Canonical Allele Identifier: CA383230267

Gene: FOXRED1

Linked Data

• gnomAD v4: 11-126275419-G-C
• MyVariant Identifiers: chr11:g.126145314G>C (hg19) ; chr11:g.126275419G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275419G>C , CM000673.2:g.126275419G>C	GRCh38
NC_000011.9:g.126145314G>C , CM000673.1:g.126145314G>C	GRCh37
NC_000011.8:g.125650524G>C	NCBI36
NG_028029.1:g.11380G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1207G>C
ENST00000532101.6:n.826G>C
ENST00000532125.2:c.721G>C	ENSP00000434178.2:p.Glu241Gln
ENST00000533839.6:c.86-375G>C	ENSP00000509952.1:n.86-375G>C
ENST00000534011.6:n.1016G>C
ENST00000685484.1:c.724G>C	ENSP00000510622.1:p.Glu242Gln
ENST00000685601.1:c.724G>C	ENSP00000510603.1:p.Glu242Gln
ENST00000685765.1:c.724G>C	ENSP00000509991.1:p.Glu242Gln
ENST00000685844.1:c.*261G>C	ENSP00000509820.1:n.*261G>C
ENST00000685857.1:n.1463G>C
ENST00000686242.1:c.523G>C	ENSP00000508950.1:n.523G>C
ENST00000686888.1:c.*291G>C	ENSP00000509619.1:n.*291G>C
ENST00000687699.1:c.848G>C	ENSP00000508878.1:n.848G>C
ENST00000687786.1:n.2160G>C
ENST00000688100.1:n.1645G>C
ENST00000688588.1:c.724G>C	ENSP00000510802.1:p.Glu242Gln
ENST00000688927.1:n.2935G>C
ENST00000689283.1:c.*387G>C	ENSP00000509050.1:n.*387G>C
ENST00000689477.1:c.*617G>C	ENSP00000508945.1:n.*617G>C
ENST00000689765.1:c.*217G>C	ENSP00000509625.1:n.*217G>C
ENST00000690512.1:c.*575G>C	ENSP00000509793.1:n.*575G>C
ENST00000692039.1:c.*522G>C	ENSP00000508821.1:n.*522G>C
ENST00000692336.1:c.748G>C	ENSP00000508540.1:p.Glu250Gln
ENST00000693133.1:n.1204G>C
ENST00000263578.10:c.724G>C MANE Select	ENSP00000263578.5:p.Glu242Gln
ENST00000263578.9:c.724G>C	ENSP00000263578.5:p.Glu242Gln
ENST00000525083.5:n.444G>C
ENST00000525770.5:c.*356G>C	ENSP00000434739.1:n.*356G>C
ENST00000527004.5:c.*68G>C	ENSP00000436374.1:n.*68G>C
ENST00000530642.1:n.1506G>C
ENST00000532101.5:n.947G>C
ENST00000532125.1:c.682G>C	ENSP00000434178.1:p.Glu228Gln
ENST00000533395.5:n.457G>C
ENST00000533839.5:n.238-375G>C
ENST00000534011.5:n.776G>C
ENST00000534315.5:n.1036G>C
NM_017547.3:c.724G>C	NP_060017.1:p.Glu242Gln
NR_037647.1:n.670G>C
NR_037648.1:n.910G>C
XM_006718879.2:c.214G>C	XP_006718942.1:p.Glu72Gln
XM_006718880.2:c.91G>C	XP_006718943.1:p.Glu31Gln
XM_006718881.2:c.91G>C	XP_006718944.1:p.Glu31Gln
XM_011542895.1:c.214G>C	XP_011541197.1:p.Glu72Gln
XM_011542896.1:c.214G>C	XP_011541198.1:p.Glu72Gln
XM_006718879.3:c.214G>C	XP_006718942.1:p.Glu72Gln
XM_006718881.3:c.91G>C	XP_006718944.1:p.Glu31Gln
XM_011542895.2:c.214G>C	XP_011541197.1:p.Glu72Gln
XM_011542896.2:c.214G>C	XP_011541198.1:p.Glu72Gln
XM_017018000.2:c.724G>C	XP_016873489.1:p.Glu242Gln
XM_017018001.1:c.214G>C	XP_016873490.1:p.Glu72Gln
XM_017018002.1:c.214G>C	XP_016873491.1:p.Glu72Gln
XM_017018003.2:c.91G>C	XP_016873492.1:p.Glu31Gln
XM_017018004.1:c.91G>C	XP_016873493.1:p.Glu31Gln
XM_017018005.1:c.91G>C	XP_016873494.1:p.Glu31Gln
XM_017018006.2:c.91G>C	XP_016873495.1:p.Glu31Gln
NM_017547.4:c.724G>C MANE Select	NP_060017.1:p.Glu242Gln
NR_037647.2:n.556G>C
NR_037648.2:n.901G>C