Canonical Allele Identifier: CA383230264

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145312G>C (hg19) ; chr11:g.126275417G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275417G>C , CM000673.2:g.126275417G>C	GRCh38
NC_000011.9:g.126145312G>C , CM000673.1:g.126145312G>C	GRCh37
NC_000011.8:g.125650522G>C	NCBI36
NG_028029.1:g.11378G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1205G>C
ENST00000532101.6:n.824G>C
ENST00000532125.2:c.719G>C	ENSP00000434178.2:p.Gly240Ala
ENST00000533839.6:c.86-377G>C	ENSP00000509952.1:n.86-377G>C
ENST00000534011.6:n.1014G>C
ENST00000685484.1:c.722G>C	ENSP00000510622.1:p.Gly241Ala
ENST00000685601.1:c.722G>C	ENSP00000510603.1:p.Gly241Ala
ENST00000685765.1:c.722G>C	ENSP00000509991.1:p.Gly241Ala
ENST00000685844.1:c.*259G>C	ENSP00000509820.1:n.*259G>C
ENST00000685857.1:n.1461G>C
ENST00000686242.1:c.521G>C	ENSP00000508950.1:n.521G>C
ENST00000686888.1:c.*289G>C	ENSP00000509619.1:n.*289G>C
ENST00000687699.1:c.846G>C	ENSP00000508878.1:n.846G>C
ENST00000687786.1:n.2158G>C
ENST00000688100.1:n.1643G>C
ENST00000688588.1:c.722G>C	ENSP00000510802.1:p.Gly241Ala
ENST00000688927.1:n.2933G>C
ENST00000689283.1:c.*385G>C	ENSP00000509050.1:n.*385G>C
ENST00000689477.1:c.*615G>C	ENSP00000508945.1:n.*615G>C
ENST00000689765.1:c.*215G>C	ENSP00000509625.1:n.*215G>C
ENST00000690512.1:c.*573G>C	ENSP00000509793.1:n.*573G>C
ENST00000692039.1:c.*520G>C	ENSP00000508821.1:n.*520G>C
ENST00000692336.1:c.746G>C	ENSP00000508540.1:p.Gly249Ala
ENST00000693133.1:n.1202G>C
ENST00000263578.10:c.722G>C MANE Select	ENSP00000263578.5:p.Gly241Ala
ENST00000263578.9:c.722G>C	ENSP00000263578.5:p.Gly241Ala
ENST00000525083.5:n.442G>C
ENST00000525770.5:c.*354G>C	ENSP00000434739.1:n.*354G>C
ENST00000527004.5:c.*66G>C	ENSP00000436374.1:n.*66G>C
ENST00000530642.1:n.1504G>C
ENST00000532101.5:n.945G>C
ENST00000532125.1:c.680G>C	ENSP00000434178.1:p.Gly227Ala
ENST00000533395.5:n.455G>C
ENST00000533839.5:n.238-377G>C
ENST00000534011.5:n.774G>C
ENST00000534315.5:n.1034G>C
NM_017547.3:c.722G>C	NP_060017.1:p.Gly241Ala
NR_037647.1:n.668G>C
NR_037648.1:n.908G>C
XM_006718879.2:c.212G>C	XP_006718942.1:p.Gly71Ala
XM_006718880.2:c.89G>C	XP_006718943.1:p.Gly30Ala
XM_006718881.2:c.89G>C	XP_006718944.1:p.Gly30Ala
XM_011542895.1:c.212G>C	XP_011541197.1:p.Gly71Ala
XM_011542896.1:c.212G>C	XP_011541198.1:p.Gly71Ala
XM_006718879.3:c.212G>C	XP_006718942.1:p.Gly71Ala
XM_006718881.3:c.89G>C	XP_006718944.1:p.Gly30Ala
XM_011542895.2:c.212G>C	XP_011541197.1:p.Gly71Ala
XM_011542896.2:c.212G>C	XP_011541198.1:p.Gly71Ala
XM_017018000.2:c.722G>C	XP_016873489.1:p.Gly241Ala
XM_017018001.1:c.212G>C	XP_016873490.1:p.Gly71Ala
XM_017018002.1:c.212G>C	XP_016873491.1:p.Gly71Ala
XM_017018003.2:c.89G>C	XP_016873492.1:p.Gly30Ala
XM_017018004.1:c.89G>C	XP_016873493.1:p.Gly30Ala
XM_017018005.1:c.89G>C	XP_016873494.1:p.Gly30Ala
XM_017018006.2:c.89G>C	XP_016873495.1:p.Gly30Ala
NM_017547.4:c.722G>C MANE Select	NP_060017.1:p.Gly241Ala
NR_037647.2:n.554G>C
NR_037648.2:n.899G>C