Canonical Allele Identifier: CA383229874

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126144830G>C (hg19) ; chr11:g.126274935G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274935G>C , CM000673.2:g.126274935G>C	GRCh38
NC_000011.9:g.126144830G>C , CM000673.1:g.126144830G>C	GRCh37
NC_000011.8:g.125650040G>C	NCBI36
NG_028029.1:g.10896G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.723G>C
ENST00000532101.6:n.734-392G>C
ENST00000532125.2:c.542G>C	ENSP00000434178.2:p.Gly181Ala
ENST00000533839.6:c.86-859G>C	ENSP00000509952.1:n.86-859G>C
ENST00000534011.6:n.837G>C
ENST00000685484.1:c.545G>C	ENSP00000510622.1:p.Gly182Ala
ENST00000685601.1:c.545G>C	ENSP00000510603.1:p.Gly182Ala
ENST00000685765.1:c.545G>C	ENSP00000509991.1:p.Gly182Ala
ENST00000685844.1:c.*169-392G>C	ENSP00000509820.1:n.*169-392G>C
ENST00000685857.1:n.979G>C
ENST00000686242.1:c.344G>C	ENSP00000508950.1:n.344G>C
ENST00000686888.1:c.*112G>C	ENSP00000509619.1:n.*112G>C
ENST00000687699.1:c.669G>C	ENSP00000508878.1:n.669G>C
ENST00000687786.1:n.2068-392G>C
ENST00000688100.1:n.1466G>C
ENST00000688588.1:c.545G>C	ENSP00000510802.1:p.Gly182Ala
ENST00000688927.1:n.2451G>C
ENST00000689283.1:c.*208G>C	ENSP00000509050.1:n.*208G>C
ENST00000689477.1:c.*438G>C	ENSP00000508945.1:n.*438G>C
ENST00000689765.1:c.*169-436G>C	ENSP00000509625.1:n.*169-436G>C
ENST00000690512.1:c.*396G>C	ENSP00000509793.1:n.*396G>C
ENST00000692039.1:c.*343G>C	ENSP00000508821.1:n.*343G>C
ENST00000692336.1:c.569G>C	ENSP00000508540.1:p.Gly190Ala
ENST00000693133.1:n.720G>C
ENST00000263578.10:c.545G>C MANE Select	ENSP00000263578.5:p.Gly182Ala
ENST00000263578.9:c.545G>C	ENSP00000263578.5:p.Gly182Ala
ENST00000524751.5:n.481G>C
ENST00000525083.5:n.352-392G>C
ENST00000525770.5:c.*177G>C	ENSP00000434739.1:n.*177G>C
ENST00000526366.5:n.476G>C
ENST00000527004.5:c.534-392G>C	ENSP00000436374.1:n.534-392G>C
ENST00000527875.1:n.375G>C
ENST00000530642.1:n.1022G>C
ENST00000532101.5:n.768G>C
ENST00000532125.1:c.503G>C	ENSP00000434178.1:p.Gly168Ala
ENST00000533395.5:n.365-392G>C
ENST00000533839.5:n.238-859G>C
ENST00000534011.5:n.597G>C
ENST00000534315.5:n.944-392G>C
NM_017547.3:c.545G>C	NP_060017.1:p.Gly182Ala
NR_037647.1:n.491G>C
NR_037648.1:n.731G>C
XM_006718879.2:c.35G>C	XP_006718942.1:p.Gly12Ala
XM_006718880.2:c.-2-392G>C	XP_006718943.1:n.-2-392G>C
XM_006718881.2:c.-2-392G>C	XP_006718944.1:n.-2-392G>C
XM_011542895.1:c.35G>C	XP_011541197.1:p.Gly12Ala
XM_011542896.1:c.35G>C	XP_011541198.1:p.Gly12Ala
XM_006718879.3:c.35G>C	XP_006718942.1:p.Gly12Ala
XM_006718881.3:c.-2-392G>C	XP_006718944.1:n.-2-392G>C
XM_011542895.2:c.35G>C	XP_011541197.1:p.Gly12Ala
XM_011542896.2:c.35G>C	XP_011541198.1:p.Gly12Ala
XM_017018000.2:c.545G>C	XP_016873489.1:p.Gly182Ala
XM_017018001.1:c.35G>C	XP_016873490.1:p.Gly12Ala
XM_017018002.1:c.35G>C	XP_016873491.1:p.Gly12Ala
XM_017018003.2:c.-2-392G>C	XP_016873492.1:n.-2-392G>C
XM_017018004.1:c.-2-392G>C	XP_016873493.1:n.-2-392G>C
XM_017018005.1:c.-2-392G>C	XP_016873494.1:n.-2-392G>C
XM_017018006.2:c.-2-392G>C	XP_016873495.1:n.-2-392G>C
NM_017547.4:c.545G>C MANE Select	NP_060017.1:p.Gly182Ala
NR_037647.2:n.377G>C
NR_037648.2:n.722G>C