Canonical Allele Identifier: CA477516097

Gene: FOXRED1

Linked Data

• ClinVar Variation Id: 2825876
• ClinVar RCV Id: RCV003681173
• dbSNP Id: rs1376033076
• MyVariant Identifiers: chr11:g.126145292G>A (hg19) ; chr11:g.126275397G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275397G>A , CM000673.2:g.126275397G>A	GRCh38
NC_000011.9:g.126145292G>A , CM000673.1:g.126145292G>A	GRCh37
NC_000011.8:g.125650502G>A	NCBI36
NG_028029.1:g.11358G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1185G>A
ENST00000532101.6:n.804G>A
ENST00000532125.2:c.699G>A	ENSP00000434178.2:p.Leu233=
ENST00000533839.6:c.86-397G>A	ENSP00000509952.1:n.86-397G>A
ENST00000534011.6:n.994G>A
ENST00000685484.1:c.702G>A	ENSP00000510622.1:p.Leu234=
ENST00000685601.1:c.702G>A	ENSP00000510603.1:p.Leu234=
ENST00000685765.1:c.702G>A	ENSP00000509991.1:p.Leu234=
ENST00000685844.1:c.*239G>A	ENSP00000509820.1:n.*239G>A
ENST00000685857.1:n.1441G>A
ENST00000686242.1:c.501G>A	ENSP00000508950.1:n.501G>A
ENST00000686888.1:c.*269G>A	ENSP00000509619.1:n.*269G>A
ENST00000687699.1:c.826G>A	ENSP00000508878.1:n.826G>A
ENST00000687786.1:n.2138G>A
ENST00000688100.1:n.1623G>A
ENST00000688588.1:c.702G>A	ENSP00000510802.1:p.Leu234=
ENST00000688927.1:n.2913G>A
ENST00000689283.1:c.*365G>A	ENSP00000509050.1:n.*365G>A
ENST00000689477.1:c.*595G>A	ENSP00000508945.1:n.*595G>A
ENST00000689765.1:c.*195G>A	ENSP00000509625.1:n.*195G>A
ENST00000690512.1:c.*553G>A	ENSP00000509793.1:n.*553G>A
ENST00000692039.1:c.*500G>A	ENSP00000508821.1:n.*500G>A
ENST00000692336.1:c.726G>A	ENSP00000508540.1:p.Leu242=
ENST00000693133.1:n.1182G>A
ENST00000263578.10:c.702G>A MANE Select	ENSP00000263578.5:p.Leu234=
ENST00000263578.9:c.702G>A	ENSP00000263578.5:p.Leu234=
ENST00000525083.5:n.422G>A
ENST00000525770.5:c.*334G>A	ENSP00000434739.1:n.*334G>A
ENST00000527004.5:c.*46G>A	ENSP00000436374.1:n.*46G>A
ENST00000530642.1:n.1484G>A
ENST00000532101.5:n.925G>A
ENST00000532125.1:c.660G>A	ENSP00000434178.1:p.Leu220=
ENST00000533395.5:n.435G>A
ENST00000533839.5:n.238-397G>A
ENST00000534011.5:n.754G>A
ENST00000534315.5:n.1014G>A
NM_017547.3:c.702G>A	NP_060017.1:p.Leu234=
NR_037647.1:n.648G>A
NR_037648.1:n.888G>A
XM_006718879.2:c.192G>A	XP_006718942.1:p.Leu64=
XM_006718880.2:c.69G>A	XP_006718943.1:p.Leu23=
XM_006718881.2:c.69G>A	XP_006718944.1:p.Leu23=
XM_011542895.1:c.192G>A	XP_011541197.1:p.Leu64=
XM_011542896.1:c.192G>A	XP_011541198.1:p.Leu64=
XM_006718879.3:c.192G>A	XP_006718942.1:p.Leu64=
XM_006718881.3:c.69G>A	XP_006718944.1:p.Leu23=
XM_011542895.2:c.192G>A	XP_011541197.1:p.Leu64=
XM_011542896.2:c.192G>A	XP_011541198.1:p.Leu64=
XM_017018000.2:c.702G>A	XP_016873489.1:p.Leu234=
XM_017018001.1:c.192G>A	XP_016873490.1:p.Leu64=
XM_017018002.1:c.192G>A	XP_016873491.1:p.Leu64=
XM_017018003.2:c.69G>A	XP_016873492.1:p.Leu23=
XM_017018004.1:c.69G>A	XP_016873493.1:p.Leu23=
XM_017018005.1:c.69G>A	XP_016873494.1:p.Leu23=
XM_017018006.2:c.69G>A	XP_016873495.1:p.Leu23=
NM_017547.4:c.702G>A MANE Select	NP_060017.1:p.Leu234=
NR_037647.2:n.534G>A
NR_037648.2:n.879G>A