Canonical Allele Identifier: CA477515362

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126144903T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275008T>A , CM000673.2:g.126275008T>A	GRCh38
NC_000011.9:g.126144903T>A , CM000673.1:g.126144903T>A	GRCh37
NC_000011.8:g.125650113T>A	NCBI36
NG_028029.1:g.10969T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.796T>A
ENST00000532101.6:n.734-319T>A
ENST00000532125.2:c.615T>A	ENSP00000434178.2:p.Ala205=
ENST00000533839.6:c.86-786T>A	ENSP00000509952.1:n.86-786T>A
ENST00000534011.6:n.910T>A
ENST00000685484.1:c.618T>A	ENSP00000510622.1:p.Ala206=
ENST00000685601.1:c.618T>A	ENSP00000510603.1:p.Ala206=
ENST00000685765.1:c.618T>A	ENSP00000509991.1:p.Ala206=
ENST00000685844.1:c.*169-319T>A	ENSP00000509820.1:n.*169-319T>A
ENST00000685857.1:n.1052T>A
ENST00000686242.1:c.417T>A	ENSP00000508950.1:n.417T>A
ENST00000686888.1:c.*185T>A	ENSP00000509619.1:n.*185T>A
ENST00000687699.1:c.742T>A	ENSP00000508878.1:n.742T>A
ENST00000687786.1:n.2068-319T>A
ENST00000688100.1:n.1539T>A
ENST00000688588.1:c.618T>A	ENSP00000510802.1:p.Ala206=
ENST00000688927.1:n.2524T>A
ENST00000689283.1:c.*281T>A	ENSP00000509050.1:n.*281T>A
ENST00000689477.1:c.*511T>A	ENSP00000508945.1:n.*511T>A
ENST00000689765.1:c.*169-363T>A	ENSP00000509625.1:n.*169-363T>A
ENST00000690512.1:c.*469T>A	ENSP00000509793.1:n.*469T>A
ENST00000692039.1:c.*416T>A	ENSP00000508821.1:n.*416T>A
ENST00000692336.1:c.642T>A	ENSP00000508540.1:p.Ala214=
ENST00000693133.1:n.793T>A
ENST00000263578.10:c.618T>A MANE Select	ENSP00000263578.5:p.Ala206=
ENST00000263578.9:c.618T>A	ENSP00000263578.5:p.Ala206=
ENST00000524751.5:n.554T>A
ENST00000525083.5:n.352-319T>A
ENST00000525770.5:c.*250T>A	ENSP00000434739.1:n.*250T>A
ENST00000526366.5:n.549T>A
ENST00000527004.5:c.534-319T>A	ENSP00000436374.1:n.534-319T>A
ENST00000527875.1:n.448T>A
ENST00000530642.1:n.1095T>A
ENST00000532101.5:n.841T>A
ENST00000532125.1:c.576T>A	ENSP00000434178.1:p.Ala192=
ENST00000533395.5:n.365-319T>A
ENST00000533839.5:n.238-786T>A
ENST00000534011.5:n.670T>A
ENST00000534315.5:n.944-319T>A
NM_017547.3:c.618T>A	NP_060017.1:p.Ala206=
NR_037647.1:n.564T>A
NR_037648.1:n.804T>A
XM_006718879.2:c.108T>A	XP_006718942.1:p.Ala36=
XM_006718880.2:c.-2-319T>A	XP_006718943.1:n.-2-319T>A
XM_006718881.2:c.-2-319T>A	XP_006718944.1:n.-2-319T>A
XM_011542895.1:c.108T>A	XP_011541197.1:p.Ala36=
XM_011542896.1:c.108T>A	XP_011541198.1:p.Ala36=
XM_006718879.3:c.108T>A	XP_006718942.1:p.Ala36=
XM_006718881.3:c.-2-319T>A	XP_006718944.1:n.-2-319T>A
XM_011542895.2:c.108T>A	XP_011541197.1:p.Ala36=
XM_011542896.2:c.108T>A	XP_011541198.1:p.Ala36=
XM_017018000.2:c.618T>A	XP_016873489.1:p.Ala206=
XM_017018001.1:c.108T>A	XP_016873490.1:p.Ala36=
XM_017018002.1:c.108T>A	XP_016873491.1:p.Ala36=
XM_017018003.2:c.-2-319T>A	XP_016873492.1:n.-2-319T>A
XM_017018004.1:c.-2-319T>A	XP_016873493.1:n.-2-319T>A
XM_017018005.1:c.-2-319T>A	XP_016873494.1:n.-2-319T>A
XM_017018006.2:c.-2-319T>A	XP_016873495.1:n.-2-319T>A
NM_017547.4:c.618T>A MANE Select	NP_060017.1:p.Ala206=
NR_037647.2:n.450T>A
NR_037648.2:n.795T>A