Canonical Allele Identifier: CA2575022776

Gene: FOXRED1

Linked Data

• gnomAD v4: 11-126275346-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275349del , CM000673.2:g.126275349del	GRCh38
NC_000011.9:g.126145244del , CM000673.1:g.126145244del	GRCh37
NC_000011.8:g.125650454del	NCBI36
NG_028029.1:g.11310del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1137del
ENST00000532101.6:n.756del
ENST00000532125.2:c.651del	ENSP00000434178.2:p.Phe217LeufsTer26
ENST00000533839.6:c.86-445del	ENSP00000509952.1:n.86-445del
ENST00000534011.6:n.946del
ENST00000685484.1:c.654del	ENSP00000510622.1:p.Phe218LeufsTer26
ENST00000685601.1:c.654del	ENSP00000510603.1:p.Phe218LeufsTer26
ENST00000685765.1:c.654del	ENSP00000509991.1:p.Phe218LeufsTer26
ENST00000685844.1:c.*191del	ENSP00000509820.1:n.*191del
ENST00000685857.1:n.1393del
ENST00000686242.1:c.453del	ENSP00000508950.1:n.453del
ENST00000686888.1:c.*221del	ENSP00000509619.1:n.*221del
ENST00000687699.1:c.778del	ENSP00000508878.1:n.778del
ENST00000687786.1:n.2090del
ENST00000688100.1:n.1575del
ENST00000688588.1:c.654del	ENSP00000510802.1:p.Phe218LeufsTer26
ENST00000688927.1:n.2865del
ENST00000689283.1:c.*317del	ENSP00000509050.1:n.*317del
ENST00000689477.1:c.*547del	ENSP00000508945.1:n.*547del
ENST00000689765.1:c.*169-22del	ENSP00000509625.1:n.*169-22del
ENST00000690512.1:c.*505del	ENSP00000509793.1:n.*505del
ENST00000692039.1:c.*452del	ENSP00000508821.1:n.*452del
ENST00000692336.1:c.678del	ENSP00000508540.1:p.Phe226LeufsTer26
ENST00000693133.1:n.1134del
ENST00000263578.10:c.654del MANE Select	ENSP00000263578.5:p.Phe218LeufsTer26
ENST00000263578.9:c.654del	ENSP00000263578.5:p.Phe218LeufsTer26
ENST00000524751.5:n.895del
ENST00000525083.5:n.374del
ENST00000525770.5:c.*286del	ENSP00000434739.1:n.*286del
ENST00000527004.5:c.556del	ENSP00000436374.1:p.Ter186AspextTer?
ENST00000530642.1:n.1436del
ENST00000532101.5:n.877del
ENST00000532125.1:c.612del	ENSP00000434178.1:p.Phe204LeufsTer26
ENST00000533395.5:n.387del
ENST00000533839.5:n.238-445del
ENST00000534011.5:n.706del
ENST00000534315.5:n.966del
NM_017547.3:c.654del	NP_060017.1:p.Phe218LeufsTer26
NR_037647.1:n.600del
NR_037648.1:n.840del
XM_006718879.2:c.144del	XP_006718942.1:p.Phe48LeufsTer26
XM_006718880.2:c.21del	XP_006718943.1:p.Phe7LeufsTer26
XM_006718881.2:c.21del	XP_006718944.1:p.Phe7LeufsTer26
XM_011542895.1:c.144del	XP_011541197.1:p.Phe48LeufsTer26
XM_011542896.1:c.144del	XP_011541198.1:p.Phe48LeufsTer26
XM_006718879.3:c.144del	XP_006718942.1:p.Phe48LeufsTer26
XM_006718881.3:c.21del	XP_006718944.1:p.Phe7LeufsTer26
XM_011542895.2:c.144del	XP_011541197.1:p.Phe48LeufsTer26
XM_011542896.2:c.144del	XP_011541198.1:p.Phe48LeufsTer26
XM_017018000.2:c.654del	XP_016873489.1:p.Phe218LeufsTer26
XM_017018001.1:c.144del	XP_016873490.1:p.Phe48LeufsTer26
XM_017018002.1:c.144del	XP_016873491.1:p.Phe48LeufsTer26
XM_017018003.2:c.21del	XP_016873492.1:p.Phe7LeufsTer26
XM_017018004.1:c.21del	XP_016873493.1:p.Phe7LeufsTer26
XM_017018005.1:c.21del	XP_016873494.1:p.Phe7LeufsTer26
XM_017018006.2:c.21del	XP_016873495.1:p.Phe7LeufsTer26
NM_017547.4:c.654del MANE Select	NP_060017.1:p.Phe218LeufsTer26
NR_037647.2:n.486del
NR_037648.2:n.831del