Canonical Allele Identifier: CA383230046

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126144911C>T (hg19) ; chr11:g.126275016C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275016C>T , CM000673.2:g.126275016C>T	GRCh38
NC_000011.9:g.126144911C>T , CM000673.1:g.126144911C>T	GRCh37
NC_000011.8:g.125650121C>T	NCBI36
NG_028029.1:g.10977C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.804C>T
ENST00000532101.6:n.734-311C>T
ENST00000532125.2:c.623C>T	ENSP00000434178.2:p.Ser208Phe
ENST00000533839.6:c.86-778C>T	ENSP00000509952.1:n.86-778C>T
ENST00000534011.6:n.918C>T
ENST00000685484.1:c.626C>T	ENSP00000510622.1:p.Ser209Phe
ENST00000685601.1:c.626C>T	ENSP00000510603.1:p.Ser209Phe
ENST00000685765.1:c.626C>T	ENSP00000509991.1:p.Ser209Phe
ENST00000685844.1:c.*169-311C>T	ENSP00000509820.1:n.*169-311C>T
ENST00000685857.1:n.1060C>T
ENST00000686242.1:c.425C>T	ENSP00000508950.1:n.425C>T
ENST00000686888.1:c.*193C>T	ENSP00000509619.1:n.*193C>T
ENST00000687699.1:c.750C>T	ENSP00000508878.1:n.750C>T
ENST00000687786.1:n.2068-311C>T
ENST00000688100.1:n.1547C>T
ENST00000688588.1:c.626C>T	ENSP00000510802.1:p.Ser209Phe
ENST00000688927.1:n.2532C>T
ENST00000689283.1:c.*289C>T	ENSP00000509050.1:n.*289C>T
ENST00000689477.1:c.*519C>T	ENSP00000508945.1:n.*519C>T
ENST00000689765.1:c.*169-355C>T	ENSP00000509625.1:n.*169-355C>T
ENST00000690512.1:c.*477C>T	ENSP00000509793.1:n.*477C>T
ENST00000692039.1:c.*424C>T	ENSP00000508821.1:n.*424C>T
ENST00000692336.1:c.650C>T	ENSP00000508540.1:p.Ser217Phe
ENST00000693133.1:n.801C>T
ENST00000263578.10:c.626C>T MANE Select	ENSP00000263578.5:p.Ser209Phe
ENST00000263578.9:c.626C>T	ENSP00000263578.5:p.Ser209Phe
ENST00000524751.5:n.562C>T
ENST00000525083.5:n.352-311C>T
ENST00000525770.5:c.*258C>T	ENSP00000434739.1:n.*258C>T
ENST00000527004.5:c.534-311C>T	ENSP00000436374.1:n.534-311C>T
ENST00000527875.1:n.456C>T
ENST00000530642.1:n.1103C>T
ENST00000532101.5:n.849C>T
ENST00000532125.1:c.584C>T	ENSP00000434178.1:p.Ser195Phe
ENST00000533395.5:n.365-311C>T
ENST00000533839.5:n.238-778C>T
ENST00000534011.5:n.678C>T
ENST00000534315.5:n.944-311C>T
NM_017547.3:c.626C>T	NP_060017.1:p.Ser209Phe
NR_037647.1:n.572C>T
NR_037648.1:n.812C>T
XM_006718879.2:c.116C>T	XP_006718942.1:p.Ser39Phe
XM_006718880.2:c.-2-311C>T	XP_006718943.1:n.-2-311C>T
XM_006718881.2:c.-2-311C>T	XP_006718944.1:n.-2-311C>T
XM_011542895.1:c.116C>T	XP_011541197.1:p.Ser39Phe
XM_011542896.1:c.116C>T	XP_011541198.1:p.Ser39Phe
XM_006718879.3:c.116C>T	XP_006718942.1:p.Ser39Phe
XM_006718881.3:c.-2-311C>T	XP_006718944.1:n.-2-311C>T
XM_011542895.2:c.116C>T	XP_011541197.1:p.Ser39Phe
XM_011542896.2:c.116C>T	XP_011541198.1:p.Ser39Phe
XM_017018000.2:c.626C>T	XP_016873489.1:p.Ser209Phe
XM_017018001.1:c.116C>T	XP_016873490.1:p.Ser39Phe
XM_017018002.1:c.116C>T	XP_016873491.1:p.Ser39Phe
XM_017018003.2:c.-2-311C>T	XP_016873492.1:n.-2-311C>T
XM_017018004.1:c.-2-311C>T	XP_016873493.1:n.-2-311C>T
XM_017018005.1:c.-2-311C>T	XP_016873494.1:n.-2-311C>T
XM_017018006.2:c.-2-311C>T	XP_016873495.1:n.-2-311C>T
NM_017547.4:c.626C>T MANE Select	NP_060017.1:p.Ser209Phe
NR_037647.2:n.458C>T
NR_037648.2:n.803C>T