Canonical Allele Identifier: CA383229948

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126144868A>G (hg19) ; chr11:g.126274973A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274973A>G , CM000673.2:g.126274973A>G	GRCh38
NC_000011.9:g.126144868A>G , CM000673.1:g.126144868A>G	GRCh37
NC_000011.8:g.125650078A>G	NCBI36
NG_028029.1:g.10934A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.761A>G
ENST00000532101.6:n.734-354A>G
ENST00000532125.2:c.580A>G	ENSP00000434178.2:p.Asn194Asp
ENST00000533839.6:c.86-821A>G	ENSP00000509952.1:n.86-821A>G
ENST00000534011.6:n.875A>G
ENST00000685484.1:c.583A>G	ENSP00000510622.1:p.Asn195Asp
ENST00000685601.1:c.583A>G	ENSP00000510603.1:p.Asn195Asp
ENST00000685765.1:c.583A>G	ENSP00000509991.1:p.Asn195Asp
ENST00000685844.1:c.*169-354A>G	ENSP00000509820.1:n.*169-354A>G
ENST00000685857.1:n.1017A>G
ENST00000686242.1:c.382A>G	ENSP00000508950.1:n.382A>G
ENST00000686888.1:c.*150A>G	ENSP00000509619.1:n.*150A>G
ENST00000687699.1:c.707A>G	ENSP00000508878.1:n.707A>G
ENST00000687786.1:n.2068-354A>G
ENST00000688100.1:n.1504A>G
ENST00000688588.1:c.583A>G	ENSP00000510802.1:p.Asn195Asp
ENST00000688927.1:n.2489A>G
ENST00000689283.1:c.*246A>G	ENSP00000509050.1:n.*246A>G
ENST00000689477.1:c.*476A>G	ENSP00000508945.1:n.*476A>G
ENST00000689765.1:c.*169-398A>G	ENSP00000509625.1:n.*169-398A>G
ENST00000690512.1:c.*434A>G	ENSP00000509793.1:n.*434A>G
ENST00000692039.1:c.*381A>G	ENSP00000508821.1:n.*381A>G
ENST00000692336.1:c.607A>G	ENSP00000508540.1:p.Asn203Asp
ENST00000693133.1:n.758A>G
ENST00000263578.10:c.583A>G MANE Select	ENSP00000263578.5:p.Asn195Asp
ENST00000263578.9:c.583A>G	ENSP00000263578.5:p.Asn195Asp
ENST00000524751.5:n.519A>G
ENST00000525083.5:n.352-354A>G
ENST00000525770.5:c.*215A>G	ENSP00000434739.1:n.*215A>G
ENST00000526366.5:n.514A>G
ENST00000527004.5:c.534-354A>G	ENSP00000436374.1:n.534-354A>G
ENST00000527875.1:n.413A>G
ENST00000530642.1:n.1060A>G
ENST00000532101.5:n.806A>G
ENST00000532125.1:c.541A>G	ENSP00000434178.1:p.Asn181Asp
ENST00000533395.5:n.365-354A>G
ENST00000533839.5:n.238-821A>G
ENST00000534011.5:n.635A>G
ENST00000534315.5:n.944-354A>G
NM_017547.3:c.583A>G	NP_060017.1:p.Asn195Asp
NR_037647.1:n.529A>G
NR_037648.1:n.769A>G
XM_006718879.2:c.73A>G	XP_006718942.1:p.Asn25Asp
XM_006718880.2:c.-2-354A>G	XP_006718943.1:n.-2-354A>G
XM_006718881.2:c.-2-354A>G	XP_006718944.1:n.-2-354A>G
XM_011542895.1:c.73A>G	XP_011541197.1:p.Asn25Asp
XM_011542896.1:c.73A>G	XP_011541198.1:p.Asn25Asp
XM_006718879.3:c.73A>G	XP_006718942.1:p.Asn25Asp
XM_006718881.3:c.-2-354A>G	XP_006718944.1:n.-2-354A>G
XM_011542895.2:c.73A>G	XP_011541197.1:p.Asn25Asp
XM_011542896.2:c.73A>G	XP_011541198.1:p.Asn25Asp
XM_017018000.2:c.583A>G	XP_016873489.1:p.Asn195Asp
XM_017018001.1:c.73A>G	XP_016873490.1:p.Asn25Asp
XM_017018002.1:c.73A>G	XP_016873491.1:p.Asn25Asp
XM_017018003.2:c.-2-354A>G	XP_016873492.1:n.-2-354A>G
XM_017018004.1:c.-2-354A>G	XP_016873493.1:n.-2-354A>G
XM_017018005.1:c.-2-354A>G	XP_016873494.1:n.-2-354A>G
XM_017018006.2:c.-2-354A>G	XP_016873495.1:n.-2-354A>G
NM_017547.4:c.583A>G MANE Select	NP_060017.1:p.Asn195Asp
NR_037647.2:n.415A>G
NR_037648.2:n.760A>G