Canonical Allele Identifier: CA2007079687
Gene: FOXRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126275317_126275320delinsCTTA , CM000673.2:g.126275317_126275320delinsCTTA GRCh38
NC_000011.9:g.126145212_126145215delinsCTTA , CM000673.1:g.126145212_126145215delinsCTTA GRCh37
NC_000011.8:g.125650422_125650425delinsCTTA NCBI36
NG_028029.1:g.11278_11281delinsCTTA

Transcript Alleles

HGVS Amino-acid change
ENST00000525083.6:n.1105_1108delinsCTTA
ENST00000532101.6:n.734-10_734-7delinsCTTA
ENST00000532125.2:c.629-10_629-7delinsCTTA ENSP00000434178.2:n.629-10_629-7delinsCTT...
ENST00000533839.6:c.86-477_86-474delinsCTTA ENSP00000509952.1:n.86-477_86-474delinsCT...
ENST00000534011.6:n.924-10_924-7delinsCTTA
ENST00000685484.1:c.632-10_632-7delinsCTTA ENSP00000510622.1:n.632-10_632-7delinsCTT...
ENST00000685601.1:c.632-10_632-7delinsCTTA ENSP00000510603.1:n.632-10_632-7delinsCTT...
ENST00000685765.1:c.632-10_632-7delinsCTTA ENSP00000509991.1:n.632-10_632-7delinsCTT...
ENST00000685844.1:c.*169-10_*169-7delinsCTTA ENSP00000509820.1:n.*169-10_*169-7delinsC...
ENST00000685857.1:n.1361_1364delinsCTTA
ENST00000686242.1:c.431-10_431-7delinsCTTA ENSP00000508950.1:n.431-10_431-7delinsCTT...
ENST00000686888.1:c.*199-10_*199-7delinsCTTA ENSP00000509619.1:n.*199-10_*199-7delinsC...
ENST00000687699.1:c.756-10_756-7delinsCTTA ENSP00000508878.1:n.756-10_756-7delinsCTT...
ENST00000687786.1:n.2068-10_2068-7delinsCTTA
ENST00000688100.1:n.1553-10_1553-7delinsCTTA
ENST00000688588.1:c.632-10_632-7delinsCTTA ENSP00000510802.1:n.632-10_632-7delinsCTT...
ENST00000688927.1:n.2833_2836delinsCTTA
ENST00000689283.1:c.*295-10_*295-7delinsCTTA ENSP00000509050.1:n.*295-10_*295-7delinsC...
ENST00000689477.1:c.*525-10_*525-7delinsCTTA ENSP00000508945.1:n.*525-10_*525-7delinsC...
ENST00000689765.1:c.*169-54_*169-51delinsCTTA ENSP00000509625.1:n.*169-54_*169-51delins...
ENST00000690512.1:c.*483-10_*483-7delinsCTTA ENSP00000509793.1:n.*483-10_*483-7delinsC...
ENST00000692039.1:c.*430-10_*430-7delinsCTTA ENSP00000508821.1:n.*430-10_*430-7delinsC...
ENST00000692336.1:c.656-10_656-7delinsCTTA ENSP00000508540.1:n.656-10_656-7delinsCTT...
ENST00000693133.1:n.1102_1105delinsCTTA
ENST00000263578.10:c.632-10_632-7delinsCTTA MANE Select ENSP00000263578.5:n.632-10_632-7delinsCTT...
ENST00000263578.9:c.632-10_632-7delinsCTTA ENSP00000263578.5:n.632-10_632-7delinsCTT...
ENST00000524751.5:n.863_866delinsCTTA
ENST00000525083.5:n.352-10_352-7delinsCTTA
ENST00000525770.5:c.*264-10_*264-7delinsCTTA ENSP00000434739.1:n.*264-10_*264-7delinsC...
ENST00000527004.5:c.534-10_534-7delinsCTTA ENSP00000436374.1:n.534-10_534-7delinsCTT...
ENST00000530642.1:n.1404_1407delinsCTTA
ENST00000532101.5:n.855-10_855-7delinsCTTA
ENST00000532125.1:c.590-10_590-7delinsCTTA ENSP00000434178.1:n.590-10_590-7delinsCTT...
ENST00000533395.5:n.365-10_365-7delinsCTTA
ENST00000533839.5:n.238-477_238-474delinsCTTA
ENST00000534011.5:n.684-10_684-7delinsCTTA
ENST00000534315.5:n.944-10_944-7delinsCTTA
NM_017547.3:c.632-10_632-7delinsCTTA NP_060017.1:n.632-10_632-7delinsCTTA
NR_037647.1:n.578-10_578-7delinsCTTA
NR_037648.1:n.818-10_818-7delinsCTTA
XM_006718879.2:c.122-10_122-7delinsCTTA XP_006718942.1:n.122-10_122-7delinsCTTA
XM_006718880.2:c.-2-10_-2-7delinsCTTA XP_006718943.1:n.-2-10_-2-7delinsCTTA
XM_006718881.2:c.-2-10_-2-7delinsCTTA XP_006718944.1:n.-2-10_-2-7delinsCTTA
XM_011542895.1:c.122-10_122-7delinsCTTA XP_011541197.1:n.122-10_122-7delinsCTTA
XM_011542896.1:c.122-10_122-7delinsCTTA XP_011541198.1:n.122-10_122-7delinsCTTA
XM_006718879.3:c.122-10_122-7delinsCTTA XP_006718942.1:n.122-10_122-7delinsCTTA
XM_006718881.3:c.-2-10_-2-7delinsCTTA XP_006718944.1:n.-2-10_-2-7delinsCTTA
XM_011542895.2:c.122-10_122-7delinsCTTA XP_011541197.1:n.122-10_122-7delinsCTTA
XM_011542896.2:c.122-10_122-7delinsCTTA XP_011541198.1:n.122-10_122-7delinsCTTA
XM_017018000.2:c.632-10_632-7delinsCTTA XP_016873489.1:n.632-10_632-7delinsCTTA
XM_017018001.1:c.122-10_122-7delinsCTTA XP_016873490.1:n.122-10_122-7delinsCTTA
XM_017018002.1:c.122-10_122-7delinsCTTA XP_016873491.1:n.122-10_122-7delinsCTTA
XM_017018003.2:c.-2-10_-2-7delinsCTTA XP_016873492.1:n.-2-10_-2-7delinsCTTA
XM_017018004.1:c.-2-10_-2-7delinsCTTA XP_016873493.1:n.-2-10_-2-7delinsCTTA
XM_017018005.1:c.-2-10_-2-7delinsCTTA XP_016873494.1:n.-2-10_-2-7delinsCTTA
XM_017018006.2:c.-2-10_-2-7delinsCTTA XP_016873495.1:n.-2-10_-2-7delinsCTTA
NM_017547.4:c.632-10_632-7delinsCTTA MANE Select NP_060017.1:n.632-10_632-7delinsCTTA
NR_037647.2:n.464-10_464-7delinsCTTA
NR_037648.2:n.809-10_809-7delinsCTTA