Canonical Allele Identifier: CA2007079707
Gene: FOXRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126275369A= , CM000673.2:g.126275369A= GRCh38
NC_000011.9:g.126145264A= , CM000673.1:g.126145264A= GRCh37
NC_000011.8:g.125650474A= NCBI36
NG_028029.1:g.11330A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.1157A=
ENST00000532101.6:n.776A=
ENST00000532125.2:c.671A= ENSP00000434178.2:p.Gln224=
ENST00000533839.6:c.86-425A= ENSP00000509952.1:n.86-425A=
ENST00000534011.6:n.966A=
ENST00000685484.1:c.674A= ENSP00000510622.1:p.Gln225=
ENST00000685601.1:c.674A= ENSP00000510603.1:p.Gln225=
ENST00000685765.1:c.674A= ENSP00000509991.1:p.Gln225=
ENST00000685844.1:c.*211A= ENSP00000509820.1:n.*211A=
ENST00000685857.1:n.1413A=
ENST00000686242.1:c.473A= ENSP00000508950.1:n.473A=
ENST00000686888.1:c.*241A= ENSP00000509619.1:n.*241A=
ENST00000687699.1:c.798A= ENSP00000508878.1:n.798A=
ENST00000687786.1:n.2110A=
ENST00000688100.1:n.1595A=
ENST00000688588.1:c.674A= ENSP00000510802.1:p.Gln225=
ENST00000688927.1:n.2885A=
ENST00000689283.1:c.*337A= ENSP00000509050.1:n.*337A=
ENST00000689477.1:c.*567A= ENSP00000508945.1:n.*567A=
ENST00000689765.1:c.*169-2A= ENSP00000509625.1:n.*169-2A=
ENST00000690512.1:c.*525A= ENSP00000509793.1:n.*525A=
ENST00000692039.1:c.*472A= ENSP00000508821.1:n.*472A=
ENST00000692336.1:c.698A= ENSP00000508540.1:p.Gln233=
ENST00000693133.1:n.1154A=
ENST00000263578.10:c.674A= MANE Select ENSP00000263578.5:p.Gln225=
ENST00000263578.9:c.674A= ENSP00000263578.5:p.Gln225=
ENST00000525083.5:n.394A=
ENST00000525770.5:c.*306A= ENSP00000434739.1:n.*306A=
ENST00000527004.5:c.*18A= ENSP00000436374.1:n.*18A=
ENST00000530642.1:n.1456A=
ENST00000532101.5:n.897A=
ENST00000532125.1:c.632A= ENSP00000434178.1:p.Gln211=
ENST00000533395.5:n.407A=
ENST00000533839.5:n.238-425A=
ENST00000534011.5:n.726A=
ENST00000534315.5:n.986A=
NM_017547.3:c.674A= NP_060017.1:p.Gln225=
NR_037647.1:n.620A=
NR_037648.1:n.860A=
XM_006718879.2:c.164A= XP_006718942.1:p.Gln55=
XM_006718880.2:c.41A= XP_006718943.1:p.Gln14=
XM_006718881.2:c.41A= XP_006718944.1:p.Gln14=
XM_011542895.1:c.164A= XP_011541197.1:p.Gln55=
XM_011542896.1:c.164A= XP_011541198.1:p.Gln55=
XM_006718879.3:c.164A= XP_006718942.1:p.Gln55=
XM_006718881.3:c.41A= XP_006718944.1:p.Gln14=
XM_011542895.2:c.164A= XP_011541197.1:p.Gln55=
XM_011542896.2:c.164A= XP_011541198.1:p.Gln55=
XM_017018000.2:c.674A= XP_016873489.1:p.Gln225=
XM_017018001.1:c.164A= XP_016873490.1:p.Gln55=
XM_017018002.1:c.164A= XP_016873491.1:p.Gln55=
XM_017018003.2:c.41A= XP_016873492.1:p.Gln14=
XM_017018004.1:c.41A= XP_016873493.1:p.Gln14=
XM_017018005.1:c.41A= XP_016873494.1:p.Gln14=
XM_017018006.2:c.41A= XP_016873495.1:p.Gln14=
NM_017547.4:c.674A= MANE Select NP_060017.1:p.Gln225=
NR_037647.2:n.506A=
NR_037648.2:n.851A=