Canonical Allele Identifier: CA383230237

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145302T>C (hg19) ; chr11:g.126275407T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275407T>C , CM000673.2:g.126275407T>C	GRCh38
NC_000011.9:g.126145302T>C , CM000673.1:g.126145302T>C	GRCh37
NC_000011.8:g.125650512T>C	NCBI36
NG_028029.1:g.11368T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1195T>C
ENST00000532101.6:n.814T>C
ENST00000532125.2:c.709T>C	ENSP00000434178.2:p.Phe237Leu
ENST00000533839.6:c.86-387T>C	ENSP00000509952.1:n.86-387T>C
ENST00000534011.6:n.1004T>C
ENST00000685484.1:c.712T>C	ENSP00000510622.1:p.Phe238Leu
ENST00000685601.1:c.712T>C	ENSP00000510603.1:p.Phe238Leu
ENST00000685765.1:c.712T>C	ENSP00000509991.1:p.Phe238Leu
ENST00000685844.1:c.*249T>C	ENSP00000509820.1:n.*249T>C
ENST00000685857.1:n.1451T>C
ENST00000686242.1:c.511T>C	ENSP00000508950.1:n.511T>C
ENST00000686888.1:c.*279T>C	ENSP00000509619.1:n.*279T>C
ENST00000687699.1:c.836T>C	ENSP00000508878.1:n.836T>C
ENST00000687786.1:n.2148T>C
ENST00000688100.1:n.1633T>C
ENST00000688588.1:c.712T>C	ENSP00000510802.1:p.Phe238Leu
ENST00000688927.1:n.2923T>C
ENST00000689283.1:c.*375T>C	ENSP00000509050.1:n.*375T>C
ENST00000689477.1:c.*605T>C	ENSP00000508945.1:n.*605T>C
ENST00000689765.1:c.*205T>C	ENSP00000509625.1:n.*205T>C
ENST00000690512.1:c.*563T>C	ENSP00000509793.1:n.*563T>C
ENST00000692039.1:c.*510T>C	ENSP00000508821.1:n.*510T>C
ENST00000692336.1:c.736T>C	ENSP00000508540.1:p.Phe246Leu
ENST00000693133.1:n.1192T>C
ENST00000263578.10:c.712T>C MANE Select	ENSP00000263578.5:p.Phe238Leu
ENST00000263578.9:c.712T>C	ENSP00000263578.5:p.Phe238Leu
ENST00000525083.5:n.432T>C
ENST00000525770.5:c.*344T>C	ENSP00000434739.1:n.*344T>C
ENST00000527004.5:c.*56T>C	ENSP00000436374.1:n.*56T>C
ENST00000530642.1:n.1494T>C
ENST00000532101.5:n.935T>C
ENST00000532125.1:c.670T>C	ENSP00000434178.1:p.Phe224Leu
ENST00000533395.5:n.445T>C
ENST00000533839.5:n.238-387T>C
ENST00000534011.5:n.764T>C
ENST00000534315.5:n.1024T>C
NM_017547.3:c.712T>C	NP_060017.1:p.Phe238Leu
NR_037647.1:n.658T>C
NR_037648.1:n.898T>C
XM_006718879.2:c.202T>C	XP_006718942.1:p.Phe68Leu
XM_006718880.2:c.79T>C	XP_006718943.1:p.Phe27Leu
XM_006718881.2:c.79T>C	XP_006718944.1:p.Phe27Leu
XM_011542895.1:c.202T>C	XP_011541197.1:p.Phe68Leu
XM_011542896.1:c.202T>C	XP_011541198.1:p.Phe68Leu
XM_006718879.3:c.202T>C	XP_006718942.1:p.Phe68Leu
XM_006718881.3:c.79T>C	XP_006718944.1:p.Phe27Leu
XM_011542895.2:c.202T>C	XP_011541197.1:p.Phe68Leu
XM_011542896.2:c.202T>C	XP_011541198.1:p.Phe68Leu
XM_017018000.2:c.712T>C	XP_016873489.1:p.Phe238Leu
XM_017018001.1:c.202T>C	XP_016873490.1:p.Phe68Leu
XM_017018002.1:c.202T>C	XP_016873491.1:p.Phe68Leu
XM_017018003.2:c.79T>C	XP_016873492.1:p.Phe27Leu
XM_017018004.1:c.79T>C	XP_016873493.1:p.Phe27Leu
XM_017018005.1:c.79T>C	XP_016873494.1:p.Phe27Leu
XM_017018006.2:c.79T>C	XP_016873495.1:p.Phe27Leu
NM_017547.4:c.712T>C MANE Select	NP_060017.1:p.Phe238Leu
NR_037647.2:n.544T>C
NR_037648.2:n.889T>C