Canonical Allele Identifier: CA383230270

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145315A>G (hg19) ; chr11:g.126275420A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275420A>G , CM000673.2:g.126275420A>G	GRCh38
NC_000011.9:g.126145315A>G , CM000673.1:g.126145315A>G	GRCh37
NC_000011.8:g.125650525A>G	NCBI36
NG_028029.1:g.11381A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1208A>G
ENST00000532101.6:n.827A>G
ENST00000532125.2:c.722A>G	ENSP00000434178.2:p.Glu241Gly
ENST00000533839.6:c.86-374A>G	ENSP00000509952.1:n.86-374A>G
ENST00000534011.6:n.1017A>G
ENST00000685484.1:c.725A>G	ENSP00000510622.1:p.Glu242Gly
ENST00000685601.1:c.725A>G	ENSP00000510603.1:p.Glu242Gly
ENST00000685765.1:c.725A>G	ENSP00000509991.1:p.Glu242Gly
ENST00000685844.1:c.*262A>G	ENSP00000509820.1:n.*262A>G
ENST00000685857.1:n.1464A>G
ENST00000686242.1:c.524A>G	ENSP00000508950.1:n.524A>G
ENST00000686888.1:c.*292A>G	ENSP00000509619.1:n.*292A>G
ENST00000687699.1:c.849A>G	ENSP00000508878.1:n.849A>G
ENST00000687786.1:n.2161A>G
ENST00000688100.1:n.1646A>G
ENST00000688588.1:c.725A>G	ENSP00000510802.1:p.Glu242Gly
ENST00000688927.1:n.2936A>G
ENST00000689283.1:c.*388A>G	ENSP00000509050.1:n.*388A>G
ENST00000689477.1:c.*618A>G	ENSP00000508945.1:n.*618A>G
ENST00000689765.1:c.*218A>G	ENSP00000509625.1:n.*218A>G
ENST00000690512.1:c.*576A>G	ENSP00000509793.1:n.*576A>G
ENST00000692039.1:c.*523A>G	ENSP00000508821.1:n.*523A>G
ENST00000692336.1:c.749A>G	ENSP00000508540.1:p.Glu250Gly
ENST00000693133.1:n.1205A>G
ENST00000263578.10:c.725A>G MANE Select	ENSP00000263578.5:p.Glu242Gly
ENST00000263578.9:c.725A>G	ENSP00000263578.5:p.Glu242Gly
ENST00000525083.5:n.445A>G
ENST00000525770.5:c.*357A>G	ENSP00000434739.1:n.*357A>G
ENST00000527004.5:c.*69A>G	ENSP00000436374.1:n.*69A>G
ENST00000530642.1:n.1507A>G
ENST00000532101.5:n.948A>G
ENST00000532125.1:c.683A>G	ENSP00000434178.1:p.Glu228Gly
ENST00000533395.5:n.458A>G
ENST00000533839.5:n.238-374A>G
ENST00000534011.5:n.777A>G
ENST00000534315.5:n.1037A>G
NM_017547.3:c.725A>G	NP_060017.1:p.Glu242Gly
NR_037647.1:n.671A>G
NR_037648.1:n.911A>G
XM_006718879.2:c.215A>G	XP_006718942.1:p.Glu72Gly
XM_006718880.2:c.92A>G	XP_006718943.1:p.Glu31Gly
XM_006718881.2:c.92A>G	XP_006718944.1:p.Glu31Gly
XM_011542895.1:c.215A>G	XP_011541197.1:p.Glu72Gly
XM_011542896.1:c.215A>G	XP_011541198.1:p.Glu72Gly
XM_006718879.3:c.215A>G	XP_006718942.1:p.Glu72Gly
XM_006718881.3:c.92A>G	XP_006718944.1:p.Glu31Gly
XM_011542895.2:c.215A>G	XP_011541197.1:p.Glu72Gly
XM_011542896.2:c.215A>G	XP_011541198.1:p.Glu72Gly
XM_017018000.2:c.725A>G	XP_016873489.1:p.Glu242Gly
XM_017018001.1:c.215A>G	XP_016873490.1:p.Glu72Gly
XM_017018002.1:c.215A>G	XP_016873491.1:p.Glu72Gly
XM_017018003.2:c.92A>G	XP_016873492.1:p.Glu31Gly
XM_017018004.1:c.92A>G	XP_016873493.1:p.Glu31Gly
XM_017018005.1:c.92A>G	XP_016873494.1:p.Glu31Gly
XM_017018006.2:c.92A>G	XP_016873495.1:p.Glu31Gly
NM_017547.4:c.725A>G MANE Select	NP_060017.1:p.Glu242Gly
NR_037647.2:n.557A>G
NR_037648.2:n.902A>G