Canonical Allele Identifier: CA2007076825
Gene: FOXRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126271524_126271528delinsACCTG , CM000673.2:g.126271524_126271528delinsACCTG GRCh38
NC_000011.9:g.126141419_126141423delinsACCTG , CM000673.1:g.126141419_126141423delinsACCTG GRCh37
NC_000011.8:g.125646629_125646633delinsACCTG NCBI36
NG_028029.1:g.7485_7489delinsACCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.351_355delinsACCTG
ENST00000532101.6:n.350_354delinsACCTG
ENST00000532125.2:c.173_177delinsACCTG ENSP00000434178.2:p.His58=
ENST00000533839.6:c.85+2233_85+2237delinsACCTG ENSP00000509952.1:n.85+2233_85+2237delinsACCTG
ENST00000534011.6:n.449_453delinsACCTG
ENST00000685484.1:c.173_177delinsACCTG ENSP00000510622.1:p.His58=
ENST00000685601.1:c.173_177delinsACCTG ENSP00000510603.1:p.His58=
ENST00000685765.1:c.173_177delinsACCTG ENSP00000509991.1:p.His58=
ENST00000685844.1:c.86-1445_86-1441delinsACCTG ENSP00000509820.1:n.86-1445_86-1441delinsACCTG
ENST00000685857.1:n.351_355delinsACCTG
ENST00000686242.1:c.86-1445_86-1441delinsACCTG ENSP00000508950.1:n.86-1445_86-1441delinsACCTG
ENST00000686888.1:c.173_177delinsACCTG ENSP00000509619.1:p.His58=
ENST00000687699.1:c.297_301delinsACCTG ENSP00000508878.1:n.297_301delinsACCTG
ENST00000687786.1:n.1506_1510delinsACCTG
ENST00000688588.1:c.173_177delinsACCTG ENSP00000510802.1:p.His58=
ENST00000688927.1:n.351_355delinsACCTG
ENST00000689283.1:c.210-1445_210-1441delinsACCTG ENSP00000509050.1:n.210-1445_210-1441delinsACCTG
ENST00000689477.1:c.*66_*70delinsACCTG ENSP00000508945.1:n.*66_*70delinsACCTG
ENST00000689765.1:c.86-1445_86-1441delinsACCTG ENSP00000509625.1:n.86-1445_86-1441delinsACCTG
ENST00000690512.1:c.86-954_86-950delinsACCTG ENSP00000509793.1:n.86-954_86-950delinsACCTG
ENST00000692039.1:c.259_263delinsACCTG ENSP00000508821.1:p.Thr87=
ENST00000692336.1:c.173_177delinsACCTG ENSP00000508540.1:p.His58=
ENST00000693133.1:n.226-1445_226-1441delinsACCTG
ENST00000263578.10:c.173_177delinsACCTG MANE Select ENSP00000263578.5:p.His58=
ENST00000263578.9:c.173_177delinsACCTG ENSP00000263578.5:p.His58=
ENST00000524751.5:n.223-1445_223-1441delinsACCTG
ENST00000525083.5:n.122-1445_122-1441delinsACCTG
ENST00000525770.5:c.86-1445_86-1441delinsACCTG ENSP00000434739.1:n.86-1445_86-1441delinsACCTG
ENST00000526366.5:n.101-195_101-191delinsACCTG
ENST00000526525.1:n.246-1445_246-1441delinsACCTG
ENST00000527004.5:c.173_177delinsACCTG ENSP00000436374.1:p.His58=
ENST00000529802.1:n.223_227delinsACCTG
ENST00000532101.5:n.396_400delinsACCTG
ENST00000532125.1:c.131_135delinsACCTG ENSP00000434178.1:p.His44=
ENST00000533839.5:n.237+2233_237+2237delinsACCTG
ENST00000534011.5:n.158-954_158-950delinsACCTG
ENST00000534315.5:n.580_584delinsACCTG
NM_017547.3:c.173_177delinsACCTG NP_060017.1:p.His58=
NR_037647.1:n.253-1445_253-1441delinsACCTG
NR_037648.1:n.359_363delinsACCTG
XM_006718880.2:c.-366_-362delinsACCTG XP_006718943.1:n.-366_-362delinsACCTG
XM_006718881.2:c.-232-1445_-232-1441delinsACCTG XP_006718944.1:n.-232-1445_-232-1441delinsACCTG
XM_011542895.1:c.-338_-334delinsACCTG XP_011541197.1:n.-338_-334delinsACCTG
XM_011542896.1:c.-358_-354delinsACCTG XP_011541198.1:n.-358_-354delinsACCTG
XM_006718881.3:c.-232-1445_-232-1441delinsACCTG XP_006718944.1:n.-232-1445_-232-1441delinsACCTG
XM_011542895.2:c.-338_-334delinsACCTG XP_011541197.1:n.-338_-334delinsACCTG
XM_011542896.2:c.-358_-354delinsACCTG XP_011541198.1:n.-358_-354delinsACCTG
XM_017018000.2:c.173_177delinsACCTG XP_016873489.1:p.His58=
XM_017018001.1:c.-358_-354delinsACCTG XP_016873490.1:n.-358_-354delinsACCTG
XM_017018002.1:c.-224-1445_-224-1441delinsACCTG XP_016873491.1:n.-224-1445_-224-1441delinsACCTG
XM_017018003.2:c.-366_-362delinsACCTG XP_016873492.1:n.-366_-362delinsACCTG
XM_017018004.1:c.-366_-362delinsACCTG XP_016873493.1:n.-366_-362delinsACCTG
XM_017018005.1:c.-564_-560delinsACCTG XP_016873494.1:n.-564_-560delinsACCTG
XM_017018006.2:c.-366_-362delinsACCTG XP_016873495.1:n.-366_-362delinsACCTG
NM_017547.4:c.173_177delinsACCTG MANE Select NP_060017.1:p.His58=
NR_037647.2:n.139-1445_139-1441delinsACCTG
NR_037648.2:n.350_354delinsACCTG