Canonical Allele Identifier: CA2007076486

Gene: FOXRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126271154G= , CM000673.2:g.126271154G=	GRCh38
NC_000011.9:g.126141049G= , CM000673.1:g.126141049G=	GRCh37
NC_000011.8:g.125646259G=	NCBI36
NG_028029.1:g.7115G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.264-283G=
ENST00000532101.6:n.46-66G=
ENST00000532125.2:c.86-283G=	ENSP00000434178.2:n.86-283G=
ENST00000533839.6:c.85+1863G=	ENSP00000509952.1:n.85+1863G=
ENST00000534011.6:n.145-66G=
ENST00000685484.1:c.86-283G=	ENSP00000510622.1:n.86-283G=
ENST00000685601.1:c.86-283G=	ENSP00000510603.1:n.86-283G=
ENST00000685765.1:c.86-283G=	ENSP00000509991.1:n.86-283G=
ENST00000685844.1:c.86-1815G=	ENSP00000509820.1:n.86-1815G=
ENST00000685857.1:n.264-283G=
ENST00000686242.1:c.86-1815G=	ENSP00000508950.1:n.86-1815G=
ENST00000686888.1:c.86-283G=	ENSP00000509619.1:n.86-283G=
ENST00000687699.1:c.210-283G=	ENSP00000508878.1:n.210-283G=
ENST00000687786.1:n.1136G=
ENST00000688588.1:c.86-283G=	ENSP00000510802.1:n.86-283G=
ENST00000688927.1:n.264-283G=
ENST00000689283.1:c.209+1739G=	ENSP00000509050.1:n.209+1739G=
ENST00000689477.1:c.86-66G=	ENSP00000508945.1:n.86-66G=
ENST00000689765.1:c.86-1815G=	ENSP00000509625.1:n.86-1815G=
ENST00000690512.1:c.86-1324G=	ENSP00000509793.1:n.86-1324G=
ENST00000692039.1:c.86-197G=	ENSP00000508821.1:n.86-197G=
ENST00000692336.1:c.86-283G=	ENSP00000508540.1:n.86-283G=
ENST00000693133.1:n.225+1739G=
ENST00000263578.10:c.86-283G= MANE Select	ENSP00000263578.5:n.86-283G=
ENST00000263578.9:c.86-283G=	ENSP00000263578.5:n.86-283G=
ENST00000524751.5:n.222+1739G=
ENST00000525083.5:n.122-1815G=
ENST00000525770.5:c.86-1815G=	ENSP00000434739.1:n.86-1815G=
ENST00000526366.5:n.101-565G=
ENST00000526525.1:n.245+1739G=
ENST00000527004.5:c.86-283G=	ENSP00000436374.1:n.86-283G=
ENST00000529802.1:n.136-283G=
ENST00000532101.5:n.92-66G=
ENST00000532125.1:c.44-283G=	ENSP00000434178.1:n.44-283G=
ENST00000533839.5:n.237+1863G=
ENST00000534011.5:n.158-1324G=
ENST00000534315.5:n.210G=
NM_017547.3:c.86-283G=	NP_060017.1:n.86-283G=
NR_037647.1:n.253-1815G=
NR_037648.1:n.272-283G=
XM_006718880.2:c.-736G=	XP_006718943.1:n.-736G=
XM_006718881.2:c.-232-1815G=	XP_006718944.1:n.-232-1815G=
XM_011542895.1:c.-642-66G=	XP_011541197.1:n.-642-66G=
XM_011542896.1:c.-445-283G=	XP_011541198.1:n.-445-283G=
XM_006718881.3:c.-232-1815G=	XP_006718944.1:n.-232-1815G=
XM_011542895.2:c.-642-66G=	XP_011541197.1:n.-642-66G=
XM_011542896.2:c.-445-283G=	XP_011541198.1:n.-445-283G=
XM_017018000.2:c.86-283G=	XP_016873489.1:n.86-283G=
XM_017018001.1:c.-445-283G=	XP_016873490.1:n.-445-283G=
XM_017018002.1:c.-224-1815G=	XP_016873491.1:n.-224-1815G=
XM_017018003.2:c.-453-283G=	XP_016873492.1:n.-453-283G=
XM_017018004.1:c.-670-66G=	XP_016873493.1:n.-670-66G=
XM_017018005.1:c.-934G=	XP_016873494.1:n.-934G=
XM_017018006.2:c.-453-283G=	XP_016873495.1:n.-453-283G=
NM_017547.4:c.86-283G= MANE Select	NP_060017.1:n.86-283G=
NR_037647.2:n.139-1815G=
NR_037648.2:n.263-283G=