Canonical Allele Identifier: CA383230272

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145316G>C (hg19) ; chr11:g.126275421G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275421G>C , CM000673.2:g.126275421G>C	GRCh38
NC_000011.9:g.126145316G>C , CM000673.1:g.126145316G>C	GRCh37
NC_000011.8:g.125650526G>C	NCBI36
NG_028029.1:g.11382G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1209G>C
ENST00000532101.6:n.828G>C
ENST00000532125.2:c.723G>C	ENSP00000434178.2:p.Glu241Asp
ENST00000533839.6:c.86-373G>C	ENSP00000509952.1:n.86-373G>C
ENST00000534011.6:n.1018G>C
ENST00000685484.1:c.726G>C	ENSP00000510622.1:p.Glu242Asp
ENST00000685601.1:c.726G>C	ENSP00000510603.1:p.Glu242Asp
ENST00000685765.1:c.726G>C	ENSP00000509991.1:p.Glu242Asp
ENST00000685844.1:c.*263G>C	ENSP00000509820.1:n.*263G>C
ENST00000685857.1:n.1465G>C
ENST00000686242.1:c.525G>C	ENSP00000508950.1:n.525G>C
ENST00000686888.1:c.*293G>C	ENSP00000509619.1:n.*293G>C
ENST00000687699.1:c.850G>C	ENSP00000508878.1:n.850G>C
ENST00000687786.1:n.2162G>C
ENST00000688100.1:n.1647G>C
ENST00000688588.1:c.726G>C	ENSP00000510802.1:p.Glu242Asp
ENST00000688927.1:n.2937G>C
ENST00000689283.1:c.*389G>C	ENSP00000509050.1:n.*389G>C
ENST00000689477.1:c.*619G>C	ENSP00000508945.1:n.*619G>C
ENST00000689765.1:c.*219G>C	ENSP00000509625.1:n.*219G>C
ENST00000690512.1:c.*577G>C	ENSP00000509793.1:n.*577G>C
ENST00000692039.1:c.*524G>C	ENSP00000508821.1:n.*524G>C
ENST00000692336.1:c.750G>C	ENSP00000508540.1:p.Glu250Asp
ENST00000693133.1:n.1206G>C
ENST00000263578.10:c.726G>C MANE Select	ENSP00000263578.5:p.Glu242Asp
ENST00000263578.9:c.726G>C	ENSP00000263578.5:p.Glu242Asp
ENST00000525083.5:n.446G>C
ENST00000525770.5:c.*358G>C	ENSP00000434739.1:n.*358G>C
ENST00000527004.5:c.*70G>C	ENSP00000436374.1:n.*70G>C
ENST00000530642.1:n.1508G>C
ENST00000532101.5:n.949G>C
ENST00000532125.1:c.684G>C	ENSP00000434178.1:p.Glu228Asp
ENST00000533395.5:n.459G>C
ENST00000533839.5:n.238-373G>C
ENST00000534011.5:n.778G>C
ENST00000534315.5:n.1038G>C
NM_017547.3:c.726G>C	NP_060017.1:p.Glu242Asp
NR_037647.1:n.672G>C
NR_037648.1:n.912G>C
XM_006718879.2:c.216G>C	XP_006718942.1:p.Glu72Asp
XM_006718880.2:c.93G>C	XP_006718943.1:p.Glu31Asp
XM_006718881.2:c.93G>C	XP_006718944.1:p.Glu31Asp
XM_011542895.1:c.216G>C	XP_011541197.1:p.Glu72Asp
XM_011542896.1:c.216G>C	XP_011541198.1:p.Glu72Asp
XM_006718879.3:c.216G>C	XP_006718942.1:p.Glu72Asp
XM_006718881.3:c.93G>C	XP_006718944.1:p.Glu31Asp
XM_011542895.2:c.216G>C	XP_011541197.1:p.Glu72Asp
XM_011542896.2:c.216G>C	XP_011541198.1:p.Glu72Asp
XM_017018000.2:c.726G>C	XP_016873489.1:p.Glu242Asp
XM_017018001.1:c.216G>C	XP_016873490.1:p.Glu72Asp
XM_017018002.1:c.216G>C	XP_016873491.1:p.Glu72Asp
XM_017018003.2:c.93G>C	XP_016873492.1:p.Glu31Asp
XM_017018004.1:c.93G>C	XP_016873493.1:p.Glu31Asp
XM_017018005.1:c.93G>C	XP_016873494.1:p.Glu31Asp
XM_017018006.2:c.93G>C	XP_016873495.1:p.Glu31Asp
NM_017547.4:c.726G>C MANE Select	NP_060017.1:p.Glu242Asp
NR_037647.2:n.558G>C
NR_037648.2:n.903G>C