Canonical Allele Identifier: CA6354155
Gene: FOXRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2757693
ClinVar RCV Id: RCV003567350
dbSNP Id: rs750646991

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126275311_126275312del , CM000673.2:g.126275311_126275312del GRCh38
NC_000011.9:g.126145206_126145207del , CM000673.1:g.126145206_126145207del GRCh37
NC_000011.8:g.125650416_125650417del NCBI36
NG_028029.1:g.11272_11273del

Transcript Alleles

HGVS Amino-acid change
ENST00000525083.6:n.1099_1100del
ENST00000532101.6:n.734-16_734-15del
ENST00000532125.2:c.629-16_629-15del ENSP00000434178.2:n.629-16_629-15del
ENST00000533839.6:c.86-483_86-482del ENSP00000509952.1:n.86-483_86-482del
ENST00000534011.6:n.924-16_924-15del
ENST00000685484.1:c.632-16_632-15del ENSP00000510622.1:n.632-16_632-15del
ENST00000685601.1:c.632-16_632-15del ENSP00000510603.1:n.632-16_632-15del
ENST00000685765.1:c.632-16_632-15del ENSP00000509991.1:n.632-16_632-15del
ENST00000685844.1:c.*169-16_*169-15del ENSP00000509820.1:n.*169-16_*169-15del
ENST00000685857.1:n.1355_1356del
ENST00000686242.1:c.431-16_431-15del ENSP00000508950.1:n.431-16_431-15del
ENST00000686888.1:c.*199-16_*199-15del ENSP00000509619.1:n.*199-16_*199-15del
ENST00000687699.1:c.756-16_756-15del ENSP00000508878.1:n.756-16_756-15del
ENST00000687786.1:n.2068-16_2068-15del
ENST00000688100.1:n.1553-16_1553-15del
ENST00000688588.1:c.632-16_632-15del ENSP00000510802.1:n.632-16_632-15del
ENST00000688927.1:n.2827_2828del
ENST00000689283.1:c.*295-16_*295-15del ENSP00000509050.1:n.*295-16_*295-15del
ENST00000689477.1:c.*525-16_*525-15del ENSP00000508945.1:n.*525-16_*525-15del
ENST00000689765.1:c.*169-60_*169-59del ENSP00000509625.1:n.*169-60_*169-59del
ENST00000690512.1:c.*483-16_*483-15del ENSP00000509793.1:n.*483-16_*483-15del
ENST00000692039.1:c.*430-16_*430-15del ENSP00000508821.1:n.*430-16_*430-15del
ENST00000692336.1:c.656-16_656-15del ENSP00000508540.1:n.656-16_656-15del
ENST00000693133.1:n.1096_1097del
ENST00000263578.10:c.632-16_632-15del MANE Select ENSP00000263578.5:n.632-16_632-15del
ENST00000263578.9:c.632-16_632-15del ENSP00000263578.5:n.632-16_632-15del
ENST00000524751.5:n.857_858del
ENST00000525083.5:n.352-16_352-15del
ENST00000525770.5:c.*264-16_*264-15del ENSP00000434739.1:n.*264-16_*264-15del
ENST00000527004.5:c.534-16_534-15del ENSP00000436374.1:n.534-16_534-15del
ENST00000530642.1:n.1398_1399del
ENST00000532101.5:n.855-16_855-15del
ENST00000532125.1:c.590-16_590-15del ENSP00000434178.1:n.590-16_590-15del
ENST00000533395.5:n.365-16_365-15del
ENST00000533839.5:n.238-483_238-482del
ENST00000534011.5:n.684-16_684-15del
ENST00000534315.5:n.944-16_944-15del
NM_017547.3:c.632-16_632-15del NP_060017.1:n.632-16_632-15del
NR_037647.1:n.578-16_578-15del
NR_037648.1:n.818-16_818-15del
XM_006718879.2:c.122-16_122-15del XP_006718942.1:n.122-16_122-15del
XM_006718880.2:c.-2-16_-2-15del XP_006718943.1:n.-2-16_-2-15del
XM_006718881.2:c.-2-16_-2-15del XP_006718944.1:n.-2-16_-2-15del
XM_011542895.1:c.122-16_122-15del XP_011541197.1:n.122-16_122-15del
XM_011542896.1:c.122-16_122-15del XP_011541198.1:n.122-16_122-15del
XM_006718879.3:c.122-16_122-15del XP_006718942.1:n.122-16_122-15del
XM_006718881.3:c.-2-16_-2-15del XP_006718944.1:n.-2-16_-2-15del
XM_011542895.2:c.122-16_122-15del XP_011541197.1:n.122-16_122-15del
XM_011542896.2:c.122-16_122-15del XP_011541198.1:n.122-16_122-15del
XM_017018000.2:c.632-16_632-15del XP_016873489.1:n.632-16_632-15del
XM_017018001.1:c.122-16_122-15del XP_016873490.1:n.122-16_122-15del
XM_017018002.1:c.122-16_122-15del XP_016873491.1:n.122-16_122-15del
XM_017018003.2:c.-2-16_-2-15del XP_016873492.1:n.-2-16_-2-15del
XM_017018004.1:c.-2-16_-2-15del XP_016873493.1:n.-2-16_-2-15del
XM_017018005.1:c.-2-16_-2-15del XP_016873494.1:n.-2-16_-2-15del
XM_017018006.2:c.-2-16_-2-15del XP_016873495.1:n.-2-16_-2-15del
NM_017547.4:c.632-16_632-15del MANE Select NP_060017.1:n.632-16_632-15del
NR_037647.2:n.464-16_464-15del
NR_037648.2:n.809-16_809-15del