Canonical Allele Identifier: CA113792
Gene: FOXRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 5
dbSNP Id: rs267606829

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000525083.6:n.1177C>T
ENST00000532101.6:n.796C>T
ENST00000532125.2:c.691C>T ENSP00000434178.2:p.Gln231Ter
ENST00000533839.6:c.86-405C>T ENSP00000509952.1:n.86-405C>T
ENST00000534011.6:n.986C>T
ENST00000685484.1:c.694C>T ENSP00000510622.1:p.Gln232Ter
ENST00000685601.1:c.694C>T ENSP00000510603.1:p.Gln232Ter
ENST00000685765.1:c.694C>T ENSP00000509991.1:p.Gln232Ter
ENST00000685844.1:c.*231C>T ENSP00000509820.1:n.*231C>T
ENST00000685857.1:n.1433C>T
ENST00000686242.1:c.493C>T ENSP00000508950.1:n.493C>T
ENST00000686888.1:c.*261C>T ENSP00000509619.1:n.*261C>T
ENST00000687699.1:c.818C>T ENSP00000508878.1:n.818C>T
ENST00000687786.1:n.2130C>T
ENST00000688100.1:n.1615C>T
ENST00000688588.1:c.694C>T ENSP00000510802.1:p.Gln232Ter
ENST00000688927.1:n.2905C>T
ENST00000689283.1:c.*357C>T ENSP00000509050.1:n.*357C>T
ENST00000689477.1:c.*587C>T ENSP00000508945.1:n.*587C>T
ENST00000689765.1:c.*187C>T ENSP00000509625.1:n.*187C>T
ENST00000690512.1:c.*545C>T ENSP00000509793.1:n.*545C>T
ENST00000692039.1:c.*492C>T ENSP00000508821.1:n.*492C>T
ENST00000692336.1:c.718C>T ENSP00000508540.1:p.Gln240Ter
ENST00000693133.1:n.1174C>T
ENST00000263578.10:c.694C>T MANE Select ENSP00000263578.5:p.Gln232Ter
ENST00000263578.9:c.694C>T ENSP00000263578.5:p.Gln232Ter
ENST00000525083.5:n.414C>T
ENST00000525770.5:c.*326C>T ENSP00000434739.1:n.*326C>T
ENST00000527004.5:c.*38C>T ENSP00000436374.1:n.*38C>T
ENST00000530642.1:n.1476C>T
ENST00000532101.5:n.917C>T
ENST00000532125.1:c.652C>T ENSP00000434178.1:p.Gln218Ter
ENST00000533395.5:n.427C>T
ENST00000533839.5:n.238-405C>T
ENST00000534011.5:n.746C>T
ENST00000534315.5:n.1006C>T
NM_017547.3:c.694C>T NP_060017.1:p.Gln232Ter
NR_037647.1:n.640C>T
NR_037648.1:n.880C>T
XM_006718879.2:c.184C>T XP_006718942.1:p.Gln62Ter
XM_006718880.2:c.61C>T XP_006718943.1:p.Gln21Ter
XM_006718881.2:c.61C>T XP_006718944.1:p.Gln21Ter
XM_011542895.1:c.184C>T XP_011541197.1:p.Gln62Ter
XM_011542896.1:c.184C>T XP_011541198.1:p.Gln62Ter
XM_006718879.3:c.184C>T XP_006718942.1:p.Gln62Ter
XM_006718881.3:c.61C>T XP_006718944.1:p.Gln21Ter
XM_011542895.2:c.184C>T XP_011541197.1:p.Gln62Ter
XM_011542896.2:c.184C>T XP_011541198.1:p.Gln62Ter
XM_017018000.2:c.694C>T XP_016873489.1:p.Gln232Ter
XM_017018001.1:c.184C>T XP_016873490.1:p.Gln62Ter
XM_017018002.1:c.184C>T XP_016873491.1:p.Gln62Ter
XM_017018003.2:c.61C>T XP_016873492.1:p.Gln21Ter
XM_017018004.1:c.61C>T XP_016873493.1:p.Gln21Ter
XM_017018005.1:c.61C>T XP_016873494.1:p.Gln21Ter
XM_017018006.2:c.61C>T XP_016873495.1:p.Gln21Ter
NM_017547.4:c.694C>T MANE Select NP_060017.1:p.Gln232Ter
NR_037647.2:n.526C>T
NR_037648.2:n.871C>T