Canonical Allele Identifier: CA230562280
Community Standard Title: NM_017547.4(FOXRED1):c.537-269del
Gene: FOXRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126274658del , CM000673.2:g.126274658del GRCh38
NC_000011.9:g.126144553del , CM000673.1:g.126144553del GRCh37
NC_000011.8:g.125649763del NCBI36
NG_028029.1:g.10619del

Transcript Alleles

HGVS Amino-acid Change
NM_017547.4:c.537-269del MANE Select NP_060017.1:n.537-269del
ENST00000263578.10:c.537-269del MANE Select ENSP00000263578.5:n.537-269del
NM_017547.3:c.537-269del NP_060017.1:n.537-269del
NR_037647.1:n.483-269del
NR_037647.2:n.369-269del
NR_037648.1:n.723-269del
NR_037648.2:n.714-269del
ENST00000263578.9:c.537-269del ENSP00000263578.5:n.537-269del
ENST00000524751.5:n.473-269del
ENST00000525083.5:n.352-669del
ENST00000525083.6:n.715-269del
ENST00000525770.5:c.*169-269del ENSP00000434739.1:n.*169-269del
ENST00000526366.5:n.468-269del
ENST00000527004.5:c.534-669del ENSP00000436374.1:n.534-669del
ENST00000527875.1:n.367-269del
ENST00000530642.1:n.745del
ENST00000532101.5:n.760-269del
ENST00000532101.6:n.734-669del
ENST00000532125.1:c.495-269del ENSP00000434178.1:n.495-269del
ENST00000532125.2:c.534-269del ENSP00000434178.2:n.534-269del
ENST00000533395.5:n.365-669del
ENST00000533839.5:n.238-1136del
ENST00000533839.6:c.86-1136del ENSP00000509952.1:n.86-1136del
ENST00000534011.5:n.593-273del
ENST00000534011.6:n.833-273del
ENST00000534315.5:n.944-669del
ENST00000685484.1:c.537-269del ENSP00000510622.1:n.537-269del
ENST00000685601.1:c.537-269del ENSP00000510603.1:n.537-269del
ENST00000685765.1:c.537-269del ENSP00000509991.1:n.537-269del
ENST00000685844.1:c.*169-669del ENSP00000509820.1:n.*169-669del
ENST00000685857.1:n.971-269del
ENST00000686242.1:c.336-269del ENSP00000508950.1:n.336-269del
ENST00000686888.1:c.*104-269del ENSP00000509619.1:n.*104-269del
ENST00000687699.1:c.661-269del ENSP00000508878.1:n.661-269del
ENST00000687786.1:n.2068-669del
ENST00000688100.1:n.1458-269del
ENST00000688588.1:c.537-269del ENSP00000510802.1:n.537-269del
ENST00000688927.1:n.2174del
ENST00000689283.1:c.*200-269del ENSP00000509050.1:n.*200-269del
ENST00000689477.1:c.*430-269del ENSP00000508945.1:n.*430-269del
ENST00000689765.1:c.*169-713del ENSP00000509625.1:n.*169-713del
ENST00000690512.1:c.*392-273del ENSP00000509793.1:n.*392-273del
ENST00000692039.1:c.*335-269del ENSP00000508821.1:n.*335-269del
ENST00000692336.1:c.561-269del ENSP00000508540.1:n.561-269del
ENST00000693133.1:n.712-269del
XM_006718879.2:c.27-269del XP_006718942.1:n.27-269del
XM_006718879.3:c.27-269del XP_006718942.1:n.27-269del
XM_006718880.2:c.-2-669del XP_006718943.1:n.-2-669del
XM_006718881.2:c.-2-669del XP_006718944.1:n.-2-669del
XM_006718881.3:c.-2-669del XP_006718944.1:n.-2-669del
XM_011542895.1:c.27-269del XP_011541197.1:n.27-269del
XM_011542895.2:c.27-269del XP_011541197.1:n.27-269del
XM_011542896.1:c.27-269del XP_011541198.1:n.27-269del
XM_011542896.2:c.27-269del XP_011541198.1:n.27-269del
XM_017018000.2:c.537-269del XP_016873489.1:n.537-269del
XM_017018001.1:c.27-269del XP_016873490.1:n.27-269del
XM_017018002.1:c.27-269del XP_016873491.1:n.27-269del
XM_017018003.2:c.-2-669del XP_016873492.1:n.-2-669del
XM_017018004.1:c.-2-669del XP_016873493.1:n.-2-669del
XM_017018005.1:c.-2-669del XP_016873494.1:n.-2-669del
XM_017018006.2:c.-2-669del XP_016873495.1:n.-2-669del