Canonical Allele Identifier: CA2007076603

Gene: FOXRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126271261_126271262delinsAT , CM000673.2:g.126271261_126271262delinsAT	GRCh38
NC_000011.9:g.126141156_126141157delinsAT , CM000673.1:g.126141156_126141157delinsAT	GRCh37
NC_000011.8:g.125646366_125646367delinsAT	NCBI36
NG_028029.1:g.7222_7223delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.264-176_264-175delinsAT
ENST00000532101.6:n.87_88delinsAT
ENST00000532125.2:c.86-176_86-175delinsAT	ENSP00000434178.2:n.86-176_86-175delinsAT
ENST00000533839.6:c.85+1970_85+1971delinsAT	ENSP00000509952.1:n.85+1970_85+1971delinsAT
ENST00000534011.6:n.186_187delinsAT
ENST00000685484.1:c.86-176_86-175delinsAT	ENSP00000510622.1:n.86-176_86-175delinsAT
ENST00000685601.1:c.86-176_86-175delinsAT	ENSP00000510603.1:n.86-176_86-175delinsAT
ENST00000685765.1:c.86-176_86-175delinsAT	ENSP00000509991.1:n.86-176_86-175delinsAT
ENST00000685844.1:c.86-1708_86-1707delinsAT	ENSP00000509820.1:n.86-1708_86-1707delinsAT
ENST00000685857.1:n.264-176_264-175delinsAT
ENST00000686242.1:c.86-1708_86-1707delinsAT	ENSP00000508950.1:n.86-1708_86-1707delinsAT
ENST00000686888.1:c.86-176_86-175delinsAT	ENSP00000509619.1:n.86-176_86-175delinsAT
ENST00000687699.1:c.210-176_210-175delinsAT	ENSP00000508878.1:n.210-176_210-175delinsAT
ENST00000687786.1:n.1243_1244delinsAT
ENST00000688588.1:c.86-176_86-175delinsAT	ENSP00000510802.1:n.86-176_86-175delinsAT
ENST00000688927.1:n.264-176_264-175delinsAT
ENST00000689283.1:c.210-1708_210-1707delinsAT	ENSP00000509050.1:n.210-1708_210-1707delinsAT
ENST00000689477.1:c.127_128delinsAT	ENSP00000508945.1:p.Ile43=
ENST00000689765.1:c.86-1708_86-1707delinsAT	ENSP00000509625.1:n.86-1708_86-1707delinsAT
ENST00000690512.1:c.86-1217_86-1216delinsAT	ENSP00000509793.1:n.86-1217_86-1216delinsAT
ENST00000692039.1:c.86-90_86-89delinsAT	ENSP00000508821.1:n.86-90_86-89delinsAT
ENST00000692336.1:c.86-176_86-175delinsAT	ENSP00000508540.1:n.86-176_86-175delinsAT
ENST00000693133.1:n.226-1708_226-1707delinsAT
ENST00000263578.10:c.86-176_86-175delinsAT MANE Select	ENSP00000263578.5:n.86-176_86-175delinsAT
ENST00000263578.9:c.86-176_86-175delinsAT	ENSP00000263578.5:n.86-176_86-175delinsAT
ENST00000524751.5:n.223-1708_223-1707delinsAT
ENST00000525083.5:n.122-1708_122-1707delinsAT
ENST00000525770.5:c.86-1708_86-1707delinsAT	ENSP00000434739.1:n.86-1708_86-1707delinsAT
ENST00000526366.5:n.101-458_101-457delinsAT
ENST00000526525.1:n.246-1708_246-1707delinsAT
ENST00000527004.5:c.86-176_86-175delinsAT	ENSP00000436374.1:n.86-176_86-175delinsAT
ENST00000529802.1:n.136-176_136-175delinsAT
ENST00000532101.5:n.133_134delinsAT
ENST00000532125.1:c.44-176_44-175delinsAT	ENSP00000434178.1:n.44-176_44-175delinsAT
ENST00000533839.5:n.237+1970_237+1971delinsAT
ENST00000534011.5:n.158-1217_158-1216delinsAT
ENST00000534315.5:n.317_318delinsAT
NM_017547.3:c.86-176_86-175delinsAT	NP_060017.1:n.86-176_86-175delinsAT
NR_037647.1:n.253-1708_253-1707delinsAT
NR_037648.1:n.272-176_272-175delinsAT
XM_006718880.2:c.-629_-628delinsAT	XP_006718943.1:n.-629_-628delinsAT
XM_006718881.2:c.-232-1708_-232-1707delinsAT	XP_006718944.1:n.-232-1708_-232-1707delinsAT
XM_011542895.1:c.-601_-600delinsAT	XP_011541197.1:n.-601_-600delinsAT
XM_011542896.1:c.-445-176_-445-175delinsAT	XP_011541198.1:n.-445-176_-445-175delinsAT
XM_006718881.3:c.-232-1708_-232-1707delinsAT	XP_006718944.1:n.-232-1708_-232-1707delinsAT
XM_011542895.2:c.-601_-600delinsAT	XP_011541197.1:n.-601_-600delinsAT
XM_011542896.2:c.-445-176_-445-175delinsAT	XP_011541198.1:n.-445-176_-445-175delinsAT
XM_017018000.2:c.86-176_86-175delinsAT	XP_016873489.1:n.86-176_86-175delinsAT
XM_017018001.1:c.-445-176_-445-175delinsAT	XP_016873490.1:n.-445-176_-445-175delinsAT
XM_017018002.1:c.-224-1708_-224-1707delinsAT	XP_016873491.1:n.-224-1708_-224-1707delinsAT
XM_017018003.2:c.-453-176_-453-175delinsAT	XP_016873492.1:n.-453-176_-453-175delinsAT
XM_017018004.1:c.-629_-628delinsAT	XP_016873493.1:n.-629_-628delinsAT
XM_017018005.1:c.-827_-826delinsAT	XP_016873494.1:n.-827_-826delinsAT
XM_017018006.2:c.-453-176_-453-175delinsAT	XP_016873495.1:n.-453-176_-453-175delinsAT
NM_017547.4:c.86-176_86-175delinsAT MANE Select	NP_060017.1:n.86-176_86-175delinsAT
NR_037647.2:n.139-1708_139-1707delinsAT
NR_037648.2:n.263-176_263-175delinsAT