Canonical Allele Identifier: CA2575022734

Gene: FOXRED1

Linked Data

• gnomAD v4: 11-126275026-GGCTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275033_126275036del , CM000673.2:g.126275033_126275036del	GRCh38
NC_000011.9:g.126144928_126144931del , CM000673.1:g.126144928_126144931del	GRCh37
NC_000011.8:g.125650138_125650141del	NCBI36
NG_028029.1:g.10994_10997del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.821_824del
ENST00000532101.6:n.734-294_734-291del
ENST00000532125.2:c.628+12_628+15del	ENSP00000434178.2:n.628+12_628+15del
ENST00000533839.6:c.86-761_86-758del	ENSP00000509952.1:n.86-761_86-758del
ENST00000534011.6:n.923+12_923+15del
ENST00000685484.1:c.631+12_631+15del	ENSP00000510622.1:n.631+12_631+15del
ENST00000685601.1:c.631+12_631+15del	ENSP00000510603.1:n.631+12_631+15del
ENST00000685765.1:c.631+12_631+15del	ENSP00000509991.1:n.631+12_631+15del
ENST00000685844.1:c.*169-294_*169-291del	ENSP00000509820.1:n.*169-294_*169-291del
ENST00000685857.1:n.1077_1080del
ENST00000686242.1:c.430+12_430+15del	ENSP00000508950.1:n.430+12_430+15del
ENST00000686888.1:c.*198+12_*198+15del	ENSP00000509619.1:n.*198+12_*198+15del
ENST00000687699.1:c.755+12_755+15del	ENSP00000508878.1:n.755+12_755+15del
ENST00000687786.1:n.2068-294_2068-291del
ENST00000688100.1:n.1552+12_1552+15del
ENST00000688588.1:c.631+12_631+15del	ENSP00000510802.1:n.631+12_631+15del
ENST00000688927.1:n.2549_2552del
ENST00000689283.1:c.*294+12_*294+15del	ENSP00000509050.1:n.*294+12_*294+15del
ENST00000689477.1:c.*524+12_*524+15del	ENSP00000508945.1:n.*524+12_*524+15del
ENST00000689765.1:c.*169-338_*169-335del	ENSP00000509625.1:n.*169-338_*169-335del
ENST00000690512.1:c.*482+12_*482+15del	ENSP00000509793.1:n.*482+12_*482+15del
ENST00000692039.1:c.*429+12_*429+15del	ENSP00000508821.1:n.*429+12_*429+15del
ENST00000692336.1:c.655+12_655+15del	ENSP00000508540.1:n.655+12_655+15del
ENST00000693133.1:n.818_821del
ENST00000263578.10:c.631+12_631+15del MANE Select	ENSP00000263578.5:n.631+12_631+15del
ENST00000263578.9:c.631+12_631+15del	ENSP00000263578.5:n.631+12_631+15del
ENST00000524751.5:n.579_582del
ENST00000525083.5:n.352-294_352-291del
ENST00000525770.5:c.*263+12_*263+15del	ENSP00000434739.1:n.*263+12_*263+15del
ENST00000527004.5:c.534-294_534-291del	ENSP00000436374.1:n.534-294_534-291del
ENST00000527875.1:n.473_476del
ENST00000530642.1:n.1120_1123del
ENST00000532101.5:n.854+12_854+15del
ENST00000532125.1:c.589+12_589+15del	ENSP00000434178.1:n.589+12_589+15del
ENST00000533395.5:n.365-294_365-291del
ENST00000533839.5:n.238-761_238-758del
ENST00000534011.5:n.683+12_683+15del
ENST00000534315.5:n.944-294_944-291del
NM_017547.3:c.631+12_631+15del	NP_060017.1:n.631+12_631+15del
NR_037647.1:n.577+12_577+15del
NR_037648.1:n.817+12_817+15del
XM_006718879.2:c.121+12_121+15del	XP_006718942.1:n.121+12_121+15del
XM_006718880.2:c.-2-294_-2-291del	XP_006718943.1:n.-2-294_-2-291del
XM_006718881.2:c.-2-294_-2-291del	XP_006718944.1:n.-2-294_-2-291del
XM_011542895.1:c.121+12_121+15del	XP_011541197.1:n.121+12_121+15del
XM_011542896.1:c.121+12_121+15del	XP_011541198.1:n.121+12_121+15del
XM_006718879.3:c.121+12_121+15del	XP_006718942.1:n.121+12_121+15del
XM_006718881.3:c.-2-294_-2-291del	XP_006718944.1:n.-2-294_-2-291del
XM_011542895.2:c.121+12_121+15del	XP_011541197.1:n.121+12_121+15del
XM_011542896.2:c.121+12_121+15del	XP_011541198.1:n.121+12_121+15del
XM_017018000.2:c.631+12_631+15del	XP_016873489.1:n.631+12_631+15del
XM_017018001.1:c.121+12_121+15del	XP_016873490.1:n.121+12_121+15del
XM_017018002.1:c.121+12_121+15del	XP_016873491.1:n.121+12_121+15del
XM_017018003.2:c.-2-294_-2-291del	XP_016873492.1:n.-2-294_-2-291del
XM_017018004.1:c.-2-294_-2-291del	XP_016873493.1:n.-2-294_-2-291del
XM_017018005.1:c.-2-294_-2-291del	XP_016873494.1:n.-2-294_-2-291del
XM_017018006.2:c.-2-294_-2-291del	XP_016873495.1:n.-2-294_-2-291del
NM_017547.4:c.631+12_631+15del MANE Select	NP_060017.1:n.631+12_631+15del
NR_037647.2:n.463+12_463+15del
NR_037648.2:n.808+12_808+15del