Canonical Allele Identifier: CA477516109

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145313A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275418A>C , CM000673.2:g.126275418A>C	GRCh38
NC_000011.9:g.126145313A>C , CM000673.1:g.126145313A>C	GRCh37
NC_000011.8:g.125650523A>C	NCBI36
NG_028029.1:g.11379A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1206A>C
ENST00000532101.6:n.825A>C
ENST00000532125.2:c.720A>C	ENSP00000434178.2:p.Gly240=
ENST00000533839.6:c.86-376A>C	ENSP00000509952.1:n.86-376A>C
ENST00000534011.6:n.1015A>C
ENST00000685484.1:c.723A>C	ENSP00000510622.1:p.Gly241=
ENST00000685601.1:c.723A>C	ENSP00000510603.1:p.Gly241=
ENST00000685765.1:c.723A>C	ENSP00000509991.1:p.Gly241=
ENST00000685844.1:c.*260A>C	ENSP00000509820.1:n.*260A>C
ENST00000685857.1:n.1462A>C
ENST00000686242.1:c.522A>C	ENSP00000508950.1:n.522A>C
ENST00000686888.1:c.*290A>C	ENSP00000509619.1:n.*290A>C
ENST00000687699.1:c.847A>C	ENSP00000508878.1:n.847A>C
ENST00000687786.1:n.2159A>C
ENST00000688100.1:n.1644A>C
ENST00000688588.1:c.723A>C	ENSP00000510802.1:p.Gly241=
ENST00000688927.1:n.2934A>C
ENST00000689283.1:c.*386A>C	ENSP00000509050.1:n.*386A>C
ENST00000689477.1:c.*616A>C	ENSP00000508945.1:n.*616A>C
ENST00000689765.1:c.*216A>C	ENSP00000509625.1:n.*216A>C
ENST00000690512.1:c.*574A>C	ENSP00000509793.1:n.*574A>C
ENST00000692039.1:c.*521A>C	ENSP00000508821.1:n.*521A>C
ENST00000692336.1:c.747A>C	ENSP00000508540.1:p.Gly249=
ENST00000693133.1:n.1203A>C
ENST00000263578.10:c.723A>C MANE Select	ENSP00000263578.5:p.Gly241=
ENST00000263578.9:c.723A>C	ENSP00000263578.5:p.Gly241=
ENST00000525083.5:n.443A>C
ENST00000525770.5:c.*355A>C	ENSP00000434739.1:n.*355A>C
ENST00000527004.5:c.*67A>C	ENSP00000436374.1:n.*67A>C
ENST00000530642.1:n.1505A>C
ENST00000532101.5:n.946A>C
ENST00000532125.1:c.681A>C	ENSP00000434178.1:p.Gly227=
ENST00000533395.5:n.456A>C
ENST00000533839.5:n.238-376A>C
ENST00000534011.5:n.775A>C
ENST00000534315.5:n.1035A>C
NM_017547.3:c.723A>C	NP_060017.1:p.Gly241=
NR_037647.1:n.669A>C
NR_037648.1:n.909A>C
XM_006718879.2:c.213A>C	XP_006718942.1:p.Gly71=
XM_006718880.2:c.90A>C	XP_006718943.1:p.Gly30=
XM_006718881.2:c.90A>C	XP_006718944.1:p.Gly30=
XM_011542895.1:c.213A>C	XP_011541197.1:p.Gly71=
XM_011542896.1:c.213A>C	XP_011541198.1:p.Gly71=
XM_006718879.3:c.213A>C	XP_006718942.1:p.Gly71=
XM_006718881.3:c.90A>C	XP_006718944.1:p.Gly30=
XM_011542895.2:c.213A>C	XP_011541197.1:p.Gly71=
XM_011542896.2:c.213A>C	XP_011541198.1:p.Gly71=
XM_017018000.2:c.723A>C	XP_016873489.1:p.Gly241=
XM_017018001.1:c.213A>C	XP_016873490.1:p.Gly71=
XM_017018002.1:c.213A>C	XP_016873491.1:p.Gly71=
XM_017018003.2:c.90A>C	XP_016873492.1:p.Gly30=
XM_017018004.1:c.90A>C	XP_016873493.1:p.Gly30=
XM_017018005.1:c.90A>C	XP_016873494.1:p.Gly30=
XM_017018006.2:c.90A>C	XP_016873495.1:p.Gly30=
NM_017547.4:c.723A>C MANE Select	NP_060017.1:p.Gly241=
NR_037647.2:n.555A>C
NR_037648.2:n.900A>C