Canonical Allele Identifier: CA2007079554

Gene: FOXRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274995_126274997delinsCAG , CM000673.2:g.126274995_126274997delinsCAG	GRCh38
NC_000011.9:g.126144890_126144892delinsCAG , CM000673.1:g.126144890_126144892delinsCAG	GRCh37
NC_000011.8:g.125650100_125650102delinsCAG	NCBI36
NG_028029.1:g.10956_10958delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.783_785delinsCAG
ENST00000532101.6:n.734-332_734-330delinsCAG
ENST00000532125.2:c.602_604delinsCAG	ENSP00000434178.2:p.Thr201=
ENST00000533839.6:c.86-799_86-797delinsCAG	ENSP00000509952.1:n.86-799_86-797delinsCAG
ENST00000534011.6:n.897_899delinsCAG
ENST00000685484.1:c.605_607delinsCAG	ENSP00000510622.1:p.Thr202=
ENST00000685601.1:c.605_607delinsCAG	ENSP00000510603.1:p.Thr202=
ENST00000685765.1:c.605_607delinsCAG	ENSP00000509991.1:p.Thr202=
ENST00000685844.1:c.*169-332_*169-330delinsCAG	ENSP00000509820.1:n.*169-332_*169-330delinsCAG
ENST00000685857.1:n.1039_1041delinsCAG
ENST00000686242.1:c.404_406delinsCAG	ENSP00000508950.1:n.404_406delinsCAG
ENST00000686888.1:c.*172_*174delinsCAG	ENSP00000509619.1:n.*172_*174delinsCAG
ENST00000687699.1:c.729_731delinsCAG	ENSP00000508878.1:n.729_731delinsCAG
ENST00000687786.1:n.2068-332_2068-330delinsCAG
ENST00000688100.1:n.1526_1528delinsCAG
ENST00000688588.1:c.605_607delinsCAG	ENSP00000510802.1:p.Thr202=
ENST00000688927.1:n.2511_2513delinsCAG
ENST00000689283.1:c.*268_*270delinsCAG	ENSP00000509050.1:n.*268_*270delinsCAG
ENST00000689477.1:c.*498_*500delinsCAG	ENSP00000508945.1:n.*498_*500delinsCAG
ENST00000689765.1:c.*169-376_*169-374delinsCAG	ENSP00000509625.1:n.*169-376_*169-374delinsCAG
ENST00000690512.1:c.*456_*458delinsCAG	ENSP00000509793.1:n.*456_*458delinsCAG
ENST00000692039.1:c.*403_*405delinsCAG	ENSP00000508821.1:n.*403_*405delinsCAG
ENST00000692336.1:c.629_631delinsCAG	ENSP00000508540.1:p.Thr210=
ENST00000693133.1:n.780_782delinsCAG
ENST00000263578.10:c.605_607delinsCAG MANE Select	ENSP00000263578.5:p.Thr202=
ENST00000263578.9:c.605_607delinsCAG	ENSP00000263578.5:p.Thr202=
ENST00000524751.5:n.541_543delinsCAG
ENST00000525083.5:n.352-332_352-330delinsCAG
ENST00000525770.5:c.*237_*239delinsCAG	ENSP00000434739.1:n.*237_*239delinsCAG
ENST00000526366.5:n.536_538delinsCAG
ENST00000527004.5:c.534-332_534-330delinsCAG	ENSP00000436374.1:n.534-332_534-330delinsCAG
ENST00000527875.1:n.435_437delinsCAG
ENST00000530642.1:n.1082_1084delinsCAG
ENST00000532101.5:n.828_830delinsCAG
ENST00000532125.1:c.563_565delinsCAG	ENSP00000434178.1:p.Thr188=
ENST00000533395.5:n.365-332_365-330delinsCAG
ENST00000533839.5:n.238-799_238-797delinsCAG
ENST00000534011.5:n.657_659delinsCAG
ENST00000534315.5:n.944-332_944-330delinsCAG
NM_017547.3:c.605_607delinsCAG	NP_060017.1:p.Thr202=
NR_037647.1:n.551_553delinsCAG
NR_037648.1:n.791_793delinsCAG
XM_006718879.2:c.95_97delinsCAG	XP_006718942.1:p.Thr32=
XM_006718880.2:c.-2-332_-2-330delinsCAG	XP_006718943.1:n.-2-332_-2-330delinsCAG
XM_006718881.2:c.-2-332_-2-330delinsCAG	XP_006718944.1:n.-2-332_-2-330delinsCAG
XM_011542895.1:c.95_97delinsCAG	XP_011541197.1:p.Thr32=
XM_011542896.1:c.95_97delinsCAG	XP_011541198.1:p.Thr32=
XM_006718879.3:c.95_97delinsCAG	XP_006718942.1:p.Thr32=
XM_006718881.3:c.-2-332_-2-330delinsCAG	XP_006718944.1:n.-2-332_-2-330delinsCAG
XM_011542895.2:c.95_97delinsCAG	XP_011541197.1:p.Thr32=
XM_011542896.2:c.95_97delinsCAG	XP_011541198.1:p.Thr32=
XM_017018000.2:c.605_607delinsCAG	XP_016873489.1:p.Thr202=
XM_017018001.1:c.95_97delinsCAG	XP_016873490.1:p.Thr32=
XM_017018002.1:c.95_97delinsCAG	XP_016873491.1:p.Thr32=
XM_017018003.2:c.-2-332_-2-330delinsCAG	XP_016873492.1:n.-2-332_-2-330delinsCAG
XM_017018004.1:c.-2-332_-2-330delinsCAG	XP_016873493.1:n.-2-332_-2-330delinsCAG
XM_017018005.1:c.-2-332_-2-330delinsCAG	XP_016873494.1:n.-2-332_-2-330delinsCAG
XM_017018006.2:c.-2-332_-2-330delinsCAG	XP_016873495.1:n.-2-332_-2-330delinsCAG
NM_017547.4:c.605_607delinsCAG MANE Select	NP_060017.1:p.Thr202=
NR_037647.2:n.437_439delinsCAG
NR_037648.2:n.782_784delinsCAG