Canonical Allele Identifier: CA2007076789

Gene: FOXRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126271456_126271458delinsTGA , CM000673.2:g.126271456_126271458delinsTGA	GRCh38
NC_000011.9:g.126141351_126141353delinsTGA , CM000673.1:g.126141351_126141353delinsTGA	GRCh37
NC_000011.8:g.125646561_125646563delinsTGA	NCBI36
NG_028029.1:g.7417_7419delinsTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.283_285delinsTGA
ENST00000532101.6:n.282_284delinsTGA
ENST00000532125.2:c.105_107delinsTGA	ENSP00000434178.2:p.Ser35=
ENST00000533839.6:c.85+2165_85+2167delinsTGA	ENSP00000509952.1:n.85+2165_85+2167delinsTGA
ENST00000534011.6:n.381_383delinsTGA
ENST00000685484.1:c.105_107delinsTGA	ENSP00000510622.1:p.Ser35=
ENST00000685601.1:c.105_107delinsTGA	ENSP00000510603.1:p.Ser35=
ENST00000685765.1:c.105_107delinsTGA	ENSP00000509991.1:p.Ser35=
ENST00000685844.1:c.86-1513_86-1511delinsTGA	ENSP00000509820.1:n.86-1513_86-1511delinsTGA
ENST00000685857.1:n.283_285delinsTGA
ENST00000686242.1:c.86-1513_86-1511delinsTGA	ENSP00000508950.1:n.86-1513_86-1511delinsTGA
ENST00000686888.1:c.105_107delinsTGA	ENSP00000509619.1:p.Ser35=
ENST00000687699.1:c.229_231delinsTGA	ENSP00000508878.1:p.Ter77=
ENST00000687786.1:n.1438_1440delinsTGA
ENST00000688588.1:c.105_107delinsTGA	ENSP00000510802.1:p.Ser35=
ENST00000688927.1:n.283_285delinsTGA
ENST00000689283.1:c.210-1513_210-1511delinsTGA	ENSP00000509050.1:n.210-1513_210-1511delinsTGA
ENST00000689477.1:c.181_183delinsTGA	ENSP00000508945.1:p.Ter61=
ENST00000689765.1:c.86-1513_86-1511delinsTGA	ENSP00000509625.1:n.86-1513_86-1511delinsTGA
ENST00000690512.1:c.86-1022_86-1020delinsTGA	ENSP00000509793.1:n.86-1022_86-1020delinsTGA
ENST00000692039.1:c.191_193delinsTGA	ENSP00000508821.1:p.Leu64=
ENST00000692336.1:c.105_107delinsTGA	ENSP00000508540.1:p.Ser35=
ENST00000693133.1:n.226-1513_226-1511delinsTGA
ENST00000263578.10:c.105_107delinsTGA MANE Select	ENSP00000263578.5:p.Ser35=
ENST00000263578.9:c.105_107delinsTGA	ENSP00000263578.5:p.Ser35=
ENST00000524751.5:n.223-1513_223-1511delinsTGA
ENST00000525083.5:n.122-1513_122-1511delinsTGA
ENST00000525770.5:c.86-1513_86-1511delinsTGA	ENSP00000434739.1:n.86-1513_86-1511delinsTGA
ENST00000526366.5:n.101-263_101-261delinsTGA
ENST00000526525.1:n.246-1513_246-1511delinsTGA
ENST00000527004.5:c.105_107delinsTGA	ENSP00000436374.1:p.Ser35=
ENST00000529802.1:n.155_157delinsTGA
ENST00000532101.5:n.328_330delinsTGA
ENST00000532125.1:c.63_65delinsTGA	ENSP00000434178.1:p.Ser21=
ENST00000533839.5:n.237+2165_237+2167delinsTGA
ENST00000534011.5:n.158-1022_158-1020delinsTGA
ENST00000534315.5:n.512_514delinsTGA
NM_017547.3:c.105_107delinsTGA	NP_060017.1:p.Ser35=
NR_037647.1:n.253-1513_253-1511delinsTGA
NR_037648.1:n.291_293delinsTGA
XM_006718880.2:c.-434_-432delinsTGA	XP_006718943.1:n.-434_-432delinsTGA
XM_006718881.2:c.-232-1513_-232-1511delinsTGA	XP_006718944.1:n.-232-1513_-232-1511delinsTGA
XM_011542895.1:c.-406_-404delinsTGA	XP_011541197.1:n.-406_-404delinsTGA
XM_011542896.1:c.-426_-424delinsTGA	XP_011541198.1:n.-426_-424delinsTGA
XM_006718881.3:c.-232-1513_-232-1511delinsTGA	XP_006718944.1:n.-232-1513_-232-1511delinsTGA
XM_011542895.2:c.-406_-404delinsTGA	XP_011541197.1:n.-406_-404delinsTGA
XM_011542896.2:c.-426_-424delinsTGA	XP_011541198.1:n.-426_-424delinsTGA
XM_017018000.2:c.105_107delinsTGA	XP_016873489.1:p.Ser35=
XM_017018001.1:c.-426_-424delinsTGA	XP_016873490.1:n.-426_-424delinsTGA
XM_017018002.1:c.-224-1513_-224-1511delinsTGA	XP_016873491.1:n.-224-1513_-224-1511delinsTGA
XM_017018003.2:c.-434_-432delinsTGA	XP_016873492.1:n.-434_-432delinsTGA
XM_017018004.1:c.-434_-432delinsTGA	XP_016873493.1:n.-434_-432delinsTGA
XM_017018005.1:c.-632_-630delinsTGA	XP_016873494.1:n.-632_-630delinsTGA
XM_017018006.2:c.-434_-432delinsTGA	XP_016873495.1:n.-434_-432delinsTGA
NM_017547.4:c.105_107delinsTGA MANE Select	NP_060017.1:p.Ser35=
NR_037647.2:n.139-1513_139-1511delinsTGA
NR_037648.2:n.282_284delinsTGA