Canonical Allele Identifier: CA383230005

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126144892G>C (hg19) ; chr11:g.126274997G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274997G>C , CM000673.2:g.126274997G>C	GRCh38
NC_000011.9:g.126144892G>C , CM000673.1:g.126144892G>C	GRCh37
NC_000011.8:g.125650102G>C	NCBI36
NG_028029.1:g.10958G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.785G>C
ENST00000532101.6:n.734-330G>C
ENST00000532125.2:c.604G>C	ENSP00000434178.2:p.Glu202Gln
ENST00000533839.6:c.86-797G>C	ENSP00000509952.1:n.86-797G>C
ENST00000534011.6:n.899G>C
ENST00000685484.1:c.607G>C	ENSP00000510622.1:p.Glu203Gln
ENST00000685601.1:c.607G>C	ENSP00000510603.1:p.Glu203Gln
ENST00000685765.1:c.607G>C	ENSP00000509991.1:p.Glu203Gln
ENST00000685844.1:c.*169-330G>C	ENSP00000509820.1:n.*169-330G>C
ENST00000685857.1:n.1041G>C
ENST00000686242.1:c.406G>C	ENSP00000508950.1:n.406G>C
ENST00000686888.1:c.*174G>C	ENSP00000509619.1:n.*174G>C
ENST00000687699.1:c.731G>C	ENSP00000508878.1:n.731G>C
ENST00000687786.1:n.2068-330G>C
ENST00000688100.1:n.1528G>C
ENST00000688588.1:c.607G>C	ENSP00000510802.1:p.Glu203Gln
ENST00000688927.1:n.2513G>C
ENST00000689283.1:c.*270G>C	ENSP00000509050.1:n.*270G>C
ENST00000689477.1:c.*500G>C	ENSP00000508945.1:n.*500G>C
ENST00000689765.1:c.*169-374G>C	ENSP00000509625.1:n.*169-374G>C
ENST00000690512.1:c.*458G>C	ENSP00000509793.1:n.*458G>C
ENST00000692039.1:c.*405G>C	ENSP00000508821.1:n.*405G>C
ENST00000692336.1:c.631G>C	ENSP00000508540.1:p.Glu211Gln
ENST00000693133.1:n.782G>C
ENST00000263578.10:c.607G>C MANE Select	ENSP00000263578.5:p.Glu203Gln
ENST00000263578.9:c.607G>C	ENSP00000263578.5:p.Glu203Gln
ENST00000524751.5:n.543G>C
ENST00000525083.5:n.352-330G>C
ENST00000525770.5:c.*239G>C	ENSP00000434739.1:n.*239G>C
ENST00000526366.5:n.538G>C
ENST00000527004.5:c.534-330G>C	ENSP00000436374.1:n.534-330G>C
ENST00000527875.1:n.437G>C
ENST00000530642.1:n.1084G>C
ENST00000532101.5:n.830G>C
ENST00000532125.1:c.565G>C	ENSP00000434178.1:p.Glu189Gln
ENST00000533395.5:n.365-330G>C
ENST00000533839.5:n.238-797G>C
ENST00000534011.5:n.659G>C
ENST00000534315.5:n.944-330G>C
NM_017547.3:c.607G>C	NP_060017.1:p.Glu203Gln
NR_037647.1:n.553G>C
NR_037648.1:n.793G>C
XM_006718879.2:c.97G>C	XP_006718942.1:p.Glu33Gln
XM_006718880.2:c.-2-330G>C	XP_006718943.1:n.-2-330G>C
XM_006718881.2:c.-2-330G>C	XP_006718944.1:n.-2-330G>C
XM_011542895.1:c.97G>C	XP_011541197.1:p.Glu33Gln
XM_011542896.1:c.97G>C	XP_011541198.1:p.Glu33Gln
XM_006718879.3:c.97G>C	XP_006718942.1:p.Glu33Gln
XM_006718881.3:c.-2-330G>C	XP_006718944.1:n.-2-330G>C
XM_011542895.2:c.97G>C	XP_011541197.1:p.Glu33Gln
XM_011542896.2:c.97G>C	XP_011541198.1:p.Glu33Gln
XM_017018000.2:c.607G>C	XP_016873489.1:p.Glu203Gln
XM_017018001.1:c.97G>C	XP_016873490.1:p.Glu33Gln
XM_017018002.1:c.97G>C	XP_016873491.1:p.Glu33Gln
XM_017018003.2:c.-2-330G>C	XP_016873492.1:n.-2-330G>C
XM_017018004.1:c.-2-330G>C	XP_016873493.1:n.-2-330G>C
XM_017018005.1:c.-2-330G>C	XP_016873494.1:n.-2-330G>C
XM_017018006.2:c.-2-330G>C	XP_016873495.1:n.-2-330G>C
NM_017547.4:c.607G>C MANE Select	NP_060017.1:p.Glu203Gln
NR_037647.2:n.439G>C
NR_037648.2:n.784G>C