Canonical Allele Identifier: CA918990477
Gene: FOXRED1 HGNC NCBI

Linked Data

dbSNP Id: rs1555062748

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126271471_126271472dup , CM000673.2:g.126271471_126271472dup GRCh38
NC_000011.9:g.126141366_126141367dup , CM000673.1:g.126141366_126141367dup GRCh37
NC_000011.8:g.125646576_125646577dup NCBI36
NG_028029.1:g.7432_7433dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.298_299dup
ENST00000532101.6:n.297_298dup
ENST00000532125.2:c.120_121dup ENSP00000434178.2:p.Ile41ArgfsTer28
ENST00000533839.6:c.85+2180_85+2181dup ENSP00000509952.1:n.85+2180_85+2181dup
ENST00000534011.6:n.396_397dup
ENST00000685484.1:c.120_121dup ENSP00000510622.1:p.Ile41ArgfsTer28
ENST00000685601.1:c.120_121dup ENSP00000510603.1:p.Ile41ArgfsTer28
ENST00000685765.1:c.120_121dup ENSP00000509991.1:p.Ile41ArgfsTer28
ENST00000685844.1:c.86-1498_86-1497dup ENSP00000509820.1:n.86-1498_86-1497dup
ENST00000685857.1:n.298_299dup
ENST00000686242.1:c.86-1498_86-1497dup ENSP00000508950.1:n.86-1498_86-1497dup
ENST00000686888.1:c.120_121dup ENSP00000509619.1:p.Ile41ArgfsTer28
ENST00000687699.1:c.244_245dup ENSP00000508878.1:n.244_245dup
ENST00000687786.1:n.1453_1454dup
ENST00000688588.1:c.120_121dup ENSP00000510802.1:p.Ile41ArgfsTer28
ENST00000688927.1:n.298_299dup
ENST00000689283.1:c.210-1498_210-1497dup ENSP00000509050.1:n.210-1498_210-1497dup
ENST00000689477.1:c.*13_*14dup ENSP00000508945.1:n.*13_*14dup
ENST00000689765.1:c.86-1498_86-1497dup ENSP00000509625.1:n.86-1498_86-1497dup
ENST00000690512.1:c.86-1007_86-1006dup ENSP00000509793.1:n.86-1007_86-1006dup
ENST00000692039.1:c.206_207dup ENSP00000508821.1:p.Ser70AspfsTer11
ENST00000692336.1:c.120_121dup ENSP00000508540.1:p.Ile41ArgfsTer28
ENST00000693133.1:n.226-1498_226-1497dup
ENST00000263578.10:c.120_121dup MANE Select ENSP00000263578.5:p.Ile41ArgfsTer28
ENST00000263578.9:c.120_121dup ENSP00000263578.5:p.Ile41ArgfsTer28
ENST00000524751.5:n.223-1498_223-1497dup
ENST00000525083.5:n.122-1498_122-1497dup
ENST00000525770.5:c.86-1498_86-1497dup ENSP00000434739.1:n.86-1498_86-1497dup
ENST00000526366.5:n.101-248_101-247dup
ENST00000526525.1:n.246-1498_246-1497dup
ENST00000527004.5:c.120_121dup ENSP00000436374.1:p.Ile41ArgfsTer28
ENST00000529802.1:n.170_171dup
ENST00000532101.5:n.343_344dup
ENST00000532125.1:c.78_79dup ENSP00000434178.1:p.Ile27ArgfsTer28
ENST00000533839.5:n.237+2180_237+2181dup
ENST00000534011.5:n.158-1007_158-1006dup
ENST00000534315.5:n.527_528dup
NM_017547.3:c.120_121dup NP_060017.1:p.Ile41ArgfsTer28
NR_037647.1:n.253-1498_253-1497dup
NR_037648.1:n.306_307dup
XM_006718880.2:c.-419_-418dup XP_006718943.1:n.-419_-418dup
XM_006718881.2:c.-232-1498_-232-1497dup XP_006718944.1:n.-232-1498_-232-1497dup
XM_011542895.1:c.-391_-390dup XP_011541197.1:n.-391_-390dup
XM_011542896.1:c.-411_-410dup XP_011541198.1:n.-411_-410dup
XM_006718881.3:c.-232-1498_-232-1497dup XP_006718944.1:n.-232-1498_-232-1497dup
XM_011542895.2:c.-391_-390dup XP_011541197.1:n.-391_-390dup
XM_011542896.2:c.-411_-410dup XP_011541198.1:n.-411_-410dup
XM_017018000.2:c.120_121dup XP_016873489.1:p.Ile41ArgfsTer28
XM_017018001.1:c.-411_-410dup XP_016873490.1:n.-411_-410dup
XM_017018002.1:c.-224-1498_-224-1497dup XP_016873491.1:n.-224-1498_-224-1497dup
XM_017018003.2:c.-419_-418dup XP_016873492.1:n.-419_-418dup
XM_017018004.1:c.-419_-418dup XP_016873493.1:n.-419_-418dup
XM_017018005.1:c.-617_-616dup XP_016873494.1:n.-617_-616dup
XM_017018006.2:c.-419_-418dup XP_016873495.1:n.-419_-418dup
NM_017547.4:c.120_121dup MANE Select NP_060017.1:p.Ile41ArgfsTer28
NR_037647.2:n.139-1498_139-1497dup
NR_037648.2:n.297_298dup