Canonical Allele Identifier: CA6354128

Gene: FOXRED1

Linked Data

• ClinVar Variation Id: 2047717
• ClinVar RCV Id: RCV002926927
• dbSNP Id: rs760964794
• ExAC: 11:126144823 C / T
• gnomAD v2: 11-126144823-C-T
• gnomAD v4: 11-126274928-C-T
• MyVariant Identifiers: chr11:g.126144823C>T (hg19) ; chr11:g.126274928C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274928C>T , CM000673.2:g.126274928C>T	GRCh38
NC_000011.9:g.126144823C>T , CM000673.1:g.126144823C>T	GRCh37
NC_000011.8:g.125650033C>T	NCBI36
NG_028029.1:g.10889C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.716C>T
ENST00000532101.6:n.734-399C>T
ENST00000532125.2:c.535C>T	ENSP00000434178.2:p.Gln179Ter
ENST00000533839.6:c.86-866C>T	ENSP00000509952.1:n.86-866C>T
ENST00000534011.6:n.833-3C>T
ENST00000685484.1:c.538C>T	ENSP00000510622.1:p.Gln180Ter
ENST00000685601.1:c.538C>T	ENSP00000510603.1:p.Gln180Ter
ENST00000685765.1:c.538C>T	ENSP00000509991.1:p.Gln180Ter
ENST00000685844.1:c.*169-399C>T	ENSP00000509820.1:n.*169-399C>T
ENST00000685857.1:n.972C>T
ENST00000686242.1:c.337C>T	ENSP00000508950.1:n.337C>T
ENST00000686888.1:c.*105C>T	ENSP00000509619.1:n.*105C>T
ENST00000687699.1:c.662C>T	ENSP00000508878.1:n.662C>T
ENST00000687786.1:n.2068-399C>T
ENST00000688100.1:n.1459C>T
ENST00000688588.1:c.538C>T	ENSP00000510802.1:p.Gln180Ter
ENST00000688927.1:n.2444C>T
ENST00000689283.1:c.*201C>T	ENSP00000509050.1:n.*201C>T
ENST00000689477.1:c.*431C>T	ENSP00000508945.1:n.*431C>T
ENST00000689765.1:c.*169-443C>T	ENSP00000509625.1:n.*169-443C>T
ENST00000690512.1:c.*392-3C>T	ENSP00000509793.1:n.*392-3C>T
ENST00000692039.1:c.*336C>T	ENSP00000508821.1:n.*336C>T
ENST00000692336.1:c.562C>T	ENSP00000508540.1:p.Gln188Ter
ENST00000693133.1:n.713C>T
ENST00000263578.10:c.538C>T MANE Select	ENSP00000263578.5:p.Gln180Ter
ENST00000263578.9:c.538C>T	ENSP00000263578.5:p.Gln180Ter
ENST00000524751.5:n.474C>T
ENST00000525083.5:n.352-399C>T
ENST00000525770.5:c.*170C>T	ENSP00000434739.1:n.*170C>T
ENST00000526366.5:n.469C>T
ENST00000527004.5:c.534-399C>T	ENSP00000436374.1:n.534-399C>T
ENST00000527875.1:n.368C>T
ENST00000530642.1:n.1015C>T
ENST00000532101.5:n.761C>T
ENST00000532125.1:c.496C>T	ENSP00000434178.1:p.Gln166Ter
ENST00000533395.5:n.365-399C>T
ENST00000533839.5:n.238-866C>T
ENST00000534011.5:n.593-3C>T
ENST00000534315.5:n.944-399C>T
NM_017547.3:c.538C>T	NP_060017.1:p.Gln180Ter
NR_037647.1:n.484C>T
NR_037648.1:n.724C>T
XM_006718879.2:c.28C>T	XP_006718942.1:p.Gln10Ter
XM_006718880.2:c.-2-399C>T	XP_006718943.1:n.-2-399C>T
XM_006718881.2:c.-2-399C>T	XP_006718944.1:n.-2-399C>T
XM_011542895.1:c.28C>T	XP_011541197.1:p.Gln10Ter
XM_011542896.1:c.28C>T	XP_011541198.1:p.Gln10Ter
XM_006718879.3:c.28C>T	XP_006718942.1:p.Gln10Ter
XM_006718881.3:c.-2-399C>T	XP_006718944.1:n.-2-399C>T
XM_011542895.2:c.28C>T	XP_011541197.1:p.Gln10Ter
XM_011542896.2:c.28C>T	XP_011541198.1:p.Gln10Ter
XM_017018000.2:c.538C>T	XP_016873489.1:p.Gln180Ter
XM_017018001.1:c.28C>T	XP_016873490.1:p.Gln10Ter
XM_017018002.1:c.28C>T	XP_016873491.1:p.Gln10Ter
XM_017018003.2:c.-2-399C>T	XP_016873492.1:n.-2-399C>T
XM_017018004.1:c.-2-399C>T	XP_016873493.1:n.-2-399C>T
XM_017018005.1:c.-2-399C>T	XP_016873494.1:n.-2-399C>T
XM_017018006.2:c.-2-399C>T	XP_016873495.1:n.-2-399C>T
NM_017547.4:c.538C>T MANE Select	NP_060017.1:p.Gln180Ter
NR_037647.2:n.370C>T
NR_037648.2:n.715C>T