Canonical Allele Identifier: CA383230041

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126144910T>G (hg19) ; chr11:g.126275015T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275015T>G , CM000673.2:g.126275015T>G	GRCh38
NC_000011.9:g.126144910T>G , CM000673.1:g.126144910T>G	GRCh37
NC_000011.8:g.125650120T>G	NCBI36
NG_028029.1:g.10976T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.803T>G
ENST00000532101.6:n.734-312T>G
ENST00000532125.2:c.622T>G	ENSP00000434178.2:p.Ser208Ala
ENST00000533839.6:c.86-779T>G	ENSP00000509952.1:n.86-779T>G
ENST00000534011.6:n.917T>G
ENST00000685484.1:c.625T>G	ENSP00000510622.1:p.Ser209Ala
ENST00000685601.1:c.625T>G	ENSP00000510603.1:p.Ser209Ala
ENST00000685765.1:c.625T>G	ENSP00000509991.1:p.Ser209Ala
ENST00000685844.1:c.*169-312T>G	ENSP00000509820.1:n.*169-312T>G
ENST00000685857.1:n.1059T>G
ENST00000686242.1:c.424T>G	ENSP00000508950.1:n.424T>G
ENST00000686888.1:c.*192T>G	ENSP00000509619.1:n.*192T>G
ENST00000687699.1:c.749T>G	ENSP00000508878.1:n.749T>G
ENST00000687786.1:n.2068-312T>G
ENST00000688100.1:n.1546T>G
ENST00000688588.1:c.625T>G	ENSP00000510802.1:p.Ser209Ala
ENST00000688927.1:n.2531T>G
ENST00000689283.1:c.*288T>G	ENSP00000509050.1:n.*288T>G
ENST00000689477.1:c.*518T>G	ENSP00000508945.1:n.*518T>G
ENST00000689765.1:c.*169-356T>G	ENSP00000509625.1:n.*169-356T>G
ENST00000690512.1:c.*476T>G	ENSP00000509793.1:n.*476T>G
ENST00000692039.1:c.*423T>G	ENSP00000508821.1:n.*423T>G
ENST00000692336.1:c.649T>G	ENSP00000508540.1:p.Ser217Ala
ENST00000693133.1:n.800T>G
ENST00000263578.10:c.625T>G MANE Select	ENSP00000263578.5:p.Ser209Ala
ENST00000263578.9:c.625T>G	ENSP00000263578.5:p.Ser209Ala
ENST00000524751.5:n.561T>G
ENST00000525083.5:n.352-312T>G
ENST00000525770.5:c.*257T>G	ENSP00000434739.1:n.*257T>G
ENST00000527004.5:c.534-312T>G	ENSP00000436374.1:n.534-312T>G
ENST00000527875.1:n.455T>G
ENST00000530642.1:n.1102T>G
ENST00000532101.5:n.848T>G
ENST00000532125.1:c.583T>G	ENSP00000434178.1:p.Ser195Ala
ENST00000533395.5:n.365-312T>G
ENST00000533839.5:n.238-779T>G
ENST00000534011.5:n.677T>G
ENST00000534315.5:n.944-312T>G
NM_017547.3:c.625T>G	NP_060017.1:p.Ser209Ala
NR_037647.1:n.571T>G
NR_037648.1:n.811T>G
XM_006718879.2:c.115T>G	XP_006718942.1:p.Ser39Ala
XM_006718880.2:c.-2-312T>G	XP_006718943.1:n.-2-312T>G
XM_006718881.2:c.-2-312T>G	XP_006718944.1:n.-2-312T>G
XM_011542895.1:c.115T>G	XP_011541197.1:p.Ser39Ala
XM_011542896.1:c.115T>G	XP_011541198.1:p.Ser39Ala
XM_006718879.3:c.115T>G	XP_006718942.1:p.Ser39Ala
XM_006718881.3:c.-2-312T>G	XP_006718944.1:n.-2-312T>G
XM_011542895.2:c.115T>G	XP_011541197.1:p.Ser39Ala
XM_011542896.2:c.115T>G	XP_011541198.1:p.Ser39Ala
XM_017018000.2:c.625T>G	XP_016873489.1:p.Ser209Ala
XM_017018001.1:c.115T>G	XP_016873490.1:p.Ser39Ala
XM_017018002.1:c.115T>G	XP_016873491.1:p.Ser39Ala
XM_017018003.2:c.-2-312T>G	XP_016873492.1:n.-2-312T>G
XM_017018004.1:c.-2-312T>G	XP_016873493.1:n.-2-312T>G
XM_017018005.1:c.-2-312T>G	XP_016873494.1:n.-2-312T>G
XM_017018006.2:c.-2-312T>G	XP_016873495.1:n.-2-312T>G
NM_017547.4:c.625T>G MANE Select	NP_060017.1:p.Ser209Ala
NR_037647.2:n.457T>G
NR_037648.2:n.802T>G