Canonical Allele Identifier: CA383229928

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126144857A>T (hg19) ; chr11:g.126274962A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274962A>T , CM000673.2:g.126274962A>T	GRCh38
NC_000011.9:g.126144857A>T , CM000673.1:g.126144857A>T	GRCh37
NC_000011.8:g.125650067A>T	NCBI36
NG_028029.1:g.10923A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.750A>T
ENST00000532101.6:n.734-365A>T
ENST00000532125.2:c.569A>T	ENSP00000434178.2:p.Asp190Val
ENST00000533839.6:c.86-832A>T	ENSP00000509952.1:n.86-832A>T
ENST00000534011.6:n.864A>T
ENST00000685484.1:c.572A>T	ENSP00000510622.1:p.Asp191Val
ENST00000685601.1:c.572A>T	ENSP00000510603.1:p.Asp191Val
ENST00000685765.1:c.572A>T	ENSP00000509991.1:p.Asp191Val
ENST00000685844.1:c.*169-365A>T	ENSP00000509820.1:n.*169-365A>T
ENST00000685857.1:n.1006A>T
ENST00000686242.1:c.371A>T	ENSP00000508950.1:n.371A>T
ENST00000686888.1:c.*139A>T	ENSP00000509619.1:n.*139A>T
ENST00000687699.1:c.696A>T	ENSP00000508878.1:n.696A>T
ENST00000687786.1:n.2068-365A>T
ENST00000688100.1:n.1493A>T
ENST00000688588.1:c.572A>T	ENSP00000510802.1:p.Asp191Val
ENST00000688927.1:n.2478A>T
ENST00000689283.1:c.*235A>T	ENSP00000509050.1:n.*235A>T
ENST00000689477.1:c.*465A>T	ENSP00000508945.1:n.*465A>T
ENST00000689765.1:c.*169-409A>T	ENSP00000509625.1:n.*169-409A>T
ENST00000690512.1:c.*423A>T	ENSP00000509793.1:n.*423A>T
ENST00000692039.1:c.*370A>T	ENSP00000508821.1:n.*370A>T
ENST00000692336.1:c.596A>T	ENSP00000508540.1:p.Asp199Val
ENST00000693133.1:n.747A>T
ENST00000263578.10:c.572A>T MANE Select	ENSP00000263578.5:p.Asp191Val
ENST00000263578.9:c.572A>T	ENSP00000263578.5:p.Asp191Val
ENST00000524751.5:n.508A>T
ENST00000525083.5:n.352-365A>T
ENST00000525770.5:c.*204A>T	ENSP00000434739.1:n.*204A>T
ENST00000526366.5:n.503A>T
ENST00000527004.5:c.534-365A>T	ENSP00000436374.1:n.534-365A>T
ENST00000527875.1:n.402A>T
ENST00000530642.1:n.1049A>T
ENST00000532101.5:n.795A>T
ENST00000532125.1:c.530A>T	ENSP00000434178.1:p.Asp177Val
ENST00000533395.5:n.365-365A>T
ENST00000533839.5:n.238-832A>T
ENST00000534011.5:n.624A>T
ENST00000534315.5:n.944-365A>T
NM_017547.3:c.572A>T	NP_060017.1:p.Asp191Val
NR_037647.1:n.518A>T
NR_037648.1:n.758A>T
XM_006718879.2:c.62A>T	XP_006718942.1:p.Asp21Val
XM_006718880.2:c.-2-365A>T	XP_006718943.1:n.-2-365A>T
XM_006718881.2:c.-2-365A>T	XP_006718944.1:n.-2-365A>T
XM_011542895.1:c.62A>T	XP_011541197.1:p.Asp21Val
XM_011542896.1:c.62A>T	XP_011541198.1:p.Asp21Val
XM_006718879.3:c.62A>T	XP_006718942.1:p.Asp21Val
XM_006718881.3:c.-2-365A>T	XP_006718944.1:n.-2-365A>T
XM_011542895.2:c.62A>T	XP_011541197.1:p.Asp21Val
XM_011542896.2:c.62A>T	XP_011541198.1:p.Asp21Val
XM_017018000.2:c.572A>T	XP_016873489.1:p.Asp191Val
XM_017018001.1:c.62A>T	XP_016873490.1:p.Asp21Val
XM_017018002.1:c.62A>T	XP_016873491.1:p.Asp21Val
XM_017018003.2:c.-2-365A>T	XP_016873492.1:n.-2-365A>T
XM_017018004.1:c.-2-365A>T	XP_016873493.1:n.-2-365A>T
XM_017018005.1:c.-2-365A>T	XP_016873494.1:n.-2-365A>T
XM_017018006.2:c.-2-365A>T	XP_016873495.1:n.-2-365A>T
NM_017547.4:c.572A>T MANE Select	NP_060017.1:p.Asp191Val
NR_037647.2:n.404A>T
NR_037648.2:n.749A>T