Canonical Allele Identifier: CA383229955

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126144871A>G (hg19) ; chr11:g.126274976A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274976A>G , CM000673.2:g.126274976A>G	GRCh38
NC_000011.9:g.126144871A>G , CM000673.1:g.126144871A>G	GRCh37
NC_000011.8:g.125650081A>G	NCBI36
NG_028029.1:g.10937A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.764A>G
ENST00000532101.6:n.734-351A>G
ENST00000532125.2:c.583A>G	ENSP00000434178.2:p.Lys195Glu
ENST00000533839.6:c.86-818A>G	ENSP00000509952.1:n.86-818A>G
ENST00000534011.6:n.878A>G
ENST00000685484.1:c.586A>G	ENSP00000510622.1:p.Lys196Glu
ENST00000685601.1:c.586A>G	ENSP00000510603.1:p.Lys196Glu
ENST00000685765.1:c.586A>G	ENSP00000509991.1:p.Lys196Glu
ENST00000685844.1:c.*169-351A>G	ENSP00000509820.1:n.*169-351A>G
ENST00000685857.1:n.1020A>G
ENST00000686242.1:c.385A>G	ENSP00000508950.1:n.385A>G
ENST00000686888.1:c.*153A>G	ENSP00000509619.1:n.*153A>G
ENST00000687699.1:c.710A>G	ENSP00000508878.1:n.710A>G
ENST00000687786.1:n.2068-351A>G
ENST00000688100.1:n.1507A>G
ENST00000688588.1:c.586A>G	ENSP00000510802.1:p.Lys196Glu
ENST00000688927.1:n.2492A>G
ENST00000689283.1:c.*249A>G	ENSP00000509050.1:n.*249A>G
ENST00000689477.1:c.*479A>G	ENSP00000508945.1:n.*479A>G
ENST00000689765.1:c.*169-395A>G	ENSP00000509625.1:n.*169-395A>G
ENST00000690512.1:c.*437A>G	ENSP00000509793.1:n.*437A>G
ENST00000692039.1:c.*384A>G	ENSP00000508821.1:n.*384A>G
ENST00000692336.1:c.610A>G	ENSP00000508540.1:p.Lys204Glu
ENST00000693133.1:n.761A>G
ENST00000263578.10:c.586A>G MANE Select	ENSP00000263578.5:p.Lys196Glu
ENST00000263578.9:c.586A>G	ENSP00000263578.5:p.Lys196Glu
ENST00000524751.5:n.522A>G
ENST00000525083.5:n.352-351A>G
ENST00000525770.5:c.*218A>G	ENSP00000434739.1:n.*218A>G
ENST00000526366.5:n.517A>G
ENST00000527004.5:c.534-351A>G	ENSP00000436374.1:n.534-351A>G
ENST00000527875.1:n.416A>G
ENST00000530642.1:n.1063A>G
ENST00000532101.5:n.809A>G
ENST00000532125.1:c.544A>G	ENSP00000434178.1:p.Lys182Glu
ENST00000533395.5:n.365-351A>G
ENST00000533839.5:n.238-818A>G
ENST00000534011.5:n.638A>G
ENST00000534315.5:n.944-351A>G
NM_017547.3:c.586A>G	NP_060017.1:p.Lys196Glu
NR_037647.1:n.532A>G
NR_037648.1:n.772A>G
XM_006718879.2:c.76A>G	XP_006718942.1:p.Lys26Glu
XM_006718880.2:c.-2-351A>G	XP_006718943.1:n.-2-351A>G
XM_006718881.2:c.-2-351A>G	XP_006718944.1:n.-2-351A>G
XM_011542895.1:c.76A>G	XP_011541197.1:p.Lys26Glu
XM_011542896.1:c.76A>G	XP_011541198.1:p.Lys26Glu
XM_006718879.3:c.76A>G	XP_006718942.1:p.Lys26Glu
XM_006718881.3:c.-2-351A>G	XP_006718944.1:n.-2-351A>G
XM_011542895.2:c.76A>G	XP_011541197.1:p.Lys26Glu
XM_011542896.2:c.76A>G	XP_011541198.1:p.Lys26Glu
XM_017018000.2:c.586A>G	XP_016873489.1:p.Lys196Glu
XM_017018001.1:c.76A>G	XP_016873490.1:p.Lys26Glu
XM_017018002.1:c.76A>G	XP_016873491.1:p.Lys26Glu
XM_017018003.2:c.-2-351A>G	XP_016873492.1:n.-2-351A>G
XM_017018004.1:c.-2-351A>G	XP_016873493.1:n.-2-351A>G
XM_017018005.1:c.-2-351A>G	XP_016873494.1:n.-2-351A>G
XM_017018006.2:c.-2-351A>G	XP_016873495.1:n.-2-351A>G
NM_017547.4:c.586A>G MANE Select	NP_060017.1:p.Lys196Glu
NR_037647.2:n.418A>G
NR_037648.2:n.763A>G