Canonical Allele Identifier: CA2616727323

Gene: FOXRED1

Linked Data

• gnomAD v4: 11-126271238-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126271238_126271239insC , CM000673.2:g.126271238_126271239insC	GRCh38
NC_000011.9:g.126141133_126141134insC , CM000673.1:g.126141133_126141134insC	GRCh37
NC_000011.8:g.125646343_125646344insC	NCBI36
NG_028029.1:g.7199_7200insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.264-199_264-198insC
ENST00000532101.6:n.64_65insC
ENST00000532125.2:c.86-199_86-198insC	ENSP00000434178.2:n.86-199_86-198insC
ENST00000533839.6:c.85+1947_85+1948insC	ENSP00000509952.1:n.85+1947_85+1948insC
ENST00000534011.6:n.163_164insC
ENST00000685484.1:c.86-199_86-198insC	ENSP00000510622.1:n.86-199_86-198insC
ENST00000685601.1:c.86-199_86-198insC	ENSP00000510603.1:n.86-199_86-198insC
ENST00000685765.1:c.86-199_86-198insC	ENSP00000509991.1:n.86-199_86-198insC
ENST00000685844.1:c.86-1731_86-1730insC	ENSP00000509820.1:n.86-1731_86-1730insC
ENST00000685857.1:n.264-199_264-198insC
ENST00000686242.1:c.86-1731_86-1730insC	ENSP00000508950.1:n.86-1731_86-1730insC
ENST00000686888.1:c.86-199_86-198insC	ENSP00000509619.1:n.86-199_86-198insC
ENST00000687699.1:c.210-199_210-198insC	ENSP00000508878.1:n.210-199_210-198insC
ENST00000687786.1:n.1220_1221insC
ENST00000688588.1:c.86-199_86-198insC	ENSP00000510802.1:n.86-199_86-198insC
ENST00000688927.1:n.264-199_264-198insC
ENST00000689283.1:c.210-1731_210-1730insC	ENSP00000509050.1:n.210-1731_210-1730insC
ENST00000689477.1:c.104_105insC	ENSP00000508945.1:p.Glu35AspfsTer4
ENST00000689765.1:c.86-1731_86-1730insC	ENSP00000509625.1:n.86-1731_86-1730insC
ENST00000690512.1:c.86-1240_86-1239insC	ENSP00000509793.1:n.86-1240_86-1239insC
ENST00000692039.1:c.86-113_86-112insC	ENSP00000508821.1:n.86-113_86-112insC
ENST00000692336.1:c.86-199_86-198insC	ENSP00000508540.1:n.86-199_86-198insC
ENST00000693133.1:n.226-1731_226-1730insC
ENST00000263578.10:c.86-199_86-198insC MANE Select	ENSP00000263578.5:n.86-199_86-198insC
ENST00000263578.9:c.86-199_86-198insC	ENSP00000263578.5:n.86-199_86-198insC
ENST00000524751.5:n.223-1731_223-1730insC
ENST00000525083.5:n.122-1731_122-1730insC
ENST00000525770.5:c.86-1731_86-1730insC	ENSP00000434739.1:n.86-1731_86-1730insC
ENST00000526366.5:n.101-481_101-480insC
ENST00000526525.1:n.246-1731_246-1730insC
ENST00000527004.5:c.86-199_86-198insC	ENSP00000436374.1:n.86-199_86-198insC
ENST00000529802.1:n.136-199_136-198insC
ENST00000532101.5:n.110_111insC
ENST00000532125.1:c.44-199_44-198insC	ENSP00000434178.1:n.44-199_44-198insC
ENST00000533839.5:n.237+1947_237+1948insC
ENST00000534011.5:n.158-1240_158-1239insC
ENST00000534315.5:n.294_295insC
NM_017547.3:c.86-199_86-198insC	NP_060017.1:n.86-199_86-198insC
NR_037647.1:n.253-1731_253-1730insC
NR_037648.1:n.272-199_272-198insC
XM_006718880.2:c.-652_-651insC	XP_006718943.1:n.-652_-651insC
XM_006718881.2:c.-232-1731_-232-1730insC	XP_006718944.1:n.-232-1731_-232-1730insC
XM_011542895.1:c.-624_-623insC	XP_011541197.1:n.-624_-623insC
XM_011542896.1:c.-445-199_-445-198insC	XP_011541198.1:n.-445-199_-445-198insC
XM_006718881.3:c.-232-1731_-232-1730insC	XP_006718944.1:n.-232-1731_-232-1730insC
XM_011542895.2:c.-624_-623insC	XP_011541197.1:n.-624_-623insC
XM_011542896.2:c.-445-199_-445-198insC	XP_011541198.1:n.-445-199_-445-198insC
XM_017018000.2:c.86-199_86-198insC	XP_016873489.1:n.86-199_86-198insC
XM_017018001.1:c.-445-199_-445-198insC	XP_016873490.1:n.-445-199_-445-198insC
XM_017018002.1:c.-224-1731_-224-1730insC	XP_016873491.1:n.-224-1731_-224-1730insC
XM_017018003.2:c.-453-199_-453-198insC	XP_016873492.1:n.-453-199_-453-198insC
XM_017018004.1:c.-652_-651insC	XP_016873493.1:n.-652_-651insC
XM_017018005.1:c.-850_-849insC	XP_016873494.1:n.-850_-849insC
XM_017018006.2:c.-453-199_-453-198insC	XP_016873495.1:n.-453-199_-453-198insC
NM_017547.4:c.86-199_86-198insC MANE Select	NP_060017.1:n.86-199_86-198insC
NR_037647.2:n.139-1731_139-1730insC
NR_037648.2:n.263-199_263-198insC