Canonical Allele Identifier: CA477515179

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126144852T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274957T>G , CM000673.2:g.126274957T>G	GRCh38
NC_000011.9:g.126144852T>G , CM000673.1:g.126144852T>G	GRCh37
NC_000011.8:g.125650062T>G	NCBI36
NG_028029.1:g.10918T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.745T>G
ENST00000532101.6:n.734-370T>G
ENST00000532125.2:c.564T>G	ENSP00000434178.2:p.Ser188=
ENST00000533839.6:c.86-837T>G	ENSP00000509952.1:n.86-837T>G
ENST00000534011.6:n.859T>G
ENST00000685484.1:c.567T>G	ENSP00000510622.1:p.Ser189=
ENST00000685601.1:c.567T>G	ENSP00000510603.1:p.Ser189=
ENST00000685765.1:c.567T>G	ENSP00000509991.1:p.Ser189=
ENST00000685844.1:c.*169-370T>G	ENSP00000509820.1:n.*169-370T>G
ENST00000685857.1:n.1001T>G
ENST00000686242.1:c.366T>G	ENSP00000508950.1:n.366T>G
ENST00000686888.1:c.*134T>G	ENSP00000509619.1:n.*134T>G
ENST00000687699.1:c.691T>G	ENSP00000508878.1:n.691T>G
ENST00000687786.1:n.2068-370T>G
ENST00000688100.1:n.1488T>G
ENST00000688588.1:c.567T>G	ENSP00000510802.1:p.Ser189=
ENST00000688927.1:n.2473T>G
ENST00000689283.1:c.*230T>G	ENSP00000509050.1:n.*230T>G
ENST00000689477.1:c.*460T>G	ENSP00000508945.1:n.*460T>G
ENST00000689765.1:c.*169-414T>G	ENSP00000509625.1:n.*169-414T>G
ENST00000690512.1:c.*418T>G	ENSP00000509793.1:n.*418T>G
ENST00000692039.1:c.*365T>G	ENSP00000508821.1:n.*365T>G
ENST00000692336.1:c.591T>G	ENSP00000508540.1:p.Ser197=
ENST00000693133.1:n.742T>G
ENST00000263578.10:c.567T>G MANE Select	ENSP00000263578.5:p.Ser189=
ENST00000263578.9:c.567T>G	ENSP00000263578.5:p.Ser189=
ENST00000524751.5:n.503T>G
ENST00000525083.5:n.352-370T>G
ENST00000525770.5:c.*199T>G	ENSP00000434739.1:n.*199T>G
ENST00000526366.5:n.498T>G
ENST00000527004.5:c.534-370T>G	ENSP00000436374.1:n.534-370T>G
ENST00000527875.1:n.397T>G
ENST00000530642.1:n.1044T>G
ENST00000532101.5:n.790T>G
ENST00000532125.1:c.525T>G	ENSP00000434178.1:p.Ser175=
ENST00000533395.5:n.365-370T>G
ENST00000533839.5:n.238-837T>G
ENST00000534011.5:n.619T>G
ENST00000534315.5:n.944-370T>G
NM_017547.3:c.567T>G	NP_060017.1:p.Ser189=
NR_037647.1:n.513T>G
NR_037648.1:n.753T>G
XM_006718879.2:c.57T>G	XP_006718942.1:p.Ser19=
XM_006718880.2:c.-2-370T>G	XP_006718943.1:n.-2-370T>G
XM_006718881.2:c.-2-370T>G	XP_006718944.1:n.-2-370T>G
XM_011542895.1:c.57T>G	XP_011541197.1:p.Ser19=
XM_011542896.1:c.57T>G	XP_011541198.1:p.Ser19=
XM_006718879.3:c.57T>G	XP_006718942.1:p.Ser19=
XM_006718881.3:c.-2-370T>G	XP_006718944.1:n.-2-370T>G
XM_011542895.2:c.57T>G	XP_011541197.1:p.Ser19=
XM_011542896.2:c.57T>G	XP_011541198.1:p.Ser19=
XM_017018000.2:c.567T>G	XP_016873489.1:p.Ser189=
XM_017018001.1:c.57T>G	XP_016873490.1:p.Ser19=
XM_017018002.1:c.57T>G	XP_016873491.1:p.Ser19=
XM_017018003.2:c.-2-370T>G	XP_016873492.1:n.-2-370T>G
XM_017018004.1:c.-2-370T>G	XP_016873493.1:n.-2-370T>G
XM_017018005.1:c.-2-370T>G	XP_016873494.1:n.-2-370T>G
XM_017018006.2:c.-2-370T>G	XP_016873495.1:n.-2-370T>G
NM_017547.4:c.567T>G MANE Select	NP_060017.1:p.Ser189=
NR_037647.2:n.399T>G
NR_037648.2:n.744T>G