Canonical Allele Identifier: CA2616722591
Gene: FOXRED1 HGNC NCBI

Linked Data

gnomAD v4: 11-126275522-A-ACCCCTTTCCCCCTC
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126275522_126275523insCCCCTTTCCCCCTC , CM000673.2:g.126275522_126275523insCCCCTTTCCCCCTC GRCh38
NC_000011.9:g.126145417_126145418insCCCCTTTCCCCCTC , CM000673.1:g.126145417_126145418insCCCCTTTCCCCCTC GRCh37
NC_000011.8:g.125650627_125650628insCCCCTTTCCCCCTC NCBI36
NG_028029.1:g.11483_11484insCCCCTTTCCCCCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.1216+94_1216+95insCCCCTTTCCCCCTC
ENST00000532101.6:n.835+94_835+95insCCCCTTTCCCCCTC
ENST00000532125.2:c.730+94_730+95insCCCCTTTCCCCCTC ENSP00000434178.2:n.730+94_730+95insCCCCTTTCCCCCTC
ENST00000533839.6:c.86-272_86-271insCCCCTTTCCCCCTC ENSP00000509952.1:n.86-272_86-271insCCCCTTTCCCCCTC
ENST00000534011.6:n.1025+94_1025+95insCCCCTTTCCCCCTC
ENST00000685484.1:c.733+94_733+95insCCCCTTTCCCCCTC ENSP00000510622.1:n.733+94_733+95insCCCCTTTCCCCCTC
ENST00000685601.1:c.733+94_733+95insCCCCTTTCCCCCTC ENSP00000510603.1:n.733+94_733+95insCCCCTTTCCCCCTC
ENST00000685765.1:c.733+94_733+95insCCCCTTTCCCCCTC ENSP00000509991.1:n.733+94_733+95insCCCCTTTCCCCCTC
ENST00000685844.1:c.*270+94_*270+95insCCCCTTTCCCCCTC ENSP00000509820.1:n.*270+94_*270+95insCCCCTTTCCCCCTC
ENST00000685857.1:n.1566_1567insCCCCTTTCCCCCTC
ENST00000686242.1:c.532+94_532+95insCCCCTTTCCCCCTC ENSP00000508950.1:n.532+94_532+95insCCCCTTTCCCCCTC
ENST00000686888.1:c.*300+94_*300+95insCCCCTTTCCCCCTC ENSP00000509619.1:n.*300+94_*300+95insCCCCTTTCCCCCTC
ENST00000687699.1:c.857+94_857+95insCCCCTTTCCCCCTC ENSP00000508878.1:n.857+94_857+95insCCCCTTTCCCCCTC
ENST00000687786.1:n.2169+94_2169+95insCCCCTTTCCCCCTC
ENST00000688100.1:n.1654+94_1654+95insCCCCTTTCCCCCTC
ENST00000688588.1:c.733+94_733+95insCCCCTTTCCCCCTC ENSP00000510802.1:n.733+94_733+95insCCCCTTTCCCCCTC
ENST00000688927.1:n.2944+94_2944+95insCCCCTTTCCCCCTC
ENST00000689283.1:c.*396+94_*396+95insCCCCTTTCCCCCTC ENSP00000509050.1:n.*396+94_*396+95insCCCCTTTCCCCCTC
ENST00000689477.1:c.*626+94_*626+95insCCCCTTTCCCCCTC ENSP00000508945.1:n.*626+94_*626+95insCCCCTTTCCCCCTC
ENST00000689765.1:c.*226+94_*226+95insCCCCTTTCCCCCTC ENSP00000509625.1:n.*226+94_*226+95insCCCCTTTCCCCCTC
ENST00000690512.1:c.*584+94_*584+95insCCCCTTTCCCCCTC ENSP00000509793.1:n.*584+94_*584+95insCCCCTTTCCCCCTC
ENST00000692039.1:c.*531+94_*531+95insCCCCTTTCCCCCTC ENSP00000508821.1:n.*531+94_*531+95insCCCCTTTCCCCCTC
ENST00000692336.1:c.757+94_757+95insCCCCTTTCCCCCTC ENSP00000508540.1:n.757+94_757+95insCCCCTTTCCCCCTC
ENST00000693133.1:n.1307_1308insCCCCTTTCCCCCTC
ENST00000263578.10:c.733+94_733+95insCCCCTTTCCCCCTC MANE Select ENSP00000263578.5:n.733+94_733+95insCCCCTTTCCCCCTC
