Canonical Allele Identifier: CA383230201

Gene: FOXRED1

Linked Data

• gnomAD v4: 11-126275389-C-G
• MyVariant Identifiers: chr11:g.126145284C>G (hg19) ; chr11:g.126275389C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275389C>G , CM000673.2:g.126275389C>G	GRCh38
NC_000011.9:g.126145284C>G , CM000673.1:g.126145284C>G	GRCh37
NC_000011.8:g.125650494C>G	NCBI36
NG_028029.1:g.11350C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000525083.6:n.1177C>G
ENST00000532101.6:n.796C>G
ENST00000532125.2:c.691C>G	ENSP00000434178.2:p.Gln231Glu
ENST00000533839.6:c.86-405C>G	ENSP00000509952.1:n.86-405C>G
ENST00000534011.6:n.986C>G
ENST00000685484.1:c.694C>G	ENSP00000510622.1:p.Gln232Glu
ENST00000685601.1:c.694C>G	ENSP00000510603.1:p.Gln232Glu
ENST00000685765.1:c.694C>G	ENSP00000509991.1:p.Gln232Glu
ENST00000685844.1:c.*231C>G	ENSP00000509820.1:n.*231C>G
ENST00000685857.1:n.1433C>G
ENST00000686242.1:c.493C>G	ENSP00000508950.1:n.493C>G
ENST00000686888.1:c.*261C>G	ENSP00000509619.1:n.*261C>G
ENST00000687699.1:c.818C>G	ENSP00000508878.1:n.818C>G
ENST00000687786.1:n.2130C>G
ENST00000688100.1:n.1615C>G
ENST00000688588.1:c.694C>G	ENSP00000510802.1:p.Gln232Glu
ENST00000688927.1:n.2905C>G
ENST00000689283.1:c.*357C>G	ENSP00000509050.1:n.*357C>G
ENST00000689477.1:c.*587C>G	ENSP00000508945.1:n.*587C>G
ENST00000689765.1:c.*187C>G	ENSP00000509625.1:n.*187C>G
ENST00000690512.1:c.*545C>G	ENSP00000509793.1:n.*545C>G
ENST00000692039.1:c.*492C>G	ENSP00000508821.1:n.*492C>G
ENST00000692336.1:c.718C>G	ENSP00000508540.1:p.Gln240Glu
ENST00000693133.1:n.1174C>G
ENST00000263578.10:c.694C>G MANE Select	ENSP00000263578.5:p.Gln232Glu
ENST00000263578.9:c.694C>G	ENSP00000263578.5:p.Gln232Glu
ENST00000525083.5:n.414C>G
ENST00000525770.5:c.*326C>G	ENSP00000434739.1:n.*326C>G
ENST00000527004.5:c.*38C>G	ENSP00000436374.1:n.*38C>G
ENST00000530642.1:n.1476C>G
ENST00000532101.5:n.917C>G
ENST00000532125.1:c.652C>G	ENSP00000434178.1:p.Gln218Glu
ENST00000533395.5:n.427C>G
ENST00000533839.5:n.238-405C>G
ENST00000534011.5:n.746C>G
ENST00000534315.5:n.1006C>G
NM_017547.3:c.694C>G	NP_060017.1:p.Gln232Glu
NR_037647.1:n.640C>G
NR_037648.1:n.880C>G
XM_006718879.2:c.184C>G	XP_006718942.1:p.Gln62Glu
XM_006718880.2:c.61C>G	XP_006718943.1:p.Gln21Glu
XM_006718881.2:c.61C>G	XP_006718944.1:p.Gln21Glu
XM_011542895.1:c.184C>G	XP_011541197.1:p.Gln62Glu
XM_011542896.1:c.184C>G	XP_011541198.1:p.Gln62Glu
XM_006718879.3:c.184C>G	XP_006718942.1:p.Gln62Glu
XM_006718881.3:c.61C>G	XP_006718944.1:p.Gln21Glu
XM_011542895.2:c.184C>G	XP_011541197.1:p.Gln62Glu
XM_011542896.2:c.184C>G	XP_011541198.1:p.Gln62Glu
XM_017018000.2:c.694C>G	XP_016873489.1:p.Gln232Glu
XM_017018001.1:c.184C>G	XP_016873490.1:p.Gln62Glu
XM_017018002.1:c.184C>G	XP_016873491.1:p.Gln62Glu
XM_017018003.2:c.61C>G	XP_016873492.1:p.Gln21Glu
XM_017018004.1:c.61C>G	XP_016873493.1:p.Gln21Glu
XM_017018005.1:c.61C>G	XP_016873494.1:p.Gln21Glu
XM_017018006.2:c.61C>G	XP_016873495.1:p.Gln21Glu
NM_017547.4:c.694C>G MANE Select	NP_060017.1:p.Gln232Glu
NR_037647.2:n.526C>G
NR_037648.2:n.871C>G