Canonical Allele Identifier: CA477516017

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145250C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275355C>T , CM000673.2:g.126275355C>T	GRCh38
NC_000011.9:g.126145250C>T , CM000673.1:g.126145250C>T	GRCh37
NC_000011.8:g.125650460C>T	NCBI36
NG_028029.1:g.11316C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1143C>T
ENST00000532101.6:n.762C>T
ENST00000532125.2:c.657C>T	ENSP00000434178.2:p.Pro219=
ENST00000533839.6:c.86-439C>T	ENSP00000509952.1:n.86-439C>T
ENST00000534011.6:n.952C>T
ENST00000685484.1:c.660C>T	ENSP00000510622.1:p.Pro220=
ENST00000685601.1:c.660C>T	ENSP00000510603.1:p.Pro220=
ENST00000685765.1:c.660C>T	ENSP00000509991.1:p.Pro220=
ENST00000685844.1:c.*197C>T	ENSP00000509820.1:n.*197C>T
ENST00000685857.1:n.1399C>T
ENST00000686242.1:c.459C>T	ENSP00000508950.1:n.459C>T
ENST00000686888.1:c.*227C>T	ENSP00000509619.1:n.*227C>T
ENST00000687699.1:c.784C>T	ENSP00000508878.1:n.784C>T
ENST00000687786.1:n.2096C>T
ENST00000688100.1:n.1581C>T
ENST00000688588.1:c.660C>T	ENSP00000510802.1:p.Pro220=
ENST00000688927.1:n.2871C>T
ENST00000689283.1:c.*323C>T	ENSP00000509050.1:n.*323C>T
ENST00000689477.1:c.*553C>T	ENSP00000508945.1:n.*553C>T
ENST00000689765.1:c.*169-16C>T	ENSP00000509625.1:n.*169-16C>T
ENST00000690512.1:c.*511C>T	ENSP00000509793.1:n.*511C>T
ENST00000692039.1:c.*458C>T	ENSP00000508821.1:n.*458C>T
ENST00000692336.1:c.684C>T	ENSP00000508540.1:p.Pro228=
ENST00000693133.1:n.1140C>T
ENST00000263578.10:c.660C>T MANE Select	ENSP00000263578.5:p.Pro220=
ENST00000263578.9:c.660C>T	ENSP00000263578.5:p.Pro220=
ENST00000525083.5:n.380C>T
ENST00000525770.5:c.*292C>T	ENSP00000434739.1:n.*292C>T
ENST00000527004.5:c.*4C>T	ENSP00000436374.1:n.*4C>T
ENST00000530642.1:n.1442C>T
ENST00000532101.5:n.883C>T
ENST00000532125.1:c.618C>T	ENSP00000434178.1:p.Pro206=
ENST00000533395.5:n.393C>T
ENST00000533839.5:n.238-439C>T
ENST00000534011.5:n.712C>T
ENST00000534315.5:n.972C>T
NM_017547.3:c.660C>T	NP_060017.1:p.Pro220=
NR_037647.1:n.606C>T
NR_037648.1:n.846C>T
XM_006718879.2:c.150C>T	XP_006718942.1:p.Pro50=
XM_006718880.2:c.27C>T	XP_006718943.1:p.Pro9=
XM_006718881.2:c.27C>T	XP_006718944.1:p.Pro9=
XM_011542895.1:c.150C>T	XP_011541197.1:p.Pro50=
XM_011542896.1:c.150C>T	XP_011541198.1:p.Pro50=
XM_006718879.3:c.150C>T	XP_006718942.1:p.Pro50=
XM_006718881.3:c.27C>T	XP_006718944.1:p.Pro9=
XM_011542895.2:c.150C>T	XP_011541197.1:p.Pro50=
XM_011542896.2:c.150C>T	XP_011541198.1:p.Pro50=
XM_017018000.2:c.660C>T	XP_016873489.1:p.Pro220=
XM_017018001.1:c.150C>T	XP_016873490.1:p.Pro50=
XM_017018002.1:c.150C>T	XP_016873491.1:p.Pro50=
XM_017018003.2:c.27C>T	XP_016873492.1:p.Pro9=
XM_017018004.1:c.27C>T	XP_016873493.1:p.Pro9=
XM_017018005.1:c.27C>T	XP_016873494.1:p.Pro9=
XM_017018006.2:c.27C>T	XP_016873495.1:p.Pro9=
NM_017547.4:c.660C>T MANE Select	NP_060017.1:p.Pro220=
NR_037647.2:n.492C>T
NR_037648.2:n.837C>T