Canonical Allele Identifier: CA383230178

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145269C>G (hg19) ; chr11:g.126275374C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275374C>G , CM000673.2:g.126275374C>G	GRCh38
NC_000011.9:g.126145269C>G , CM000673.1:g.126145269C>G	GRCh37
NC_000011.8:g.125650479C>G	NCBI36
NG_028029.1:g.11335C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1162C>G
ENST00000532101.6:n.781C>G
ENST00000532125.2:c.676C>G	ENSP00000434178.2:p.Leu226Val
ENST00000533839.6:c.86-420C>G	ENSP00000509952.1:n.86-420C>G
ENST00000534011.6:n.971C>G
ENST00000685484.1:c.679C>G	ENSP00000510622.1:p.Leu227Val
ENST00000685601.1:c.679C>G	ENSP00000510603.1:p.Leu227Val
ENST00000685765.1:c.679C>G	ENSP00000509991.1:p.Leu227Val
ENST00000685844.1:c.*216C>G	ENSP00000509820.1:n.*216C>G
ENST00000685857.1:n.1418C>G
ENST00000686242.1:c.478C>G	ENSP00000508950.1:n.478C>G
ENST00000686888.1:c.*246C>G	ENSP00000509619.1:n.*246C>G
ENST00000687699.1:c.803C>G	ENSP00000508878.1:n.803C>G
ENST00000687786.1:n.2115C>G
ENST00000688100.1:n.1600C>G
ENST00000688588.1:c.679C>G	ENSP00000510802.1:p.Leu227Val
ENST00000688927.1:n.2890C>G
ENST00000689283.1:c.*342C>G	ENSP00000509050.1:n.*342C>G
ENST00000689477.1:c.*572C>G	ENSP00000508945.1:n.*572C>G
ENST00000689765.1:c.*172C>G	ENSP00000509625.1:n.*172C>G
ENST00000690512.1:c.*530C>G	ENSP00000509793.1:n.*530C>G
ENST00000692039.1:c.*477C>G	ENSP00000508821.1:n.*477C>G
ENST00000692336.1:c.703C>G	ENSP00000508540.1:p.Leu235Val
ENST00000693133.1:n.1159C>G
ENST00000263578.10:c.679C>G MANE Select	ENSP00000263578.5:p.Leu227Val
ENST00000263578.9:c.679C>G	ENSP00000263578.5:p.Leu227Val
ENST00000525083.5:n.399C>G
ENST00000525770.5:c.*311C>G	ENSP00000434739.1:n.*311C>G
ENST00000527004.5:c.*23C>G	ENSP00000436374.1:n.*23C>G
ENST00000530642.1:n.1461C>G
ENST00000532101.5:n.902C>G
ENST00000532125.1:c.637C>G	ENSP00000434178.1:p.Leu213Val
ENST00000533395.5:n.412C>G
ENST00000533839.5:n.238-420C>G
ENST00000534011.5:n.731C>G
ENST00000534315.5:n.991C>G
NM_017547.3:c.679C>G	NP_060017.1:p.Leu227Val
NR_037647.1:n.625C>G
NR_037648.1:n.865C>G
XM_006718879.2:c.169C>G	XP_006718942.1:p.Leu57Val
XM_006718880.2:c.46C>G	XP_006718943.1:p.Leu16Val
XM_006718881.2:c.46C>G	XP_006718944.1:p.Leu16Val
XM_011542895.1:c.169C>G	XP_011541197.1:p.Leu57Val
XM_011542896.1:c.169C>G	XP_011541198.1:p.Leu57Val
XM_006718879.3:c.169C>G	XP_006718942.1:p.Leu57Val
XM_006718881.3:c.46C>G	XP_006718944.1:p.Leu16Val
XM_011542895.2:c.169C>G	XP_011541197.1:p.Leu57Val
XM_011542896.2:c.169C>G	XP_011541198.1:p.Leu57Val
XM_017018000.2:c.679C>G	XP_016873489.1:p.Leu227Val
XM_017018001.1:c.169C>G	XP_016873490.1:p.Leu57Val
XM_017018002.1:c.169C>G	XP_016873491.1:p.Leu57Val
XM_017018003.2:c.46C>G	XP_016873492.1:p.Leu16Val
XM_017018004.1:c.46C>G	XP_016873493.1:p.Leu16Val
XM_017018005.1:c.46C>G	XP_016873494.1:p.Leu16Val
XM_017018006.2:c.46C>G	XP_016873495.1:p.Leu16Val
NM_017547.4:c.679C>G MANE Select	NP_060017.1:p.Leu227Val
NR_037647.2:n.511C>G
NR_037648.2:n.856C>G