:c.158T>G	XP_011541198.1:p.Leu53Arg
XM_017018000.2:c.668T>G	XP_016873489.1:p.Leu223Arg
XM_017018001.1:c.158T>G	XP_016873490.1:p.Leu53Arg
XM_017018002.1:c.158T>G	XP_016873491.1:p.Leu53Arg
XM_017018003.2:c.35T>G	XP_016873492.1:p.Leu12Arg
XM_017018004.1:c.35T>G	XP_016873493.1:p.Leu12Arg
XM_017018005.1:c.35T>G	XP_016873494.1:p.Leu12Arg
XM_017018006.2:c.35T>G	XP_016873495.1:p.Leu12Arg
NM_017547.4:c.668T>G MANE Select	NP_060017.1:p.Leu223Arg
NR_037647.2:n.500T>G
NR_037648.2:n.845T>G