Canonical Allele Identifier: CA2520616474

Gene: FOXRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126271614_126271615insTG , CM000673.2:g.126271614_126271615insTG	GRCh38
NC_000011.9:g.126141509_126141510insTG , CM000673.1:g.126141509_126141510insTG	GRCh37
NC_000011.8:g.125646719_125646720insTG	NCBI36
NG_028029.1:g.7575_7576insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.441_442insTG
ENST00000532101.6:n.440_441insTG
ENST00000532125.2:c.263_264insTG	ENSP00000434178.2:p.Arg88SerfsTer9
ENST00000533839.6:c.85+2323_85+2324insTG	ENSP00000509952.1:n.85+2323_85+2324insTG
ENST00000534011.6:n.539_540insTG
ENST00000685484.1:c.263_264insTG	ENSP00000510622.1:p.Arg88SerfsTer9
ENST00000685601.1:c.263_264insTG	ENSP00000510603.1:p.Arg88SerfsTer9
ENST00000685765.1:c.263_264insTG	ENSP00000509991.1:p.Arg88SerfsTer9
ENST00000685844.1:c.86-1355_86-1354insTG	ENSP00000509820.1:n.86-1355_86-1354insTG
ENST00000685857.1:n.441_442insTG
ENST00000686242.1:c.86-1355_86-1354insTG	ENSP00000508950.1:n.86-1355_86-1354insTG
ENST00000686888.1:c.263_264insTG	ENSP00000509619.1:p.Arg88SerfsTer9
ENST00000687699.1:c.387_388insTG	ENSP00000508878.1:n.387_388insTG
ENST00000687786.1:n.1596_1597insTG
ENST00000688588.1:c.263_264insTG	ENSP00000510802.1:p.Arg88SerfsTer9
ENST00000688927.1:n.441_442insTG
ENST00000689283.1:c.210-1355_210-1354insTG	ENSP00000509050.1:n.210-1355_210-1354insTG
ENST00000689477.1:c.*156_*157insTG	ENSP00000508945.1:n.*156_*157insTG
ENST00000689765.1:c.86-1355_86-1354insTG	ENSP00000509625.1:n.86-1355_86-1354insTG
ENST00000690512.1:c.86-864_86-863insTG	ENSP00000509793.1:n.86-864_86-863insTG
ENST00000692039.1:c.*61_*62insTG	ENSP00000508821.1:n.*61_*62insTG
ENST00000692336.1:c.263_264insTG	ENSP00000508540.1:p.Arg88SerfsTer9
ENST00000693133.1:n.226-1355_226-1354insTG
ENST00000263578.10:c.263_264insTG MANE Select	ENSP00000263578.5:p.Arg88SerfsTer9
ENST00000263578.9:c.263_264insTG	ENSP00000263578.5:p.Arg88SerfsTer9
ENST00000524751.5:n.223-1355_223-1354insTG
ENST00000525083.5:n.122-1355_122-1354insTG
ENST00000525770.5:c.86-1355_86-1354insTG	ENSP00000434739.1:n.86-1355_86-1354insTG
ENST00000526366.5:n.101-105_101-104insTG
ENST00000526525.1:n.246-1355_246-1354insTG
ENST00000527004.5:c.263_264insTG	ENSP00000436374.1:p.Arg88SerfsTer9
ENST00000529802.1:n.313_314insTG
ENST00000532101.5:n.486_487insTG
ENST00000532125.1:c.221_222insTG	ENSP00000434178.1:p.Arg74SerfsTer9
ENST00000533839.5:n.237+2323_237+2324insTG
ENST00000534011.5:n.158-864_158-863insTG
ENST00000534315.5:n.670_671insTG
NM_017547.3:c.263_264insTG	NP_060017.1:p.Arg88SerfsTer9
NR_037647.1:n.253-1355_253-1354insTG
NR_037648.1:n.449_450insTG
XM_006718880.2:c.-276_-275insTG	XP_006718943.1:n.-276_-275insTG
XM_006718881.2:c.-232-1355_-232-1354insTG	XP_006718944.1:n.-232-1355_-232-1354insTG
XM_011542895.1:c.-248_-247insTG	XP_011541197.1:n.-248_-247insTG
XM_011542896.1:c.-268_-267insTG	XP_011541198.1:n.-268_-267insTG
XM_006718881.3:c.-232-1355_-232-1354insTG	XP_006718944.1:n.-232-1355_-232-1354insTG
XM_011542895.2:c.-248_-247insTG	XP_011541197.1:n.-248_-247insTG
XM_011542896.2:c.-268_-267insTG	XP_011541198.1:n.-268_-267insTG
XM_017018000.2:c.263_264insTG	XP_016873489.1:p.Arg88SerfsTer9
XM_017018001.1:c.-268_-267insTG	XP_016873490.1:n.-268_-267insTG
XM_017018002.1:c.-224-1355_-224-1354insTG	XP_016873491.1:n.-224-1355_-224-1354insTG
XM_017018003.2:c.-276_-275insTG	XP_016873492.1:n.-276_-275insTG
XM_017018004.1:c.-276_-275insTG	XP_016873493.1:n.-276_-275insTG
XM_017018005.1:c.-474_-473insTG	XP_016873494.1:n.-474_-473insTG
XM_017018006.2:c.-276_-275insTG	XP_016873495.1:n.-276_-275insTG
NM_017547.4:c.263_264insTG MANE Select	NP_060017.1:p.Arg88SerfsTer9
NR_037647.2:n.139-1355_139-1354insTG
NR_037648.2:n.440_441insTG