Canonical Allele Identifier: CA383230172

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145266G>C (hg19) ; chr11:g.126275371G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275371G>C , CM000673.2:g.126275371G>C	GRCh38
NC_000011.9:g.126145266G>C , CM000673.1:g.126145266G>C	GRCh37
NC_000011.8:g.125650476G>C	NCBI36
NG_028029.1:g.11332G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1159G>C
ENST00000532101.6:n.778G>C
ENST00000532125.2:c.673G>C	ENSP00000434178.2:p.Gly225Arg
ENST00000533839.6:c.86-423G>C	ENSP00000509952.1:n.86-423G>C
ENST00000534011.6:n.968G>C
ENST00000685484.1:c.676G>C	ENSP00000510622.1:p.Gly226Arg
ENST00000685601.1:c.676G>C	ENSP00000510603.1:p.Gly226Arg
ENST00000685765.1:c.676G>C	ENSP00000509991.1:p.Gly226Arg
ENST00000685844.1:c.*213G>C	ENSP00000509820.1:n.*213G>C
ENST00000685857.1:n.1415G>C
ENST00000686242.1:c.475G>C	ENSP00000508950.1:n.475G>C
ENST00000686888.1:c.*243G>C	ENSP00000509619.1:n.*243G>C
ENST00000687699.1:c.800G>C	ENSP00000508878.1:n.800G>C
ENST00000687786.1:n.2112G>C
ENST00000688100.1:n.1597G>C
ENST00000688588.1:c.676G>C	ENSP00000510802.1:p.Gly226Arg
ENST00000688927.1:n.2887G>C
ENST00000689283.1:c.*339G>C	ENSP00000509050.1:n.*339G>C
ENST00000689477.1:c.*569G>C	ENSP00000508945.1:n.*569G>C
ENST00000689765.1:c.*169G>C	ENSP00000509625.1:n.*169G>C
ENST00000690512.1:c.*527G>C	ENSP00000509793.1:n.*527G>C
ENST00000692039.1:c.*474G>C	ENSP00000508821.1:n.*474G>C
ENST00000692336.1:c.700G>C	ENSP00000508540.1:p.Gly234Arg
ENST00000693133.1:n.1156G>C
ENST00000263578.10:c.676G>C MANE Select	ENSP00000263578.5:p.Gly226Arg
ENST00000263578.9:c.676G>C	ENSP00000263578.5:p.Gly226Arg
ENST00000525083.5:n.396G>C
ENST00000525770.5:c.*308G>C	ENSP00000434739.1:n.*308G>C
ENST00000527004.5:c.*20G>C	ENSP00000436374.1:n.*20G>C
ENST00000530642.1:n.1458G>C
ENST00000532101.5:n.899G>C
ENST00000532125.1:c.634G>C	ENSP00000434178.1:p.Gly212Arg
ENST00000533395.5:n.409G>C
ENST00000533839.5:n.238-423G>C
ENST00000534011.5:n.728G>C
ENST00000534315.5:n.988G>C
NM_017547.3:c.676G>C	NP_060017.1:p.Gly226Arg
NR_037647.1:n.622G>C
NR_037648.1:n.862G>C
XM_006718879.2:c.166G>C	XP_006718942.1:p.Gly56Arg
XM_006718880.2:c.43G>C	XP_006718943.1:p.Gly15Arg
XM_006718881.2:c.43G>C	XP_006718944.1:p.Gly15Arg
XM_011542895.1:c.166G>C	XP_011541197.1:p.Gly56Arg
XM_011542896.1:c.166G>C	XP_011541198.1:p.Gly56Arg
XM_006718879.3:c.166G>C	XP_006718942.1:p.Gly56Arg
XM_006718881.3:c.43G>C	XP_006718944.1:p.Gly15Arg
XM_011542895.2:c.166G>C	XP_011541197.1:p.Gly56Arg
XM_011542896.2:c.166G>C	XP_011541198.1:p.Gly56Arg
XM_017018000.2:c.676G>C	XP_016873489.1:p.Gly226Arg
XM_017018001.1:c.166G>C	XP_016873490.1:p.Gly56Arg
XM_017018002.1:c.166G>C	XP_016873491.1:p.Gly56Arg
XM_017018003.2:c.43G>C	XP_016873492.1:p.Gly15Arg
XM_017018004.1:c.43G>C	XP_016873493.1:p.Gly15Arg
XM_017018005.1:c.43G>C	XP_016873494.1:p.Gly15Arg
XM_017018006.2:c.43G>C	XP_016873495.1:p.Gly15Arg
NM_017547.4:c.676G>C MANE Select	NP_060017.1:p.Gly226Arg
NR_037647.2:n.508G>C
NR_037648.2:n.853G>C