Canonical Allele Identifier: CA383230240

Gene: FOXRED1

Linked Data

• dbSNP Id: rs1197069497
• gnomAD v2: 11-126145303-T-C
• gnomAD v4: 11-126275408-T-C
• MyVariant Identifiers: chr11:g.126145303T>C (hg19) ; chr11:g.126275408T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275408T>C , CM000673.2:g.126275408T>C	GRCh38
NC_000011.9:g.126145303T>C , CM000673.1:g.126145303T>C	GRCh37
NC_000011.8:g.125650513T>C	NCBI36
NG_028029.1:g.11369T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1196T>C
ENST00000532101.6:n.815T>C
ENST00000532125.2:c.710T>C	ENSP00000434178.2:p.Phe237Ser
ENST00000533839.6:c.86-386T>C	ENSP00000509952.1:n.86-386T>C
ENST00000534011.6:n.1005T>C
ENST00000685484.1:c.713T>C	ENSP00000510622.1:p.Phe238Ser
ENST00000685601.1:c.713T>C	ENSP00000510603.1:p.Phe238Ser
ENST00000685765.1:c.713T>C	ENSP00000509991.1:p.Phe238Ser
ENST00000685844.1:c.*250T>C	ENSP00000509820.1:n.*250T>C
ENST00000685857.1:n.1452T>C
ENST00000686242.1:c.512T>C	ENSP00000508950.1:n.512T>C
ENST00000686888.1:c.*280T>C	ENSP00000509619.1:n.*280T>C
ENST00000687699.1:c.837T>C	ENSP00000508878.1:n.837T>C
ENST00000687786.1:n.2149T>C
ENST00000688100.1:n.1634T>C
ENST00000688588.1:c.713T>C	ENSP00000510802.1:p.Phe238Ser
ENST00000688927.1:n.2924T>C
ENST00000689283.1:c.*376T>C	ENSP00000509050.1:n.*376T>C
ENST00000689477.1:c.*606T>C	ENSP00000508945.1:n.*606T>C
ENST00000689765.1:c.*206T>C	ENSP00000509625.1:n.*206T>C
ENST00000690512.1:c.*564T>C	ENSP00000509793.1:n.*564T>C
ENST00000692039.1:c.*511T>C	ENSP00000508821.1:n.*511T>C
ENST00000692336.1:c.737T>C	ENSP00000508540.1:p.Phe246Ser
ENST00000693133.1:n.1193T>C
ENST00000263578.10:c.713T>C MANE Select	ENSP00000263578.5:p.Phe238Ser
ENST00000263578.9:c.713T>C	ENSP00000263578.5:p.Phe238Ser
ENST00000525083.5:n.433T>C
ENST00000525770.5:c.*345T>C	ENSP00000434739.1:n.*345T>C
ENST00000527004.5:c.*57T>C	ENSP00000436374.1:n.*57T>C
ENST00000530642.1:n.1495T>C
ENST00000532101.5:n.936T>C
ENST00000532125.1:c.671T>C	ENSP00000434178.1:p.Phe224Ser
ENST00000533395.5:n.446T>C
ENST00000533839.5:n.238-386T>C
ENST00000534011.5:n.765T>C
ENST00000534315.5:n.1025T>C
NM_017547.3:c.713T>C	NP_060017.1:p.Phe238Ser
NR_037647.1:n.659T>C
NR_037648.1:n.899T>C
XM_006718879.2:c.203T>C	XP_006718942.1:p.Phe68Ser
XM_006718880.2:c.80T>C	XP_006718943.1:p.Phe27Ser
XM_006718881.2:c.80T>C	XP_006718944.1:p.Phe27Ser
XM_011542895.1:c.203T>C	XP_011541197.1:p.Phe68Ser
XM_011542896.1:c.203T>C	XP_011541198.1:p.Phe68Ser
XM_006718879.3:c.203T>C	XP_006718942.1:p.Phe68Ser
XM_006718881.3:c.80T>C	XP_006718944.1:p.Phe27Ser
XM_011542895.2:c.203T>C	XP_011541197.1:p.Phe68Ser
XM_011542896.2:c.203T>C	XP_011541198.1:p.Phe68Ser
XM_017018000.2:c.713T>C	XP_016873489.1:p.Phe238Ser
XM_017018001.1:c.203T>C	XP_016873490.1:p.Phe68Ser
XM_017018002.1:c.203T>C	XP_016873491.1:p.Phe68Ser
XM_017018003.2:c.80T>C	XP_016873492.1:p.Phe27Ser
XM_017018004.1:c.80T>C	XP_016873493.1:p.Phe27Ser
XM_017018005.1:c.80T>C	XP_016873494.1:p.Phe27Ser
XM_017018006.2:c.80T>C	XP_016873495.1:p.Phe27Ser
NM_017547.4:c.713T>C MANE Select	NP_060017.1:p.Phe238Ser
NR_037647.2:n.545T>C
NR_037648.2:n.890T>C