Canonical Allele Identifier: CA113794

Gene: FOXRED1

Linked Data

• ClinVar Variation Id: 6
• ClinVar RCV Id: RCV000000016
• dbSNP Id: rs267606830
• gnomAD v4: 11-126277517-A-G
• MyVariant Identifiers: chr11:g.126147412A>G (hg19) ; chr11:g.126277517A>G (hg38)
• PubMed: PMID:20818383

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126277517A>G , CM000673.2:g.126277517A>G	GRCh38
NC_000011.9:g.126147412A>G , CM000673.1:g.126147412A>G	GRCh37
NC_000011.8:g.125652622A>G	NCBI36
NG_028029.1:g.13478A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1772A>G
ENST00000532101.6:n.1418A>G
ENST00000532125.2:c.1286A>G	ENSP00000434178.2:p.Asn429Ser
ENST00000533839.6:c.641A>G	ENSP00000509952.1:p.Asn214Ser
ENST00000534011.6:n.1522A>G
ENST00000685484.1:c.*285A>G	ENSP00000510622.1:n.*285A>G
ENST00000685601.1:c.*341A>G	ENSP00000510603.1:n.*341A>G
ENST00000685765.1:c.*277A>G	ENSP00000509991.1:n.*277A>G
ENST00000685844.1:c.*899A>G	ENSP00000509820.1:n.*899A>G
ENST00000685857.1:n.2393A>G
ENST00000686242.1:c.1088A>G	ENSP00000508950.1:n.1088A>G
ENST00000686888.1:c.*856A>G	ENSP00000509619.1:n.*856A>G
ENST00000687699.1:c.1413A>G	ENSP00000508878.1:n.1413A>G
ENST00000687786.1:n.2725A>G
ENST00000688100.1:n.2182A>G
ENST00000688588.1:c.*109A>G	ENSP00000510802.1:n.*109A>G
ENST00000688927.1:n.3500A>G
ENST00000689283.1:c.*952A>G	ENSP00000509050.1:n.*952A>G
ENST00000689477.1:c.*1182A>G	ENSP00000508945.1:n.*1182A>G
ENST00000689765.1:c.*782A>G	ENSP00000509625.1:n.*782A>G
ENST00000690512.1:c.*1140A>G	ENSP00000509793.1:n.*1140A>G
ENST00000692039.1:c.*1114A>G	ENSP00000508821.1:n.*1114A>G
ENST00000692336.1:c.1313A>G	ENSP00000508540.1:p.Asn438Ser
ENST00000693133.1:n.2134A>G
ENST00000263578.10:c.1289A>G MANE Select	ENSP00000263578.5:p.Asn430Ser
ENST00000263578.9:c.1289A>G	ENSP00000263578.5:p.Asn430Ser
ENST00000525083.5:n.1082A>G
ENST00000525770.5:c.*921A>G	ENSP00000434739.1:n.*921A>G
ENST00000527004.5:c.*633A>G	ENSP00000436374.1:n.*633A>G
ENST00000530642.1:n.2436A>G
ENST00000532125.1:c.1247A>G	ENSP00000434178.1:p.Asn416Ser
ENST00000532590.1:n.347A>G
ENST00000534011.5:n.1341A>G
ENST00000534315.5:n.1601A>G
NM_017547.3:c.1289A>G	NP_060017.1:p.Asn430Ser
NR_037647.1:n.1235A>G
NR_037648.1:n.1475A>G
XM_006718879.2:c.779A>G	XP_006718942.1:p.Asn260Ser
XM_006718880.2:c.656A>G	XP_006718943.1:p.Asn219Ser
XM_006718881.2:c.656A>G	XP_006718944.1:p.Asn219Ser
XM_011542895.1:c.779A>G	XP_011541197.1:p.Asn260Ser
XM_011542896.1:c.779A>G	XP_011541198.1:p.Asn260Ser
XM_006718879.3:c.779A>G	XP_006718942.1:p.Asn260Ser
XM_006718881.3:c.656A>G	XP_006718944.1:p.Asn219Ser
XM_011542895.2:c.779A>G	XP_011541197.1:p.Asn260Ser
XM_011542896.2:c.779A>G	XP_011541198.1:p.Asn260Ser
XM_017018000.2:c.1286A>G	XP_016873489.1:p.Asn429Ser
XM_017018001.1:c.779A>G	XP_016873490.1:p.Asn260Ser
XM_017018002.1:c.779A>G	XP_016873491.1:p.Asn260Ser
XM_017018003.2:c.656A>G	XP_016873492.1:p.Asn219Ser
XM_017018004.1:c.656A>G	XP_016873493.1:p.Asn219Ser
XM_017018005.1:c.656A>G	XP_016873494.1:p.Asn219Ser
XM_017018006.2:c.653A>G	XP_016873495.1:p.Asn218Ser
NM_017547.4:c.1289A>G MANE Select	NP_060017.1:p.Asn430Ser
NR_037647.2:n.1121A>G
NR_037648.2:n.1466A>G