Canonical Allele Identifier: CA383229167

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126141472T>G (hg19) ; chr11:g.126271577T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126271577T>G , CM000673.2:g.126271577T>G	GRCh38
NC_000011.9:g.126141472T>G , CM000673.1:g.126141472T>G	GRCh37
NC_000011.8:g.125646682T>G	NCBI36
NG_028029.1:g.7538T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.404T>G
ENST00000532101.6:n.403T>G
ENST00000532125.2:c.226T>G	ENSP00000434178.2:p.Leu76Val
ENST00000533839.6:c.85+2286T>G	ENSP00000509952.1:n.85+2286T>G
ENST00000534011.6:n.502T>G
ENST00000685484.1:c.226T>G	ENSP00000510622.1:p.Leu76Val
ENST00000685601.1:c.226T>G	ENSP00000510603.1:p.Leu76Val
ENST00000685765.1:c.226T>G	ENSP00000509991.1:p.Leu76Val
ENST00000685844.1:c.86-1392T>G	ENSP00000509820.1:n.86-1392T>G
ENST00000685857.1:n.404T>G
ENST00000686242.1:c.86-1392T>G	ENSP00000508950.1:n.86-1392T>G
ENST00000686888.1:c.226T>G	ENSP00000509619.1:p.Leu76Val
ENST00000687699.1:c.350T>G	ENSP00000508878.1:n.350T>G
ENST00000687786.1:n.1559T>G
ENST00000688588.1:c.226T>G	ENSP00000510802.1:p.Leu76Val
ENST00000688927.1:n.404T>G
ENST00000689283.1:c.210-1392T>G	ENSP00000509050.1:n.210-1392T>G
ENST00000689477.1:c.*119T>G	ENSP00000508945.1:n.*119T>G
ENST00000689765.1:c.86-1392T>G	ENSP00000509625.1:n.86-1392T>G
ENST00000690512.1:c.86-901T>G	ENSP00000509793.1:n.86-901T>G
ENST00000692039.1:c.*24T>G	ENSP00000508821.1:n.*24T>G
ENST00000692336.1:c.226T>G	ENSP00000508540.1:p.Leu76Val
ENST00000693133.1:n.226-1392T>G
ENST00000263578.10:c.226T>G MANE Select	ENSP00000263578.5:p.Leu76Val
ENST00000263578.9:c.226T>G	ENSP00000263578.5:p.Leu76Val
ENST00000524751.5:n.223-1392T>G
ENST00000525083.5:n.122-1392T>G
ENST00000525770.5:c.86-1392T>G	ENSP00000434739.1:n.86-1392T>G
ENST00000526366.5:n.101-142T>G
ENST00000526525.1:n.246-1392T>G
ENST00000527004.5:c.226T>G	ENSP00000436374.1:p.Leu76Val
ENST00000529802.1:n.276T>G
ENST00000532101.5:n.449T>G
ENST00000532125.1:c.184T>G	ENSP00000434178.1:p.Leu62Val
ENST00000533839.5:n.237+2286T>G
ENST00000534011.5:n.158-901T>G
ENST00000534315.5:n.633T>G
NM_017547.3:c.226T>G	NP_060017.1:p.Leu76Val
NR_037647.1:n.253-1392T>G
NR_037648.1:n.412T>G
XM_006718880.2:c.-313T>G	XP_006718943.1:n.-313T>G
XM_006718881.2:c.-232-1392T>G	XP_006718944.1:n.-232-1392T>G
XM_011542895.1:c.-285T>G	XP_011541197.1:n.-285T>G
XM_011542896.1:c.-305T>G	XP_011541198.1:n.-305T>G
XM_006718881.3:c.-232-1392T>G	XP_006718944.1:n.-232-1392T>G
XM_011542895.2:c.-285T>G	XP_011541197.1:n.-285T>G
XM_011542896.2:c.-305T>G	XP_011541198.1:n.-305T>G
XM_017018000.2:c.226T>G	XP_016873489.1:p.Leu76Val
XM_017018001.1:c.-305T>G	XP_016873490.1:n.-305T>G
XM_017018002.1:c.-224-1392T>G	XP_016873491.1:n.-224-1392T>G
XM_017018003.2:c.-313T>G	XP_016873492.1:n.-313T>G
XM_017018004.1:c.-313T>G	XP_016873493.1:n.-313T>G
XM_017018005.1:c.-511T>G	XP_016873494.1:n.-511T>G
XM_017018006.2:c.-313T>G	XP_016873495.1:n.-313T>G
NM_017547.4:c.226T>G MANE Select	NP_060017.1:p.Leu76Val
NR_037647.2:n.139-1392T>G
NR_037648.2:n.403T>G