Canonical Allele Identifier: CA383229962

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126144874T>G (hg19) ; chr11:g.126274979T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274979T>G , CM000673.2:g.126274979T>G	GRCh38
NC_000011.9:g.126144874T>G , CM000673.1:g.126144874T>G	GRCh37
NC_000011.8:g.125650084T>G	NCBI36
NG_028029.1:g.10940T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.767T>G
ENST00000532101.6:n.734-348T>G
ENST00000532125.2:c.586T>G	ENSP00000434178.2:p.Phe196Val
ENST00000533839.6:c.86-815T>G	ENSP00000509952.1:n.86-815T>G
ENST00000534011.6:n.881T>G
ENST00000685484.1:c.589T>G	ENSP00000510622.1:p.Phe197Val
ENST00000685601.1:c.589T>G	ENSP00000510603.1:p.Phe197Val
ENST00000685765.1:c.589T>G	ENSP00000509991.1:p.Phe197Val
ENST00000685844.1:c.*169-348T>G	ENSP00000509820.1:n.*169-348T>G
ENST00000685857.1:n.1023T>G
ENST00000686242.1:c.388T>G	ENSP00000508950.1:n.388T>G
ENST00000686888.1:c.*156T>G	ENSP00000509619.1:n.*156T>G
ENST00000687699.1:c.713T>G	ENSP00000508878.1:n.713T>G
ENST00000687786.1:n.2068-348T>G
ENST00000688100.1:n.1510T>G
ENST00000688588.1:c.589T>G	ENSP00000510802.1:p.Phe197Val
ENST00000688927.1:n.2495T>G
ENST00000689283.1:c.*252T>G	ENSP00000509050.1:n.*252T>G
ENST00000689477.1:c.*482T>G	ENSP00000508945.1:n.*482T>G
ENST00000689765.1:c.*169-392T>G	ENSP00000509625.1:n.*169-392T>G
ENST00000690512.1:c.*440T>G	ENSP00000509793.1:n.*440T>G
ENST00000692039.1:c.*387T>G	ENSP00000508821.1:n.*387T>G
ENST00000692336.1:c.613T>G	ENSP00000508540.1:p.Phe205Val
ENST00000693133.1:n.764T>G
ENST00000263578.10:c.589T>G MANE Select	ENSP00000263578.5:p.Phe197Val
ENST00000263578.9:c.589T>G	ENSP00000263578.5:p.Phe197Val
ENST00000524751.5:n.525T>G
ENST00000525083.5:n.352-348T>G
ENST00000525770.5:c.*221T>G	ENSP00000434739.1:n.*221T>G
ENST00000526366.5:n.520T>G
ENST00000527004.5:c.534-348T>G	ENSP00000436374.1:n.534-348T>G
ENST00000527875.1:n.419T>G
ENST00000530642.1:n.1066T>G
ENST00000532101.5:n.812T>G
ENST00000532125.1:c.547T>G	ENSP00000434178.1:p.Phe183Val
ENST00000533395.5:n.365-348T>G
ENST00000533839.5:n.238-815T>G
ENST00000534011.5:n.641T>G
ENST00000534315.5:n.944-348T>G
NM_017547.3:c.589T>G	NP_060017.1:p.Phe197Val
NR_037647.1:n.535T>G
NR_037648.1:n.775T>G
XM_006718879.2:c.79T>G	XP_006718942.1:p.Phe27Val
XM_006718880.2:c.-2-348T>G	XP_006718943.1:n.-2-348T>G
XM_006718881.2:c.-2-348T>G	XP_006718944.1:n.-2-348T>G
XM_011542895.1:c.79T>G	XP_011541197.1:p.Phe27Val
XM_011542896.1:c.79T>G	XP_011541198.1:p.Phe27Val
XM_006718879.3:c.79T>G	XP_006718942.1:p.Phe27Val
XM_006718881.3:c.-2-348T>G	XP_006718944.1:n.-2-348T>G
XM_011542895.2:c.79T>G	XP_011541197.1:p.Phe27Val
XM_011542896.2:c.79T>G	XP_011541198.1:p.Phe27Val
XM_017018000.2:c.589T>G	XP_016873489.1:p.Phe197Val
XM_017018001.1:c.79T>G	XP_016873490.1:p.Phe27Val
XM_017018002.1:c.79T>G	XP_016873491.1:p.Phe27Val
XM_017018003.2:c.-2-348T>G	XP_016873492.1:n.-2-348T>G
XM_017018004.1:c.-2-348T>G	XP_016873493.1:n.-2-348T>G
XM_017018005.1:c.-2-348T>G	XP_016873494.1:n.-2-348T>G
XM_017018006.2:c.-2-348T>G	XP_016873495.1:n.-2-348T>G
NM_017547.4:c.589T>G MANE Select	NP_060017.1:p.Phe197Val
NR_037647.2:n.421T>G
NR_037648.2:n.766T>G