Canonical Allele Identifier: CA383230185

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145275C>G (hg19) ; chr11:g.126275380C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275380C>G , CM000673.2:g.126275380C>G	GRCh38
NC_000011.9:g.126145275C>G , CM000673.1:g.126145275C>G	GRCh37
NC_000011.8:g.125650485C>G	NCBI36
NG_028029.1:g.11341C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1168C>G
ENST00000532101.6:n.787C>G
ENST00000532125.2:c.682C>G	ENSP00000434178.2:p.Arg228Gly
ENST00000533839.6:c.86-414C>G	ENSP00000509952.1:n.86-414C>G
ENST00000534011.6:n.977C>G
ENST00000685484.1:c.685C>G	ENSP00000510622.1:p.Arg229Gly
ENST00000685601.1:c.685C>G	ENSP00000510603.1:p.Arg229Gly
ENST00000685765.1:c.685C>G	ENSP00000509991.1:p.Arg229Gly
ENST00000685844.1:c.*222C>G	ENSP00000509820.1:n.*222C>G
ENST00000685857.1:n.1424C>G
ENST00000686242.1:c.484C>G	ENSP00000508950.1:n.484C>G
ENST00000686888.1:c.*252C>G	ENSP00000509619.1:n.*252C>G
ENST00000687699.1:c.809C>G	ENSP00000508878.1:n.809C>G
ENST00000687786.1:n.2121C>G
ENST00000688100.1:n.1606C>G
ENST00000688588.1:c.685C>G	ENSP00000510802.1:p.Arg229Gly
ENST00000688927.1:n.2896C>G
ENST00000689283.1:c.*348C>G	ENSP00000509050.1:n.*348C>G
ENST00000689477.1:c.*578C>G	ENSP00000508945.1:n.*578C>G
ENST00000689765.1:c.*178C>G	ENSP00000509625.1:n.*178C>G
ENST00000690512.1:c.*536C>G	ENSP00000509793.1:n.*536C>G
ENST00000692039.1:c.*483C>G	ENSP00000508821.1:n.*483C>G
ENST00000692336.1:c.709C>G	ENSP00000508540.1:p.Arg237Gly
ENST00000693133.1:n.1165C>G
ENST00000263578.10:c.685C>G MANE Select	ENSP00000263578.5:p.Arg229Gly
ENST00000263578.9:c.685C>G	ENSP00000263578.5:p.Arg229Gly
ENST00000525083.5:n.405C>G
ENST00000525770.5:c.*317C>G	ENSP00000434739.1:n.*317C>G
ENST00000527004.5:c.*29C>G	ENSP00000436374.1:n.*29C>G
ENST00000530642.1:n.1467C>G
ENST00000532101.5:n.908C>G
ENST00000532125.1:c.643C>G	ENSP00000434178.1:p.Arg215Gly
ENST00000533395.5:n.418C>G
ENST00000533839.5:n.238-414C>G
ENST00000534011.5:n.737C>G
ENST00000534315.5:n.997C>G
NM_017547.3:c.685C>G	NP_060017.1:p.Arg229Gly
NR_037647.1:n.631C>G
NR_037648.1:n.871C>G
XM_006718879.2:c.175C>G	XP_006718942.1:p.Arg59Gly
XM_006718880.2:c.52C>G	XP_006718943.1:p.Arg18Gly
XM_006718881.2:c.52C>G	XP_006718944.1:p.Arg18Gly
XM_011542895.1:c.175C>G	XP_011541197.1:p.Arg59Gly
XM_011542896.1:c.175C>G	XP_011541198.1:p.Arg59Gly
XM_006718879.3:c.175C>G	XP_006718942.1:p.Arg59Gly
XM_006718881.3:c.52C>G	XP_006718944.1:p.Arg18Gly
XM_011542895.2:c.175C>G	XP_011541197.1:p.Arg59Gly
XM_011542896.2:c.175C>G	XP_011541198.1:p.Arg59Gly
XM_017018000.2:c.685C>G	XP_016873489.1:p.Arg229Gly
XM_017018001.1:c.175C>G	XP_016873490.1:p.Arg59Gly
XM_017018002.1:c.175C>G	XP_016873491.1:p.Arg59Gly
XM_017018003.2:c.52C>G	XP_016873492.1:p.Arg18Gly
XM_017018004.1:c.52C>G	XP_016873493.1:p.Arg18Gly
XM_017018005.1:c.52C>G	XP_016873494.1:p.Arg18Gly
XM_017018006.2:c.52C>G	XP_016873495.1:p.Arg18Gly
NM_017547.4:c.685C>G MANE Select	NP_060017.1:p.Arg229Gly
NR_037647.2:n.517C>G
NR_037648.2:n.862C>G