Canonical Allele Identifier: CA2616727386

Gene: FOXRED1

Linked Data

• gnomAD v4: 11-126271240-G-GGT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126271240_126271241insGT , CM000673.2:g.126271240_126271241insGT	GRCh38
NC_000011.9:g.126141135_126141136insGT , CM000673.1:g.126141135_126141136insGT	GRCh37
NC_000011.8:g.125646345_125646346insGT	NCBI36
NG_028029.1:g.7201_7202insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.264-197_264-196insGT
ENST00000532101.6:n.66_67insGT
ENST00000532125.2:c.86-197_86-196insGT	ENSP00000434178.2:n.86-197_86-196insGT
ENST00000533839.6:c.85+1949_85+1950insGT	ENSP00000509952.1:n.85+1949_85+1950insGT
ENST00000534011.6:n.165_166insGT
ENST00000685484.1:c.86-197_86-196insGT	ENSP00000510622.1:n.86-197_86-196insGT
ENST00000685601.1:c.86-197_86-196insGT	ENSP00000510603.1:n.86-197_86-196insGT
ENST00000685765.1:c.86-197_86-196insGT	ENSP00000509991.1:n.86-197_86-196insGT
ENST00000685844.1:c.86-1729_86-1728insGT	ENSP00000509820.1:n.86-1729_86-1728insGT
ENST00000685857.1:n.264-197_264-196insGT
ENST00000686242.1:c.86-1729_86-1728insGT	ENSP00000508950.1:n.86-1729_86-1728insGT
ENST00000686888.1:c.86-197_86-196insGT	ENSP00000509619.1:n.86-197_86-196insGT
ENST00000687699.1:c.210-197_210-196insGT	ENSP00000508878.1:n.210-197_210-196insGT
ENST00000687786.1:n.1222_1223insGT
ENST00000688588.1:c.86-197_86-196insGT	ENSP00000510802.1:n.86-197_86-196insGT
ENST00000688927.1:n.264-197_264-196insGT
ENST00000689283.1:c.210-1729_210-1728insGT	ENSP00000509050.1:n.210-1729_210-1728insGT
ENST00000689477.1:c.106_107insGT	ENSP00000508945.1:p.Glu36GlyfsTer?
ENST00000689765.1:c.86-1729_86-1728insGT	ENSP00000509625.1:n.86-1729_86-1728insGT
ENST00000690512.1:c.86-1238_86-1237insGT	ENSP00000509793.1:n.86-1238_86-1237insGT
ENST00000692039.1:c.86-111_86-110insGT	ENSP00000508821.1:n.86-111_86-110insGT
ENST00000692336.1:c.86-197_86-196insGT	ENSP00000508540.1:n.86-197_86-196insGT
ENST00000693133.1:n.226-1729_226-1728insGT
ENST00000263578.10:c.86-197_86-196insGT MANE Select	ENSP00000263578.5:n.86-197_86-196insGT
ENST00000263578.9:c.86-197_86-196insGT	ENSP00000263578.5:n.86-197_86-196insGT
ENST00000524751.5:n.223-1729_223-1728insGT
ENST00000525083.5:n.122-1729_122-1728insGT
ENST00000525770.5:c.86-1729_86-1728insGT	ENSP00000434739.1:n.86-1729_86-1728insGT
ENST00000526366.5:n.101-479_101-478insGT
ENST00000526525.1:n.246-1729_246-1728insGT
ENST00000527004.5:c.86-197_86-196insGT	ENSP00000436374.1:n.86-197_86-196insGT
ENST00000529802.1:n.136-197_136-196insGT
ENST00000532101.5:n.112_113insGT
ENST00000532125.1:c.44-197_44-196insGT	ENSP00000434178.1:n.44-197_44-196insGT
ENST00000533839.5:n.237+1949_237+1950insGT
ENST00000534011.5:n.158-1238_158-1237insGT
ENST00000534315.5:n.296_297insGT
NM_017547.3:c.86-197_86-196insGT	NP_060017.1:n.86-197_86-196insGT
NR_037647.1:n.253-1729_253-1728insGT
NR_037648.1:n.272-197_272-196insGT
XM_006718880.2:c.-650_-649insGT	XP_006718943.1:n.-650_-649insGT
XM_006718881.2:c.-232-1729_-232-1728insGT	XP_006718944.1:n.-232-1729_-232-1728insGT
XM_011542895.1:c.-622_-621insGT	XP_011541197.1:n.-622_-621insGT
XM_011542896.1:c.-445-197_-445-196insGT	XP_011541198.1:n.-445-197_-445-196insGT
XM_006718881.3:c.-232-1729_-232-1728insGT	XP_006718944.1:n.-232-1729_-232-1728insGT
XM_011542895.2:c.-622_-621insGT	XP_011541197.1:n.-622_-621insGT
XM_011542896.2:c.-445-197_-445-196insGT	XP_011541198.1:n.-445-197_-445-196insGT
XM_017018000.2:c.86-197_86-196insGT	XP_016873489.1:n.86-197_86-196insGT
XM_017018001.1:c.-445-197_-445-196insGT	XP_016873490.1:n.-445-197_-445-196insGT
XM_017018002.1:c.-224-1729_-224-1728insGT	XP_016873491.1:n.-224-1729_-224-1728insGT
XM_017018003.2:c.-453-197_-453-196insGT	XP_016873492.1:n.-453-197_-453-196insGT
XM_017018004.1:c.-650_-649insGT	XP_016873493.1:n.-650_-649insGT
XM_017018005.1:c.-848_-847insGT	XP_016873494.1:n.-848_-847insGT
XM_017018006.2:c.-453-197_-453-196insGT	XP_016873495.1:n.-453-197_-453-196insGT
NM_017547.4:c.86-197_86-196insGT MANE Select	NP_060017.1:n.86-197_86-196insGT
NR_037647.2:n.139-1729_139-1728insGT
NR_037648.2:n.263-197_263-196insGT