Canonical Allele Identifier: CA383230164

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145263C>G (hg19) ; chr11:g.126275368C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275368C>G , CM000673.2:g.126275368C>G	GRCh38
NC_000011.9:g.126145263C>G , CM000673.1:g.126145263C>G	GRCh37
NC_000011.8:g.125650473C>G	NCBI36
NG_028029.1:g.11329C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1156C>G
ENST00000532101.6:n.775C>G
ENST00000532125.2:c.670C>G	ENSP00000434178.2:p.Gln224Glu
ENST00000533839.6:c.86-426C>G	ENSP00000509952.1:n.86-426C>G
ENST00000534011.6:n.965C>G
ENST00000685484.1:c.673C>G	ENSP00000510622.1:p.Gln225Glu
ENST00000685601.1:c.673C>G	ENSP00000510603.1:p.Gln225Glu
ENST00000685765.1:c.673C>G	ENSP00000509991.1:p.Gln225Glu
ENST00000685844.1:c.*210C>G	ENSP00000509820.1:n.*210C>G
ENST00000685857.1:n.1412C>G
ENST00000686242.1:c.472C>G	ENSP00000508950.1:n.472C>G
ENST00000686888.1:c.*240C>G	ENSP00000509619.1:n.*240C>G
ENST00000687699.1:c.797C>G	ENSP00000508878.1:n.797C>G
ENST00000687786.1:n.2109C>G
ENST00000688100.1:n.1594C>G
ENST00000688588.1:c.673C>G	ENSP00000510802.1:p.Gln225Glu
ENST00000688927.1:n.2884C>G
ENST00000689283.1:c.*336C>G	ENSP00000509050.1:n.*336C>G
ENST00000689477.1:c.*566C>G	ENSP00000508945.1:n.*566C>G
ENST00000689765.1:c.*169-3C>G	ENSP00000509625.1:n.*169-3C>G
ENST00000690512.1:c.*524C>G	ENSP00000509793.1:n.*524C>G
ENST00000692039.1:c.*471C>G	ENSP00000508821.1:n.*471C>G
ENST00000692336.1:c.697C>G	ENSP00000508540.1:p.Gln233Glu
ENST00000693133.1:n.1153C>G
ENST00000263578.10:c.673C>G MANE Select	ENSP00000263578.5:p.Gln225Glu
ENST00000263578.9:c.673C>G	ENSP00000263578.5:p.Gln225Glu
ENST00000525083.5:n.393C>G
ENST00000525770.5:c.*305C>G	ENSP00000434739.1:n.*305C>G
ENST00000527004.5:c.*17C>G	ENSP00000436374.1:n.*17C>G
ENST00000530642.1:n.1455C>G
ENST00000532101.5:n.896C>G
ENST00000532125.1:c.631C>G	ENSP00000434178.1:p.Gln211Glu
ENST00000533395.5:n.406C>G
ENST00000533839.5:n.238-426C>G
ENST00000534011.5:n.725C>G
ENST00000534315.5:n.985C>G
NM_017547.3:c.673C>G	NP_060017.1:p.Gln225Glu
NR_037647.1:n.619C>G
NR_037648.1:n.859C>G
XM_006718879.2:c.163C>G	XP_006718942.1:p.Gln55Glu
XM_006718880.2:c.40C>G	XP_006718943.1:p.Gln14Glu
XM_006718881.2:c.40C>G	XP_006718944.1:p.Gln14Glu
XM_011542895.1:c.163C>G	XP_011541197.1:p.Gln55Glu
XM_011542896.1:c.163C>G	XP_011541198.1:p.Gln55Glu
XM_006718879.3:c.163C>G	XP_006718942.1:p.Gln55Glu
XM_006718881.3:c.40C>G	XP_006718944.1:p.Gln14Glu
XM_011542895.2:c.163C>G	XP_011541197.1:p.Gln55Glu
XM_011542896.2:c.163C>G	XP_011541198.1:p.Gln55Glu
XM_017018000.2:c.673C>G	XP_016873489.1:p.Gln225Glu
XM_017018001.1:c.163C>G	XP_016873490.1:p.Gln55Glu
XM_017018002.1:c.163C>G	XP_016873491.1:p.Gln55Glu
XM_017018003.2:c.40C>G	XP_016873492.1:p.Gln14Glu
XM_017018004.1:c.40C>G	XP_016873493.1:p.Gln14Glu
XM_017018005.1:c.40C>G	XP_016873494.1:p.Gln14Glu
XM_017018006.2:c.40C>G	XP_016873495.1:p.Gln14Glu
NM_017547.4:c.673C>G MANE Select	NP_060017.1:p.Gln225Glu
NR_037647.2:n.505C>G
NR_037648.2:n.850C>G