Canonical Allele Identifier: CA477516106

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145304C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275409C>T , CM000673.2:g.126275409C>T	GRCh38
NC_000011.9:g.126145304C>T , CM000673.1:g.126145304C>T	GRCh37
NC_000011.8:g.125650514C>T	NCBI36
NG_028029.1:g.11370C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1197C>T
ENST00000532101.6:n.816C>T
ENST00000532125.2:c.711C>T	ENSP00000434178.2:p.Phe237=
ENST00000533839.6:c.86-385C>T	ENSP00000509952.1:n.86-385C>T
ENST00000534011.6:n.1006C>T
ENST00000685484.1:c.714C>T	ENSP00000510622.1:p.Phe238=
ENST00000685601.1:c.714C>T	ENSP00000510603.1:p.Phe238=
ENST00000685765.1:c.714C>T	ENSP00000509991.1:p.Phe238=
ENST00000685844.1:c.*251C>T	ENSP00000509820.1:n.*251C>T
ENST00000685857.1:n.1453C>T
ENST00000686242.1:c.513C>T	ENSP00000508950.1:n.513C>T
ENST00000686888.1:c.*281C>T	ENSP00000509619.1:n.*281C>T
ENST00000687699.1:c.838C>T	ENSP00000508878.1:n.838C>T
ENST00000687786.1:n.2150C>T
ENST00000688100.1:n.1635C>T
ENST00000688588.1:c.714C>T	ENSP00000510802.1:p.Phe238=
ENST00000688927.1:n.2925C>T
ENST00000689283.1:c.*377C>T	ENSP00000509050.1:n.*377C>T
ENST00000689477.1:c.*607C>T	ENSP00000508945.1:n.*607C>T
ENST00000689765.1:c.*207C>T	ENSP00000509625.1:n.*207C>T
ENST00000690512.1:c.*565C>T	ENSP00000509793.1:n.*565C>T
ENST00000692039.1:c.*512C>T	ENSP00000508821.1:n.*512C>T
ENST00000692336.1:c.738C>T	ENSP00000508540.1:p.Phe246=
ENST00000693133.1:n.1194C>T
ENST00000263578.10:c.714C>T MANE Select	ENSP00000263578.5:p.Phe238=
ENST00000263578.9:c.714C>T	ENSP00000263578.5:p.Phe238=
ENST00000525083.5:n.434C>T
ENST00000525770.5:c.*346C>T	ENSP00000434739.1:n.*346C>T
ENST00000527004.5:c.*58C>T	ENSP00000436374.1:n.*58C>T
ENST00000530642.1:n.1496C>T
ENST00000532101.5:n.937C>T
ENST00000532125.1:c.672C>T	ENSP00000434178.1:p.Phe224=
ENST00000533395.5:n.447C>T
ENST00000533839.5:n.238-385C>T
ENST00000534011.5:n.766C>T
ENST00000534315.5:n.1026C>T
NM_017547.3:c.714C>T	NP_060017.1:p.Phe238=
NR_037647.1:n.660C>T
NR_037648.1:n.900C>T
XM_006718879.2:c.204C>T	XP_006718942.1:p.Phe68=
XM_006718880.2:c.81C>T	XP_006718943.1:p.Phe27=
XM_006718881.2:c.81C>T	XP_006718944.1:p.Phe27=
XM_011542895.1:c.204C>T	XP_011541197.1:p.Phe68=
XM_011542896.1:c.204C>T	XP_011541198.1:p.Phe68=
XM_006718879.3:c.204C>T	XP_006718942.1:p.Phe68=
XM_006718881.3:c.81C>T	XP_006718944.1:p.Phe27=
XM_011542895.2:c.204C>T	XP_011541197.1:p.Phe68=
XM_011542896.2:c.204C>T	XP_011541198.1:p.Phe68=
XM_017018000.2:c.714C>T	XP_016873489.1:p.Phe238=
XM_017018001.1:c.204C>T	XP_016873490.1:p.Phe68=
XM_017018002.1:c.204C>T	XP_016873491.1:p.Phe68=
XM_017018003.2:c.81C>T	XP_016873492.1:p.Phe27=
XM_017018004.1:c.81C>T	XP_016873493.1:p.Phe27=
XM_017018005.1:c.81C>T	XP_016873494.1:p.Phe27=
XM_017018006.2:c.81C>T	XP_016873495.1:p.Phe27=
NM_017547.4:c.714C>T MANE Select	NP_060017.1:p.Phe238=
NR_037647.2:n.546C>T
NR_037648.2:n.891C>T