Canonical Allele Identifier: CA477515341

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126144897A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275002A>T , CM000673.2:g.126275002A>T	GRCh38
NC_000011.9:g.126144897A>T , CM000673.1:g.126144897A>T	GRCh37
NC_000011.8:g.125650107A>T	NCBI36
NG_028029.1:g.10963A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.790A>T
ENST00000532101.6:n.734-325A>T
ENST00000532125.2:c.609A>T	ENSP00000434178.2:p.Gly203=
ENST00000533839.6:c.86-792A>T	ENSP00000509952.1:n.86-792A>T
ENST00000534011.6:n.904A>T
ENST00000685484.1:c.612A>T	ENSP00000510622.1:p.Gly204=
ENST00000685601.1:c.612A>T	ENSP00000510603.1:p.Gly204=
ENST00000685765.1:c.612A>T	ENSP00000509991.1:p.Gly204=
ENST00000685844.1:c.*169-325A>T	ENSP00000509820.1:n.*169-325A>T
ENST00000685857.1:n.1046A>T
ENST00000686242.1:c.411A>T	ENSP00000508950.1:n.411A>T
ENST00000686888.1:c.*179A>T	ENSP00000509619.1:n.*179A>T
ENST00000687699.1:c.736A>T	ENSP00000508878.1:n.736A>T
ENST00000687786.1:n.2068-325A>T
ENST00000688100.1:n.1533A>T
ENST00000688588.1:c.612A>T	ENSP00000510802.1:p.Gly204=
ENST00000688927.1:n.2518A>T
ENST00000689283.1:c.*275A>T	ENSP00000509050.1:n.*275A>T
ENST00000689477.1:c.*505A>T	ENSP00000508945.1:n.*505A>T
ENST00000689765.1:c.*169-369A>T	ENSP00000509625.1:n.*169-369A>T
ENST00000690512.1:c.*463A>T	ENSP00000509793.1:n.*463A>T
ENST00000692039.1:c.*410A>T	ENSP00000508821.1:n.*410A>T
ENST00000692336.1:c.636A>T	ENSP00000508540.1:p.Gly212=
ENST00000693133.1:n.787A>T
ENST00000263578.10:c.612A>T MANE Select	ENSP00000263578.5:p.Gly204=
ENST00000263578.9:c.612A>T	ENSP00000263578.5:p.Gly204=
ENST00000524751.5:n.548A>T
ENST00000525083.5:n.352-325A>T
ENST00000525770.5:c.*244A>T	ENSP00000434739.1:n.*244A>T
ENST00000526366.5:n.543A>T
ENST00000527004.5:c.534-325A>T	ENSP00000436374.1:n.534-325A>T
ENST00000527875.1:n.442A>T
ENST00000530642.1:n.1089A>T
ENST00000532101.5:n.835A>T
ENST00000532125.1:c.570A>T	ENSP00000434178.1:p.Gly190=
ENST00000533395.5:n.365-325A>T
ENST00000533839.5:n.238-792A>T
ENST00000534011.5:n.664A>T
ENST00000534315.5:n.944-325A>T
NM_017547.3:c.612A>T	NP_060017.1:p.Gly204=
NR_037647.1:n.558A>T
NR_037648.1:n.798A>T
XM_006718879.2:c.102A>T	XP_006718942.1:p.Gly34=
XM_006718880.2:c.-2-325A>T	XP_006718943.1:n.-2-325A>T
XM_006718881.2:c.-2-325A>T	XP_006718944.1:n.-2-325A>T
XM_011542895.1:c.102A>T	XP_011541197.1:p.Gly34=
XM_011542896.1:c.102A>T	XP_011541198.1:p.Gly34=
XM_006718879.3:c.102A>T	XP_006718942.1:p.Gly34=
XM_006718881.3:c.-2-325A>T	XP_006718944.1:n.-2-325A>T
XM_011542895.2:c.102A>T	XP_011541197.1:p.Gly34=
XM_011542896.2:c.102A>T	XP_011541198.1:p.Gly34=
XM_017018000.2:c.612A>T	XP_016873489.1:p.Gly204=
XM_017018001.1:c.102A>T	XP_016873490.1:p.Gly34=
XM_017018002.1:c.102A>T	XP_016873491.1:p.Gly34=
XM_017018003.2:c.-2-325A>T	XP_016873492.1:n.-2-325A>T
XM_017018004.1:c.-2-325A>T	XP_016873493.1:n.-2-325A>T
XM_017018005.1:c.-2-325A>T	XP_016873494.1:n.-2-325A>T
XM_017018006.2:c.-2-325A>T	XP_016873495.1:n.-2-325A>T
NM_017547.4:c.612A>T MANE Select	NP_060017.1:p.Gly204=
NR_037647.2:n.444A>T
NR_037648.2:n.789A>T