ENST00000263578.9:c.733+94_733+95insCCCCTTTCCCCCTC ENSP00000263578.5:n.733+94_733+95insCCCCTTTCCCCCTC
ENST00000525083.5:n.453+94_453+95insCCCCTTTCCCCCTC
ENST00000525770.5:c.*365+94_*365+95insCCCCTTTCCCCCTC ENSP00000434739.1:n.*365+94_*365+95insCCCCTTTCCCCCTC
ENST00000527004.5:c.*77+94_*77+95insCCCCTTTCCCCCTC ENSP00000436374.1:n.*77+94_*77+95insCCCCTTTCCCCCTC
ENST00000530642.1:n.1609_1610insCCCCTTTCCCCCTC
ENST00000532101.5:n.956+94_956+95insCCCCTTTCCCCCTC
ENST00000532125.1:c.691+94_691+95insCCCCTTTCCCCCTC ENSP00000434178.1:n.691+94_691+95insCCCCTTTCCCCCTC
ENST00000533395.5:n.466+94_466+95insCCCCTTTCCCCCTC
ENST00000533839.5:n.238-272_238-271insCCCCTTTCCCCCTC
ENST00000534011.5:n.785+94_785+95insCCCCTTTCCCCCTC
ENST00000534315.5:n.1045+94_1045+95insCCCCTTTCCCCCTC
NM_017547.3:c.733+94_733+95insCCCCTTTCCCCCTC NP_060017.1:n.733+94_733+95insCCCCTTTCCCCCTC
NR_037647.1:n.679+94_679+95insCCCCTTTCCCCCTC
NR_037648.1:n.919+94_919+95insCCCCTTTCCCCCTC
XM_006718879.2:c.223+94_223+95insCCCCTTTCCCCCTC XP_006718942.1:n.223+94_223+95insCCCCTTTCCCCCTC
XM_006718880.2:c.100+94_100+95insCCCCTTTCCCCCTC XP_006718943.1:n.100+94_100+95insCCCCTTTCCCCCTC
XM_006718881.2:c.100+94_100+95insCCCCTTTCCCCCTC XP_006718944.1:n.100+94_100+95insCCCCTTTCCCCCTC
XM_011542895.1:c.223+94_223+95insCCCCTTTCCCCCTC XP_011541197.1:n.223+94_223+95insCCCCTTTCCCCCTC
XM_011542896.1:c.223+94_223+95insCCCCTTTCCCCCTC XP_011541198.1:n.223+94_223+95insCCCCTTTCCCCCTC
XM_006718879.3:c.223+94_223+95insCCCCTTTCCCCCTC XP_006718942.1:n.223+94_223+95insCCCCTTTCCCCCTC
XM_006718881.3:c.100+94_100+95insCCCCTTTCCCCCTC XP_006718944.1:n.100+94_100+95insCCCCTTTCCCCCTC
XM_011542895.2:c.223+94_223+95insCCCCTTTCCCCCTC XP_011541197.1:n.223+94_223+95insCCCCTTTCCCCCTC
XM_011542896.2:c.223+94_223+95insCCCCTTTCCCCCTC XP_011541198.1:n.223+94_223+95insCCCCTTTCCCCCTC
XM_017018000.2:c.733+94_733+95insCCCCTTTCCCCCTC XP_016873489.1:n.733+94_733+95insCCCCTTTCCCCCTC
XM_017018001.1:c.223+94_223+95insCCCCTTTCCCCCTC XP_016873490.1:n.223+94_223+95insCCCCTTTCCCCCTC
XM_017018002.1:c.223+94_223+95insCCCCTTTCCCCCTC XP_016873491.1:n.223+94_223+95insCCCCTTTCCCCCTC
XM_017018003.2:c.100+94_100+95insCCCCTTTCCCCCTC XP_016873492.1:n.100+94_100+95insCCCCTTTCCCCCTC
XM_017018004.1:c.100+94_100+95insCCCCTTTCCCCCTC XP_016873493.1:n.100+94_100+95insCCCCTTTCCCCCTC
XM_017018005.1:c.100+94_100+95insCCCCTTTCCCCCTC XP_016873494.1:n.100+94_100+95insCCCCTTTCCCCCTC
XM_017018006.2:c.100+94_100+95insCCCCTTTCCCCCTC XP_016873495.1:n.100+94_100+95insCCCCTTTCCCCCTC
NM_017547.4:c.733+94_733+95insCCCCTTTCCCCCTC MANE Select NP_060017.1:n.733+94_733+95insCCCCTTTCCCCCTC
NR_037647.2:n.565+94_565+95insCCCCTTTCCCCCTC
NR_037648.2:n.910+94_910+95insCCCCTTTCCCCCTC
Search 100 bp 5'
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