Canonical Allele Identifier: CA673003917
Gene: FOXRED1 HGNC NCBI

Linked Data

dbSNP Id: rs1398488660

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126275494_126275497del , CM000673.2:g.126275494_126275497del GRCh38
NC_000011.9:g.126145389_126145392del , CM000673.1:g.126145389_126145392del GRCh37
NC_000011.8:g.125650599_125650602del NCBI36
NG_028029.1:g.11455_11458del

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.1216+66_1216+69del
ENST00000532101.6:n.835+66_835+69del
ENST00000532125.2:c.730+66_730+69del ENSP00000434178.2:n.730+66_730+69del
ENST00000533839.6:c.86-300_86-297del ENSP00000509952.1:n.86-300_86-297del
ENST00000534011.6:n.1025+66_1025+69del
ENST00000685484.1:c.733+66_733+69del ENSP00000510622.1:n.733+66_733+69del
ENST00000685601.1:c.733+66_733+69del ENSP00000510603.1:n.733+66_733+69del
ENST00000685765.1:c.733+66_733+69del ENSP00000509991.1:n.733+66_733+69del
ENST00000685844.1:c.*270+66_*270+69del ENSP00000509820.1:n.*270+66_*270+69del
ENST00000685857.1:n.1538_1541del
ENST00000686242.1:c.532+66_532+69del ENSP00000508950.1:n.532+66_532+69del
ENST00000686888.1:c.*300+66_*300+69del ENSP00000509619.1:n.*300+66_*300+69del
ENST00000687699.1:c.857+66_857+69del ENSP00000508878.1:n.857+66_857+69del
ENST00000687786.1:n.2169+66_2169+69del
ENST00000688100.1:n.1654+66_1654+69del
ENST00000688588.1:c.733+66_733+69del ENSP00000510802.1:n.733+66_733+69del
ENST00000688927.1:n.2944+66_2944+69del
ENST00000689283.1:c.*396+66_*396+69del ENSP00000509050.1:n.*396+66_*396+69del
ENST00000689477.1:c.*626+66_*626+69del ENSP00000508945.1:n.*626+66_*626+69del
ENST00000689765.1:c.*226+66_*226+69del ENSP00000509625.1:n.*226+66_*226+69del
ENST00000690512.1:c.*584+66_*584+69del ENSP00000509793.1:n.*584+66_*584+69del
ENST00000692039.1:c.*531+66_*531+69del ENSP00000508821.1:n.*531+66_*531+69del
ENST00000692336.1:c.757+66_757+69del ENSP00000508540.1:n.757+66_757+69del
ENST00000693133.1:n.1279_1282del
ENST00000263578.10:c.733+66_733+69del MANE Select ENSP00000263578.5:n.733+66_733+69del
ENST00000263578.9:c.733+66_733+69del ENSP00000263578.5:n.733+66_733+69del
ENST00000525083.5:n.453+66_453+69del
ENST00000525770.5:c.*365+66_*365+69del ENSP00000434739.1:n.*365+66_*365+69del
ENST00000527004.5:c.*77+66_*77+69del ENSP00000436374.1:n.*77+66_*77+69del
ENST00000530642.1:n.1581_1584del
ENST00000532101.5:n.956+66_956+69del
ENST00000532125.1:c.691+66_691+69del ENSP00000434178.1:n.691+66_691+69del
ENST00000533395.5:n.466+66_466+69del
ENST00000533839.5:n.238-300_238-297del
ENST00000534011.5:n.785+66_785+69del
ENST00000534315.5:n.1045+66_1045+69del
NM_017547.3:c.733+66_733+69del NP_060017.1:n.733+66_733+69del
NR_037647.1:n.679+66_679+69del
NR_037648.1:n.919+66_919+69del
XM_006718879.2:c.223+66_223+69del XP_006718942.1:n.223+66_223+69del
XM_006718880.2:c.100+66_100+69del XP_006718943.1:n.100+66_100+69del
XM_006718881.2:c.100+66_100+69del XP_006718944.1:n.100+66_100+69del
XM_011542895.1:c.223+66_223+69del XP_011541197.1:n.223+66_223+69del
XM_011542896.1:c.223+66_223+69del XP_011541198.1:n.223+66_223+69del
XM_006718879.3:c.223+66_223+69del XP_006718942.1:n.223+66_223+69del
XM_006718881.3:c.100+66_100+69del XP_006718944.1:n.100+66_100+69del
XM_011542895.2:c.223+66_223+69del XP_011541197.1:n.223+66_223+69del
XM_011542896.2:c.223+66_223+69del XP_011541198.1:n.223+66_223+69del
XM_017018000.2:c.733+66_733+69del XP_016873489.1:n.733+66_733+69del
XM_017018001.1:c.223+66_223+69del XP_016873490.1:n.223+66_223+69del
XM_017018002.1:c.223+66_223+69del XP_016873491.1:n.223+66_223+69del
XM_017018003.2:c.100+66_100+69del XP_016873492.1:n.100+66_100+69del
XM_017018004.1:c.100+66_100+69del XP_016873493.1:n.100+66_100+69del
XM_017018005.1:c.100+66_100+69del XP_016873494.1:n.100+66_100+69del
XM_017018006.2:c.100+66_100+69del XP_016873495.1:n.100+66_100+69del
NM_017547.4:c.733+66_733+69del MANE Select NP_060017.1:n.733+66_733+69del
NR_037647.2:n.565+66_565+69del
NR_037648.2:n.910+66_910+69del