Canonical Allele Identifier: CA2007079547

Gene: FOXRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274984_126274985delinsCT , CM000673.2:g.126274984_126274985delinsCT	GRCh38
NC_000011.9:g.126144879_126144880delinsCT , CM000673.1:g.126144879_126144880delinsCT	GRCh37
NC_000011.8:g.125650089_125650090delinsCT	NCBI36
NG_028029.1:g.10945_10946delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.772_773delinsCT
ENST00000532101.6:n.734-343_734-342delinsCT
ENST00000532125.2:c.591_592delinsCT	ENSP00000434178.2:p.Pro197=
ENST00000533839.6:c.86-810_86-809delinsCT	ENSP00000509952.1:n.86-810_86-809delinsCT
ENST00000534011.6:n.886_887delinsCT
ENST00000685484.1:c.594_595delinsCT	ENSP00000510622.1:p.Pro198=
ENST00000685601.1:c.594_595delinsCT	ENSP00000510603.1:p.Pro198=
ENST00000685765.1:c.594_595delinsCT	ENSP00000509991.1:p.Pro198=
ENST00000685844.1:c.*169-343_*169-342delinsCT	ENSP00000509820.1:n.*169-343_*169-342delinsCT
ENST00000685857.1:n.1028_1029delinsCT
ENST00000686242.1:c.393_394delinsCT	ENSP00000508950.1:n.393_394delinsCT
ENST00000686888.1:c.*161_*162delinsCT	ENSP00000509619.1:n.*161_*162delinsCT
ENST00000687699.1:c.718_719delinsCT	ENSP00000508878.1:n.718_719delinsCT
ENST00000687786.1:n.2068-343_2068-342delinsCT
ENST00000688100.1:n.1515_1516delinsCT
ENST00000688588.1:c.594_595delinsCT	ENSP00000510802.1:p.Pro198=
ENST00000688927.1:n.2500_2501delinsCT
ENST00000689283.1:c.*257_*258delinsCT	ENSP00000509050.1:n.*257_*258delinsCT
ENST00000689477.1:c.*487_*488delinsCT	ENSP00000508945.1:n.*487_*488delinsCT
ENST00000689765.1:c.*169-387_*169-386delinsCT	ENSP00000509625.1:n.*169-387_*169-386delinsCT
ENST00000690512.1:c.*445_*446delinsCT	ENSP00000509793.1:n.*445_*446delinsCT
ENST00000692039.1:c.*392_*393delinsCT	ENSP00000508821.1:n.*392_*393delinsCT
ENST00000692336.1:c.618_619delinsCT	ENSP00000508540.1:p.Pro206=
ENST00000693133.1:n.769_770delinsCT
ENST00000263578.10:c.594_595delinsCT MANE Select	ENSP00000263578.5:p.Pro198=
ENST00000263578.9:c.594_595delinsCT	ENSP00000263578.5:p.Pro198=
ENST00000524751.5:n.530_531delinsCT
ENST00000525083.5:n.352-343_352-342delinsCT
ENST00000525770.5:c.*226_*227delinsCT	ENSP00000434739.1:n.*226_*227delinsCT
ENST00000526366.5:n.525_526delinsCT
ENST00000527004.5:c.534-343_534-342delinsCT	ENSP00000436374.1:n.534-343_534-342delinsCT
ENST00000527875.1:n.424_425delinsCT
ENST00000530642.1:n.1071_1072delinsCT
ENST00000532101.5:n.817_818delinsCT
ENST00000532125.1:c.552_553delinsCT	ENSP00000434178.1:p.Pro184=
ENST00000533395.5:n.365-343_365-342delinsCT
ENST00000533839.5:n.238-810_238-809delinsCT
ENST00000534011.5:n.646_647delinsCT
ENST00000534315.5:n.944-343_944-342delinsCT
NM_017547.3:c.594_595delinsCT	NP_060017.1:p.Pro198=
NR_037647.1:n.540_541delinsCT
NR_037648.1:n.780_781delinsCT
XM_006718879.2:c.84_85delinsCT	XP_006718942.1:p.Pro28=
XM_006718880.2:c.-2-343_-2-342delinsCT	XP_006718943.1:n.-2-343_-2-342delinsCT
XM_006718881.2:c.-2-343_-2-342delinsCT	XP_006718944.1:n.-2-343_-2-342delinsCT
XM_011542895.1:c.84_85delinsCT	XP_011541197.1:p.Pro28=
XM_011542896.1:c.84_85delinsCT	XP_011541198.1:p.Pro28=
XM_006718879.3:c.84_85delinsCT	XP_006718942.1:p.Pro28=
XM_006718881.3:c.-2-343_-2-342delinsCT	XP_006718944.1:n.-2-343_-2-342delinsCT
XM_011542895.2:c.84_85delinsCT	XP_011541197.1:p.Pro28=
XM_011542896.2:c.84_85delinsCT	XP_011541198.1:p.Pro28=
XM_017018000.2:c.594_595delinsCT	XP_016873489.1:p.Pro198=
XM_017018001.1:c.84_85delinsCT	XP_016873490.1:p.Pro28=
XM_017018002.1:c.84_85delinsCT	XP_016873491.1:p.Pro28=
XM_017018003.2:c.-2-343_-2-342delinsCT	XP_016873492.1:n.-2-343_-2-342delinsCT
XM_017018004.1:c.-2-343_-2-342delinsCT	XP_016873493.1:n.-2-343_-2-342delinsCT
XM_017018005.1:c.-2-343_-2-342delinsCT	XP_016873494.1:n.-2-343_-2-342delinsCT
XM_017018006.2:c.-2-343_-2-342delinsCT	XP_016873495.1:n.-2-343_-2-342delinsCT
NM_017547.4:c.594_595delinsCT MANE Select	NP_060017.1:p.Pro198=
NR_037647.2:n.426_427delinsCT
NR_037648.2:n.771_772delinsCT