Canonical Allele Identifier: CA2007079555

Gene: FOXRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274995_126274999delinsCAGAG , CM000673.2:g.126274995_126274999delinsCAGAG	GRCh38
NC_000011.9:g.126144890_126144894delinsCAGAG , CM000673.1:g.126144890_126144894delinsCAGAG	GRCh37
NC_000011.8:g.125650100_125650104delinsCAGAG	NCBI36
NG_028029.1:g.10956_10960delinsCAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.783_787delinsCAGAG
ENST00000532101.6:n.734-332_734-328delinsCAGAG
ENST00000532125.2:c.602_606delinsCAGAG	ENSP00000434178.2:p.Thr201=
ENST00000533839.6:c.86-799_86-795delinsCAGAG	ENSP00000509952.1:n.86-799_86-795delinsCAGAG
ENST00000534011.6:n.897_901delinsCAGAG
ENST00000685484.1:c.605_609delinsCAGAG	ENSP00000510622.1:p.Thr202=
ENST00000685601.1:c.605_609delinsCAGAG	ENSP00000510603.1:p.Thr202=
ENST00000685765.1:c.605_609delinsCAGAG	ENSP00000509991.1:p.Thr202=
ENST00000685844.1:c.*169-332_*169-328delinsCAGAG	ENSP00000509820.1:n.*169-332_*169-328delinsCAGAG
ENST00000685857.1:n.1039_1043delinsCAGAG
ENST00000686242.1:c.404_408delinsCAGAG	ENSP00000508950.1:n.404_408delinsCAGAG
ENST00000686888.1:c.*172_*176delinsCAGAG	ENSP00000509619.1:n.*172_*176delinsCAGAG
ENST00000687699.1:c.729_733delinsCAGAG	ENSP00000508878.1:n.729_733delinsCAGAG
ENST00000687786.1:n.2068-332_2068-328delinsCAGAG
ENST00000688100.1:n.1526_1530delinsCAGAG
ENST00000688588.1:c.605_609delinsCAGAG	ENSP00000510802.1:p.Thr202=
ENST00000688927.1:n.2511_2515delinsCAGAG
ENST00000689283.1:c.*268_*272delinsCAGAG	ENSP00000509050.1:n.*268_*272delinsCAGAG
ENST00000689477.1:c.*498_*502delinsCAGAG	ENSP00000508945.1:n.*498_*502delinsCAGAG
ENST00000689765.1:c.*169-376_*169-372delinsCAGAG	ENSP00000509625.1:n.*169-376_*169-372delinsCAGAG
ENST00000690512.1:c.*456_*460delinsCAGAG	ENSP00000509793.1:n.*456_*460delinsCAGAG
ENST00000692039.1:c.*403_*407delinsCAGAG	ENSP00000508821.1:n.*403_*407delinsCAGAG
ENST00000692336.1:c.629_633delinsCAGAG	ENSP00000508540.1:p.Thr210=
ENST00000693133.1:n.780_784delinsCAGAG
ENST00000263578.10:c.605_609delinsCAGAG MANE Select	ENSP00000263578.5:p.Thr202=
ENST00000263578.9:c.605_609delinsCAGAG	ENSP00000263578.5:p.Thr202=
ENST00000524751.5:n.541_545delinsCAGAG
ENST00000525083.5:n.352-332_352-328delinsCAGAG
ENST00000525770.5:c.*237_*241delinsCAGAG	ENSP00000434739.1:n.*237_*241delinsCAGAG
ENST00000526366.5:n.536_540delinsCAGAG
ENST00000527004.5:c.534-332_534-328delinsCAGAG	ENSP00000436374.1:n.534-332_534-328delinsCAGAG
ENST00000527875.1:n.435_439delinsCAGAG
ENST00000530642.1:n.1082_1086delinsCAGAG
ENST00000532101.5:n.828_832delinsCAGAG
ENST00000532125.1:c.563_567delinsCAGAG	ENSP00000434178.1:p.Thr188=
ENST00000533395.5:n.365-332_365-328delinsCAGAG
ENST00000533839.5:n.238-799_238-795delinsCAGAG
ENST00000534011.5:n.657_661delinsCAGAG
ENST00000534315.5:n.944-332_944-328delinsCAGAG
NM_017547.3:c.605_609delinsCAGAG	NP_060017.1:p.Thr202=
NR_037647.1:n.551_555delinsCAGAG
NR_037648.1:n.791_795delinsCAGAG
XM_006718879.2:c.95_99delinsCAGAG	XP_006718942.1:p.Thr32=
XM_006718880.2:c.-2-332_-2-328delinsCAGAG	XP_006718943.1:n.-2-332_-2-328delinsCAGAG
XM_006718881.2:c.-2-332_-2-328delinsCAGAG	XP_006718944.1:n.-2-332_-2-328delinsCAGAG
XM_011542895.1:c.95_99delinsCAGAG	XP_011541197.1:p.Thr32=
XM_011542896.1:c.95_99delinsCAGAG	XP_011541198.1:p.Thr32=
XM_006718879.3:c.95_99delinsCAGAG	XP_006718942.1:p.Thr32=
XM_006718881.3:c.-2-332_-2-328delinsCAGAG	XP_006718944.1:n.-2-332_-2-328delinsCAGAG
XM_011542895.2:c.95_99delinsCAGAG	XP_011541197.1:p.Thr32=
XM_011542896.2:c.95_99delinsCAGAG	XP_011541198.1:p.Thr32=
XM_017018000.2:c.605_609delinsCAGAG	XP_016873489.1:p.Thr202=
XM_017018001.1:c.95_99delinsCAGAG	XP_016873490.1:p.Thr32=
XM_017018002.1:c.95_99delinsCAGAG	XP_016873491.1:p.Thr32=
XM_017018003.2:c.-2-332_-2-328delinsCAGAG	XP_016873492.1:n.-2-332_-2-328delinsCAGAG
XM_017018004.1:c.-2-332_-2-328delinsCAGAG	XP_016873493.1:n.-2-332_-2-328delinsCAGAG
XM_017018005.1:c.-2-332_-2-328delinsCAGAG	XP_016873494.1:n.-2-332_-2-328delinsCAGAG
XM_017018006.2:c.-2-332_-2-328delinsCAGAG	XP_016873495.1:n.-2-332_-2-328delinsCAGAG
NM_017547.4:c.605_609delinsCAGAG MANE Select	NP_060017.1:p.Thr202=
NR_037647.2:n.437_441delinsCAGAG
NR_037648.2:n.782_786delinsCAGAG