Canonical Allele Identifier: CA2007079556

Gene: FOXRED1

Linked Data

• dbSNP Id: rs1951091106
• gnomAD v4: 11-126274995-CAGAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274996_126274999del , CM000673.2:g.126274996_126274999del	GRCh38
NC_000011.9:g.126144891_126144894del , CM000673.1:g.126144891_126144894del	GRCh37
NC_000011.8:g.125650101_125650104del	NCBI36
NG_028029.1:g.10957_10960del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.784_787del
ENST00000532101.6:n.734-331_734-328del
ENST00000532125.2:c.603_606del	ENSP00000434178.2:p.Gly203TrpfsTer?
ENST00000533839.6:c.86-798_86-795del	ENSP00000509952.1:n.86-798_86-795del
ENST00000534011.6:n.898_901del
ENST00000685484.1:c.606_609del	ENSP00000510622.1:p.Gly204TrpfsTer?
ENST00000685601.1:c.606_609del	ENSP00000510603.1:p.Gly204TrpfsTer?
ENST00000685765.1:c.606_609del	ENSP00000509991.1:p.Gly204TrpfsTer?
ENST00000685844.1:c.*169-331_*169-328del	ENSP00000509820.1:n.*169-331_*169-328del
ENST00000685857.1:n.1040_1043del
ENST00000686242.1:c.405_408del	ENSP00000508950.1:n.405_408del
ENST00000686888.1:c.*173_*176del	ENSP00000509619.1:n.*173_*176del
ENST00000687699.1:c.730_733del	ENSP00000508878.1:n.730_733del
ENST00000687786.1:n.2068-331_2068-328del
ENST00000688100.1:n.1527_1530del
ENST00000688588.1:c.606_609del	ENSP00000510802.1:p.Gly204TrpfsTer?
ENST00000688927.1:n.2512_2515del
ENST00000689283.1:c.*269_*272del	ENSP00000509050.1:n.*269_*272del
ENST00000689477.1:c.*499_*502del	ENSP00000508945.1:n.*499_*502del
ENST00000689765.1:c.*169-375_*169-372del	ENSP00000509625.1:n.*169-375_*169-372del
ENST00000690512.1:c.*457_*460del	ENSP00000509793.1:n.*457_*460del
ENST00000692039.1:c.*404_*407del	ENSP00000508821.1:n.*404_*407del
ENST00000692336.1:c.630_633del	ENSP00000508540.1:p.Gly212TrpfsTer?
ENST00000693133.1:n.781_784del
ENST00000263578.10:c.606_609del MANE Select	ENSP00000263578.5:p.Gly204TrpfsTer?
ENST00000263578.9:c.606_609del	ENSP00000263578.5:p.Gly204TrpfsTer?
ENST00000524751.5:n.542_545del
ENST00000525083.5:n.352-331_352-328del
ENST00000525770.5:c.*238_*241del	ENSP00000434739.1:n.*238_*241del
ENST00000526366.5:n.537_540del
ENST00000527004.5:c.534-331_534-328del	ENSP00000436374.1:n.534-331_534-328del
ENST00000527875.1:n.436_439del
ENST00000530642.1:n.1083_1086del
ENST00000532101.5:n.829_832del
ENST00000532125.1:c.564_567del	ENSP00000434178.1:p.Gly190TrpfsTer?
ENST00000533395.5:n.365-331_365-328del
ENST00000533839.5:n.238-798_238-795del
ENST00000534011.5:n.658_661del
ENST00000534315.5:n.944-331_944-328del
NM_017547.3:c.606_609del	NP_060017.1:p.Gly204TrpfsTer?
NR_037647.1:n.552_555del
NR_037648.1:n.792_795del
XM_006718879.2:c.96_99del	XP_006718942.1:p.Gly34TrpfsTer?
XM_006718880.2:c.-2-331_-2-328del	XP_006718943.1:n.-2-331_-2-328del
XM_006718881.2:c.-2-331_-2-328del	XP_006718944.1:n.-2-331_-2-328del
XM_011542895.1:c.96_99del	XP_011541197.1:p.Gly34TrpfsTer?
XM_011542896.1:c.96_99del	XP_011541198.1:p.Gly34TrpfsTer?
XM_006718879.3:c.96_99del	XP_006718942.1:p.Gly34TrpfsTer?
XM_006718881.3:c.-2-331_-2-328del	XP_006718944.1:n.-2-331_-2-328del
XM_011542895.2:c.96_99del	XP_011541197.1:p.Gly34TrpfsTer?
XM_011542896.2:c.96_99del	XP_011541198.1:p.Gly34TrpfsTer?
XM_017018000.2:c.606_609del	XP_016873489.1:p.Gly204TrpfsTer?
XM_017018001.1:c.96_99del	XP_016873490.1:p.Gly34TrpfsTer?
XM_017018002.1:c.96_99del	XP_016873491.1:p.Gly34TrpfsTer?
XM_017018003.2:c.-2-331_-2-328del	XP_016873492.1:n.-2-331_-2-328del
XM_017018004.1:c.-2-331_-2-328del	XP_016873493.1:n.-2-331_-2-328del
XM_017018005.1:c.-2-331_-2-328del	XP_016873494.1:n.-2-331_-2-328del
XM_017018006.2:c.-2-331_-2-328del	XP_016873495.1:n.-2-331_-2-328del
NM_017547.4:c.606_609del MANE Select	NP_060017.1:p.Gly204TrpfsTer?
NR_037647.2:n.438_441del
NR_037648.2:n.783_786del