Canonical Allele Identifier: CA2616727390

Gene: FOXRED1

Linked Data

• gnomAD v4: 11-126271242-GACTGAT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126271243_126271248del , CM000673.2:g.126271243_126271248del	GRCh38
NC_000011.9:g.126141138_126141143del , CM000673.1:g.126141138_126141143del	GRCh37
NC_000011.8:g.125646348_125646353del	NCBI36
NG_028029.1:g.7204_7209del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.264-194_264-189del
ENST00000532101.6:n.69_74del
ENST00000532125.2:c.86-194_86-189del	ENSP00000434178.2:n.86-194_86-189del
ENST00000533839.6:c.85+1952_85+1957del	ENSP00000509952.1:n.85+1952_85+1957del
ENST00000534011.6:n.168_173del
ENST00000685484.1:c.86-194_86-189del	ENSP00000510622.1:n.86-194_86-189del
ENST00000685601.1:c.86-194_86-189del	ENSP00000510603.1:n.86-194_86-189del
ENST00000685765.1:c.86-194_86-189del	ENSP00000509991.1:n.86-194_86-189del
ENST00000685844.1:c.86-1726_86-1721del	ENSP00000509820.1:n.86-1726_86-1721del
ENST00000685857.1:n.264-194_264-189del
ENST00000686242.1:c.86-1726_86-1721del	ENSP00000508950.1:n.86-1726_86-1721del
ENST00000686888.1:c.86-194_86-189del	ENSP00000509619.1:n.86-194_86-189del
ENST00000687699.1:c.210-194_210-189del	ENSP00000508878.1:n.210-194_210-189del
ENST00000687786.1:n.1225_1230del
ENST00000688588.1:c.86-194_86-189del	ENSP00000510802.1:n.86-194_86-189del
ENST00000688927.1:n.264-194_264-189del
ENST00000689283.1:c.210-1726_210-1721del	ENSP00000509050.1:n.210-1726_210-1721del
ENST00000689477.1:c.109_114del	ENSP00000508945.1:p.Thr37_Asp38del
ENST00000689765.1:c.86-1726_86-1721del	ENSP00000509625.1:n.86-1726_86-1721del
ENST00000690512.1:c.86-1235_86-1230del	ENSP00000509793.1:n.86-1235_86-1230del
ENST00000692039.1:c.86-108_86-103del	ENSP00000508821.1:n.86-108_86-103del
ENST00000692336.1:c.86-194_86-189del	ENSP00000508540.1:n.86-194_86-189del
ENST00000693133.1:n.226-1726_226-1721del
ENST00000263578.10:c.86-194_86-189del MANE Select	ENSP00000263578.5:n.86-194_86-189del
ENST00000263578.9:c.86-194_86-189del	ENSP00000263578.5:n.86-194_86-189del
ENST00000524751.5:n.223-1726_223-1721del
ENST00000525083.5:n.122-1726_122-1721del
ENST00000525770.5:c.86-1726_86-1721del	ENSP00000434739.1:n.86-1726_86-1721del
ENST00000526366.5:n.101-476_101-471del
ENST00000526525.1:n.246-1726_246-1721del
ENST00000527004.5:c.86-194_86-189del	ENSP00000436374.1:n.86-194_86-189del
ENST00000529802.1:n.136-194_136-189del
ENST00000532101.5:n.115_120del
ENST00000532125.1:c.44-194_44-189del	ENSP00000434178.1:n.44-194_44-189del
ENST00000533839.5:n.237+1952_237+1957del
ENST00000534011.5:n.158-1235_158-1230del
ENST00000534315.5:n.299_304del
NM_017547.3:c.86-194_86-189del	NP_060017.1:n.86-194_86-189del
NR_037647.1:n.253-1726_253-1721del
NR_037648.1:n.272-194_272-189del
XM_006718880.2:c.-647_-642del	XP_006718943.1:n.-647_-642del
XM_006718881.2:c.-232-1726_-232-1721del	XP_006718944.1:n.-232-1726_-232-1721del
XM_011542895.1:c.-619_-614del	XP_011541197.1:n.-619_-614del
XM_011542896.1:c.-445-194_-445-189del	XP_011541198.1:n.-445-194_-445-189del
XM_006718881.3:c.-232-1726_-232-1721del	XP_006718944.1:n.-232-1726_-232-1721del
XM_011542895.2:c.-619_-614del	XP_011541197.1:n.-619_-614del
XM_011542896.2:c.-445-194_-445-189del	XP_011541198.1:n.-445-194_-445-189del
XM_017018000.2:c.86-194_86-189del	XP_016873489.1:n.86-194_86-189del
XM_017018001.1:c.-445-194_-445-189del	XP_016873490.1:n.-445-194_-445-189del
XM_017018002.1:c.-224-1726_-224-1721del	XP_016873491.1:n.-224-1726_-224-1721del
XM_017018003.2:c.-453-194_-453-189del	XP_016873492.1:n.-453-194_-453-189del
XM_017018004.1:c.-647_-642del	XP_016873493.1:n.-647_-642del
XM_017018005.1:c.-845_-840del	XP_016873494.1:n.-845_-840del
XM_017018006.2:c.-453-194_-453-189del	XP_016873495.1:n.-453-194_-453-189del
NM_017547.4:c.86-194_86-189del MANE Select	NP_060017.1:n.86-194_86-189del
NR_037647.2:n.139-1726_139-1721del
NR_037648.2:n.263-194_263-189del