Canonical Allele Identifier: CA477516089

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145283C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275388C>A , CM000673.2:g.126275388C>A	GRCh38
NC_000011.9:g.126145283C>A , CM000673.1:g.126145283C>A	GRCh37
NC_000011.8:g.125650493C>A	NCBI36
NG_028029.1:g.11349C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1176C>A
ENST00000532101.6:n.795C>A
ENST00000532125.2:c.690C>A	ENSP00000434178.2:p.Val230=
ENST00000533839.6:c.86-406C>A	ENSP00000509952.1:n.86-406C>A
ENST00000534011.6:n.985C>A
ENST00000685484.1:c.693C>A	ENSP00000510622.1:p.Val231=
ENST00000685601.1:c.693C>A	ENSP00000510603.1:p.Val231=
ENST00000685765.1:c.693C>A	ENSP00000509991.1:p.Val231=
ENST00000685844.1:c.*230C>A	ENSP00000509820.1:n.*230C>A
ENST00000685857.1:n.1432C>A
ENST00000686242.1:c.492C>A	ENSP00000508950.1:n.492C>A
ENST00000686888.1:c.*260C>A	ENSP00000509619.1:n.*260C>A
ENST00000687699.1:c.817C>A	ENSP00000508878.1:n.817C>A
ENST00000687786.1:n.2129C>A
ENST00000688100.1:n.1614C>A
ENST00000688588.1:c.693C>A	ENSP00000510802.1:p.Val231=
ENST00000688927.1:n.2904C>A
ENST00000689283.1:c.*356C>A	ENSP00000509050.1:n.*356C>A
ENST00000689477.1:c.*586C>A	ENSP00000508945.1:n.*586C>A
ENST00000689765.1:c.*186C>A	ENSP00000509625.1:n.*186C>A
ENST00000690512.1:c.*544C>A	ENSP00000509793.1:n.*544C>A
ENST00000692039.1:c.*491C>A	ENSP00000508821.1:n.*491C>A
ENST00000692336.1:c.717C>A	ENSP00000508540.1:p.Val239=
ENST00000693133.1:n.1173C>A
ENST00000263578.10:c.693C>A MANE Select	ENSP00000263578.5:p.Val231=
ENST00000263578.9:c.693C>A	ENSP00000263578.5:p.Val231=
ENST00000525083.5:n.413C>A
ENST00000525770.5:c.*325C>A	ENSP00000434739.1:n.*325C>A
ENST00000527004.5:c.*37C>A	ENSP00000436374.1:n.*37C>A
ENST00000530642.1:n.1475C>A
ENST00000532101.5:n.916C>A
ENST00000532125.1:c.651C>A	ENSP00000434178.1:p.Val217=
ENST00000533395.5:n.426C>A
ENST00000533839.5:n.238-406C>A
ENST00000534011.5:n.745C>A
ENST00000534315.5:n.1005C>A
NM_017547.3:c.693C>A	NP_060017.1:p.Val231=
NR_037647.1:n.639C>A
NR_037648.1:n.879C>A
XM_006718879.2:c.183C>A	XP_006718942.1:p.Val61=
XM_006718880.2:c.60C>A	XP_006718943.1:p.Val20=
XM_006718881.2:c.60C>A	XP_006718944.1:p.Val20=
XM_011542895.1:c.183C>A	XP_011541197.1:p.Val61=
XM_011542896.1:c.183C>A	XP_011541198.1:p.Val61=
XM_006718879.3:c.183C>A	XP_006718942.1:p.Val61=
XM_006718881.3:c.60C>A	XP_006718944.1:p.Val20=
XM_011542895.2:c.183C>A	XP_011541197.1:p.Val61=
XM_011542896.2:c.183C>A	XP_011541198.1:p.Val61=
XM_017018000.2:c.693C>A	XP_016873489.1:p.Val231=
XM_017018001.1:c.183C>A	XP_016873490.1:p.Val61=
XM_017018002.1:c.183C>A	XP_016873491.1:p.Val61=
XM_017018003.2:c.60C>A	XP_016873492.1:p.Val20=
XM_017018004.1:c.60C>A	XP_016873493.1:p.Val20=
XM_017018005.1:c.60C>A	XP_016873494.1:p.Val20=
XM_017018006.2:c.60C>A	XP_016873495.1:p.Val20=
NM_017547.4:c.693C>A MANE Select	NP_060017.1:p.Val231=
NR_037647.2:n.525C>A
NR_037648.2:n.870C>A