Canonical Allele Identifier: CA383229921

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126144854C>A (hg19) ; chr11:g.126274959C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274959C>A , CM000673.2:g.126274959C>A	GRCh38
NC_000011.9:g.126144854C>A , CM000673.1:g.126144854C>A	GRCh37
NC_000011.8:g.125650064C>A	NCBI36
NG_028029.1:g.10920C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.747C>A
ENST00000532101.6:n.734-368C>A
ENST00000532125.2:c.566C>A	ENSP00000434178.2:p.Pro189His
ENST00000533839.6:c.86-835C>A	ENSP00000509952.1:n.86-835C>A
ENST00000534011.6:n.861C>A
ENST00000685484.1:c.569C>A	ENSP00000510622.1:p.Pro190His
ENST00000685601.1:c.569C>A	ENSP00000510603.1:p.Pro190His
ENST00000685765.1:c.569C>A	ENSP00000509991.1:p.Pro190His
ENST00000685844.1:c.*169-368C>A	ENSP00000509820.1:n.*169-368C>A
ENST00000685857.1:n.1003C>A
ENST00000686242.1:c.368C>A	ENSP00000508950.1:n.368C>A
ENST00000686888.1:c.*136C>A	ENSP00000509619.1:n.*136C>A
ENST00000687699.1:c.693C>A	ENSP00000508878.1:n.693C>A
ENST00000687786.1:n.2068-368C>A
ENST00000688100.1:n.1490C>A
ENST00000688588.1:c.569C>A	ENSP00000510802.1:p.Pro190His
ENST00000688927.1:n.2475C>A
ENST00000689283.1:c.*232C>A	ENSP00000509050.1:n.*232C>A
ENST00000689477.1:c.*462C>A	ENSP00000508945.1:n.*462C>A
ENST00000689765.1:c.*169-412C>A	ENSP00000509625.1:n.*169-412C>A
ENST00000690512.1:c.*420C>A	ENSP00000509793.1:n.*420C>A
ENST00000692039.1:c.*367C>A	ENSP00000508821.1:n.*367C>A
ENST00000692336.1:c.593C>A	ENSP00000508540.1:p.Pro198His
ENST00000693133.1:n.744C>A
ENST00000263578.10:c.569C>A MANE Select	ENSP00000263578.5:p.Pro190His
ENST00000263578.9:c.569C>A	ENSP00000263578.5:p.Pro190His
ENST00000524751.5:n.505C>A
ENST00000525083.5:n.352-368C>A
ENST00000525770.5:c.*201C>A	ENSP00000434739.1:n.*201C>A
ENST00000526366.5:n.500C>A
ENST00000527004.5:c.534-368C>A	ENSP00000436374.1:n.534-368C>A
ENST00000527875.1:n.399C>A
ENST00000530642.1:n.1046C>A
ENST00000532101.5:n.792C>A
ENST00000532125.1:c.527C>A	ENSP00000434178.1:p.Pro176His
ENST00000533395.5:n.365-368C>A
ENST00000533839.5:n.238-835C>A
ENST00000534011.5:n.621C>A
ENST00000534315.5:n.944-368C>A
NM_017547.3:c.569C>A	NP_060017.1:p.Pro190His
NR_037647.1:n.515C>A
NR_037648.1:n.755C>A
XM_006718879.2:c.59C>A	XP_006718942.1:p.Pro20His
XM_006718880.2:c.-2-368C>A	XP_006718943.1:n.-2-368C>A
XM_006718881.2:c.-2-368C>A	XP_006718944.1:n.-2-368C>A
XM_011542895.1:c.59C>A	XP_011541197.1:p.Pro20His
XM_011542896.1:c.59C>A	XP_011541198.1:p.Pro20His
XM_006718879.3:c.59C>A	XP_006718942.1:p.Pro20His
XM_006718881.3:c.-2-368C>A	XP_006718944.1:n.-2-368C>A
XM_011542895.2:c.59C>A	XP_011541197.1:p.Pro20His
XM_011542896.2:c.59C>A	XP_011541198.1:p.Pro20His
XM_017018000.2:c.569C>A	XP_016873489.1:p.Pro190His
XM_017018001.1:c.59C>A	XP_016873490.1:p.Pro20His
XM_017018002.1:c.59C>A	XP_016873491.1:p.Pro20His
XM_017018003.2:c.-2-368C>A	XP_016873492.1:n.-2-368C>A
XM_017018004.1:c.-2-368C>A	XP_016873493.1:n.-2-368C>A
XM_017018005.1:c.-2-368C>A	XP_016873494.1:n.-2-368C>A
XM_017018006.2:c.-2-368C>A	XP_016873495.1:n.-2-368C>A
NM_017547.4:c.569C>A MANE Select	NP_060017.1:p.Pro190His
NR_037647.2:n.401C>A
NR_037648.2:n.746C>A