Canonical Allele Identifier: CA383230184

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145273G>T (hg19) ; chr11:g.126275378G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275378G>T , CM000673.2:g.126275378G>T	GRCh38
NC_000011.9:g.126145273G>T , CM000673.1:g.126145273G>T	GRCh37
NC_000011.8:g.125650483G>T	NCBI36
NG_028029.1:g.11339G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1166G>T
ENST00000532101.6:n.785G>T
ENST00000532125.2:c.680G>T	ENSP00000434178.2:p.Arg227Leu
ENST00000533839.6:c.86-416G>T	ENSP00000509952.1:n.86-416G>T
ENST00000534011.6:n.975G>T
ENST00000685484.1:c.683G>T	ENSP00000510622.1:p.Arg228Leu
ENST00000685601.1:c.683G>T	ENSP00000510603.1:p.Arg228Leu
ENST00000685765.1:c.683G>T	ENSP00000509991.1:p.Arg228Leu
ENST00000685844.1:c.*220G>T	ENSP00000509820.1:n.*220G>T
ENST00000685857.1:n.1422G>T
ENST00000686242.1:c.482G>T	ENSP00000508950.1:n.482G>T
ENST00000686888.1:c.*250G>T	ENSP00000509619.1:n.*250G>T
ENST00000687699.1:c.807G>T	ENSP00000508878.1:n.807G>T
ENST00000687786.1:n.2119G>T
ENST00000688100.1:n.1604G>T
ENST00000688588.1:c.683G>T	ENSP00000510802.1:p.Arg228Leu
ENST00000688927.1:n.2894G>T
ENST00000689283.1:c.*346G>T	ENSP00000509050.1:n.*346G>T
ENST00000689477.1:c.*576G>T	ENSP00000508945.1:n.*576G>T
ENST00000689765.1:c.*176G>T	ENSP00000509625.1:n.*176G>T
ENST00000690512.1:c.*534G>T	ENSP00000509793.1:n.*534G>T
ENST00000692039.1:c.*481G>T	ENSP00000508821.1:n.*481G>T
ENST00000692336.1:c.707G>T	ENSP00000508540.1:p.Arg236Leu
ENST00000693133.1:n.1163G>T
ENST00000263578.10:c.683G>T MANE Select	ENSP00000263578.5:p.Arg228Leu
ENST00000263578.9:c.683G>T	ENSP00000263578.5:p.Arg228Leu
ENST00000525083.5:n.403G>T
ENST00000525770.5:c.*315G>T	ENSP00000434739.1:n.*315G>T
ENST00000527004.5:c.*27G>T	ENSP00000436374.1:n.*27G>T
ENST00000530642.1:n.1465G>T
ENST00000532101.5:n.906G>T
ENST00000532125.1:c.641G>T	ENSP00000434178.1:p.Arg214Leu
ENST00000533395.5:n.416G>T
ENST00000533839.5:n.238-416G>T
ENST00000534011.5:n.735G>T
ENST00000534315.5:n.995G>T
NM_017547.3:c.683G>T	NP_060017.1:p.Arg228Leu
NR_037647.1:n.629G>T
NR_037648.1:n.869G>T
XM_006718879.2:c.173G>T	XP_006718942.1:p.Arg58Leu
XM_006718880.2:c.50G>T	XP_006718943.1:p.Arg17Leu
XM_006718881.2:c.50G>T	XP_006718944.1:p.Arg17Leu
XM_011542895.1:c.173G>T	XP_011541197.1:p.Arg58Leu
XM_011542896.1:c.173G>T	XP_011541198.1:p.Arg58Leu
XM_006718879.3:c.173G>T	XP_006718942.1:p.Arg58Leu
XM_006718881.3:c.50G>T	XP_006718944.1:p.Arg17Leu
XM_011542895.2:c.173G>T	XP_011541197.1:p.Arg58Leu
XM_011542896.2:c.173G>T	XP_011541198.1:p.Arg58Leu
XM_017018000.2:c.683G>T	XP_016873489.1:p.Arg228Leu
XM_017018001.1:c.173G>T	XP_016873490.1:p.Arg58Leu
XM_017018002.1:c.173G>T	XP_016873491.1:p.Arg58Leu
XM_017018003.2:c.50G>T	XP_016873492.1:p.Arg17Leu
XM_017018004.1:c.50G>T	XP_016873493.1:p.Arg17Leu
XM_017018005.1:c.50G>T	XP_016873494.1:p.Arg17Leu
XM_017018006.2:c.50G>T	XP_016873495.1:p.Arg17Leu
NM_017547.4:c.683G>T MANE Select	NP_060017.1:p.Arg228Leu
NR_037647.2:n.515G>T
NR_037648.2:n.860G>T