Canonical Allele Identifier: CA2007076605

Gene: FOXRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126271271_126271273delinsCTG , CM000673.2:g.126271271_126271273delinsCTG	GRCh38
NC_000011.9:g.126141166_126141168delinsCTG , CM000673.1:g.126141166_126141168delinsCTG	GRCh37
NC_000011.8:g.125646376_125646378delinsCTG	NCBI36
NG_028029.1:g.7232_7234delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.264-166_264-164delinsCTG
ENST00000532101.6:n.97_99delinsCTG
ENST00000532125.2:c.86-166_86-164delinsCTG	ENSP00000434178.2:n.86-166_86-164delinsCTG
ENST00000533839.6:c.85+1980_85+1982delinsCTG	ENSP00000509952.1:n.85+1980_85+1982delinsCTG
ENST00000534011.6:n.196_198delinsCTG
ENST00000685484.1:c.86-166_86-164delinsCTG	ENSP00000510622.1:n.86-166_86-164delinsCTG
ENST00000685601.1:c.86-166_86-164delinsCTG	ENSP00000510603.1:n.86-166_86-164delinsCTG
ENST00000685765.1:c.86-166_86-164delinsCTG	ENSP00000509991.1:n.86-166_86-164delinsCTG
ENST00000685844.1:c.86-1698_86-1696delinsCTG	ENSP00000509820.1:n.86-1698_86-1696delinsCTG
ENST00000685857.1:n.264-166_264-164delinsCTG
ENST00000686242.1:c.86-1698_86-1696delinsCTG	ENSP00000508950.1:n.86-1698_86-1696delinsCTG
ENST00000686888.1:c.86-166_86-164delinsCTG	ENSP00000509619.1:n.86-166_86-164delinsCTG
ENST00000687699.1:c.210-166_210-164delinsCTG	ENSP00000508878.1:n.210-166_210-164delinsCTG
ENST00000687786.1:n.1253_1255delinsCTG
ENST00000688588.1:c.86-166_86-164delinsCTG	ENSP00000510802.1:n.86-166_86-164delinsCTG
ENST00000688927.1:n.264-166_264-164delinsCTG
ENST00000689283.1:c.210-1698_210-1696delinsCTG	ENSP00000509050.1:n.210-1698_210-1696delinsCTG
ENST00000689477.1:c.137_139delinsCTG	ENSP00000508945.1:p.Thr46=
ENST00000689765.1:c.86-1698_86-1696delinsCTG	ENSP00000509625.1:n.86-1698_86-1696delinsCTG
ENST00000690512.1:c.86-1207_86-1205delinsCTG	ENSP00000509793.1:n.86-1207_86-1205delinsCTG
ENST00000692039.1:c.86-80_86-78delinsCTG	ENSP00000508821.1:n.86-80_86-78delinsCTG
ENST00000692336.1:c.86-166_86-164delinsCTG	ENSP00000508540.1:n.86-166_86-164delinsCTG
ENST00000693133.1:n.226-1698_226-1696delinsCTG
ENST00000263578.10:c.86-166_86-164delinsCTG MANE Select	ENSP00000263578.5:n.86-166_86-164delinsCTG
ENST00000263578.9:c.86-166_86-164delinsCTG	ENSP00000263578.5:n.86-166_86-164delinsCTG
ENST00000524751.5:n.223-1698_223-1696delinsCTG
ENST00000525083.5:n.122-1698_122-1696delinsCTG
ENST00000525770.5:c.86-1698_86-1696delinsCTG	ENSP00000434739.1:n.86-1698_86-1696delinsCTG
ENST00000526366.5:n.101-448_101-446delinsCTG
ENST00000526525.1:n.246-1698_246-1696delinsCTG
ENST00000527004.5:c.86-166_86-164delinsCTG	ENSP00000436374.1:n.86-166_86-164delinsCTG
ENST00000529802.1:n.136-166_136-164delinsCTG
ENST00000532101.5:n.143_145delinsCTG
ENST00000532125.1:c.44-166_44-164delinsCTG	ENSP00000434178.1:n.44-166_44-164delinsCTG
ENST00000533839.5:n.237+1980_237+1982delinsCTG
ENST00000534011.5:n.158-1207_158-1205delinsCTG
ENST00000534315.5:n.327_329delinsCTG
NM_017547.3:c.86-166_86-164delinsCTG	NP_060017.1:n.86-166_86-164delinsCTG
NR_037647.1:n.253-1698_253-1696delinsCTG
NR_037648.1:n.272-166_272-164delinsCTG
XM_006718880.2:c.-619_-617delinsCTG	XP_006718943.1:n.-619_-617delinsCTG
XM_006718881.2:c.-232-1698_-232-1696delinsCTG	XP_006718944.1:n.-232-1698_-232-1696delinsCTG
XM_011542895.1:c.-591_-589delinsCTG	XP_011541197.1:n.-591_-589delinsCTG
XM_011542896.1:c.-445-166_-445-164delinsCTG	XP_011541198.1:n.-445-166_-445-164delinsCTG
XM_006718881.3:c.-232-1698_-232-1696delinsCTG	XP_006718944.1:n.-232-1698_-232-1696delinsCTG
XM_011542895.2:c.-591_-589delinsCTG	XP_011541197.1:n.-591_-589delinsCTG
XM_011542896.2:c.-445-166_-445-164delinsCTG	XP_011541198.1:n.-445-166_-445-164delinsCTG
XM_017018000.2:c.86-166_86-164delinsCTG	XP_016873489.1:n.86-166_86-164delinsCTG
XM_017018001.1:c.-445-166_-445-164delinsCTG	XP_016873490.1:n.-445-166_-445-164delinsCTG
XM_017018002.1:c.-224-1698_-224-1696delinsCTG	XP_016873491.1:n.-224-1698_-224-1696delinsCTG
XM_017018003.2:c.-453-166_-453-164delinsCTG	XP_016873492.1:n.-453-166_-453-164delinsCTG
XM_017018004.1:c.-619_-617delinsCTG	XP_016873493.1:n.-619_-617delinsCTG
XM_017018005.1:c.-817_-815delinsCTG	XP_016873494.1:n.-817_-815delinsCTG
XM_017018006.2:c.-453-166_-453-164delinsCTG	XP_016873495.1:n.-453-166_-453-164delinsCTG
NM_017547.4:c.86-166_86-164delinsCTG MANE Select	NP_060017.1:n.86-166_86-164delinsCTG
NR_037647.2:n.139-1698_139-1696delinsCTG
NR_037648.2:n.263-166_263-164delinsCTG