Canonical Allele Identifier: CA383230100

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145234A>T (hg19) ; chr11:g.126275339A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275339A>T , CM000673.2:g.126275339A>T	GRCh38
NC_000011.9:g.126145234A>T , CM000673.1:g.126145234A>T	GRCh37
NC_000011.8:g.125650444A>T	NCBI36
NG_028029.1:g.11300A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1127A>T
ENST00000532101.6:n.746A>T
ENST00000532125.2:c.641A>T	ENSP00000434178.2:p.Glu214Val
ENST00000533839.6:c.86-455A>T	ENSP00000509952.1:n.86-455A>T
ENST00000534011.6:n.936A>T
ENST00000685484.1:c.644A>T	ENSP00000510622.1:p.Glu215Val
ENST00000685601.1:c.644A>T	ENSP00000510603.1:p.Glu215Val
ENST00000685765.1:c.644A>T	ENSP00000509991.1:p.Glu215Val
ENST00000685844.1:c.*181A>T	ENSP00000509820.1:n.*181A>T
ENST00000685857.1:n.1383A>T
ENST00000686242.1:c.443A>T	ENSP00000508950.1:n.443A>T
ENST00000686888.1:c.*211A>T	ENSP00000509619.1:n.*211A>T
ENST00000687699.1:c.768A>T	ENSP00000508878.1:n.768A>T
ENST00000687786.1:n.2080A>T
ENST00000688100.1:n.1565A>T
ENST00000688588.1:c.644A>T	ENSP00000510802.1:p.Glu215Val
ENST00000688927.1:n.2855A>T
ENST00000689283.1:c.*307A>T	ENSP00000509050.1:n.*307A>T
ENST00000689477.1:c.*537A>T	ENSP00000508945.1:n.*537A>T
ENST00000689765.1:c.*169-32A>T	ENSP00000509625.1:n.*169-32A>T
ENST00000690512.1:c.*495A>T	ENSP00000509793.1:n.*495A>T
ENST00000692039.1:c.*442A>T	ENSP00000508821.1:n.*442A>T
ENST00000692336.1:c.668A>T	ENSP00000508540.1:p.Glu223Val
ENST00000693133.1:n.1124A>T
ENST00000263578.10:c.644A>T MANE Select	ENSP00000263578.5:p.Glu215Val
ENST00000263578.9:c.644A>T	ENSP00000263578.5:p.Glu215Val
ENST00000524751.5:n.885A>T
ENST00000525083.5:n.364A>T
ENST00000525770.5:c.*276A>T	ENSP00000434739.1:n.*276A>T
ENST00000527004.5:c.546A>T	ENSP00000436374.1:p.Arg182=
ENST00000530642.1:n.1426A>T
ENST00000532101.5:n.867A>T
ENST00000532125.1:c.602A>T	ENSP00000434178.1:p.Glu201Val
ENST00000533395.5:n.377A>T
ENST00000533839.5:n.238-455A>T
ENST00000534011.5:n.696A>T
ENST00000534315.5:n.956A>T
NM_017547.3:c.644A>T	NP_060017.1:p.Glu215Val
NR_037647.1:n.590A>T
NR_037648.1:n.830A>T
XM_006718879.2:c.134A>T	XP_006718942.1:p.Glu45Val
XM_006718880.2:c.11A>T	XP_006718943.1:p.Glu4Val
XM_006718881.2:c.11A>T	XP_006718944.1:p.Glu4Val
XM_011542895.1:c.134A>T	XP_011541197.1:p.Glu45Val
XM_011542896.1:c.134A>T	XP_011541198.1:p.Glu45Val
XM_006718879.3:c.134A>T	XP_006718942.1:p.Glu45Val
XM_006718881.3:c.11A>T	XP_006718944.1:p.Glu4Val
XM_011542895.2:c.134A>T	XP_011541197.1:p.Glu45Val
XM_011542896.2:c.134A>T	XP_011541198.1:p.Glu45Val
XM_017018000.2:c.644A>T	XP_016873489.1:p.Glu215Val
XM_017018001.1:c.134A>T	XP_016873490.1:p.Glu45Val
XM_017018002.1:c.134A>T	XP_016873491.1:p.Glu45Val
XM_017018003.2:c.11A>T	XP_016873492.1:p.Glu4Val
XM_017018004.1:c.11A>T	XP_016873493.1:p.Glu4Val
XM_017018005.1:c.11A>T	XP_016873494.1:p.Glu4Val
XM_017018006.2:c.11A>T	XP_016873495.1:p.Glu4Val
NM_017547.4:c.644A>T MANE Select	NP_060017.1:p.Glu215Val
NR_037647.2:n.476A>T
NR_037648.2:n.821A>T