Canonical Allele Identifier: CA383230251

Gene: FOXRED1

Linked Data

• dbSNP Id: rs1377098439
• gnomAD v2: 11-126145307-C-G
• MyVariant Identifiers: chr11:g.126145307C>G (hg19) ; chr11:g.126275412C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275412C>G , CM000673.2:g.126275412C>G	GRCh38
NC_000011.9:g.126145307C>G , CM000673.1:g.126145307C>G	GRCh37
NC_000011.8:g.125650517C>G	NCBI36
NG_028029.1:g.11373C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1200C>G
ENST00000532101.6:n.819C>G
ENST00000532125.2:c.714C>G	ENSP00000434178.2:p.Cys238Trp
ENST00000533839.6:c.86-382C>G	ENSP00000509952.1:n.86-382C>G
ENST00000534011.6:n.1009C>G
ENST00000685484.1:c.717C>G	ENSP00000510622.1:p.Cys239Trp
ENST00000685601.1:c.717C>G	ENSP00000510603.1:p.Cys239Trp
ENST00000685765.1:c.717C>G	ENSP00000509991.1:p.Cys239Trp
ENST00000685844.1:c.*254C>G	ENSP00000509820.1:n.*254C>G
ENST00000685857.1:n.1456C>G
ENST00000686242.1:c.516C>G	ENSP00000508950.1:n.516C>G
ENST00000686888.1:c.*284C>G	ENSP00000509619.1:n.*284C>G
ENST00000687699.1:c.841C>G	ENSP00000508878.1:n.841C>G
ENST00000687786.1:n.2153C>G
ENST00000688100.1:n.1638C>G
ENST00000688588.1:c.717C>G	ENSP00000510802.1:p.Cys239Trp
ENST00000688927.1:n.2928C>G
ENST00000689283.1:c.*380C>G	ENSP00000509050.1:n.*380C>G
ENST00000689477.1:c.*610C>G	ENSP00000508945.1:n.*610C>G
ENST00000689765.1:c.*210C>G	ENSP00000509625.1:n.*210C>G
ENST00000690512.1:c.*568C>G	ENSP00000509793.1:n.*568C>G
ENST00000692039.1:c.*515C>G	ENSP00000508821.1:n.*515C>G
ENST00000692336.1:c.741C>G	ENSP00000508540.1:p.Cys247Trp
ENST00000693133.1:n.1197C>G
ENST00000263578.10:c.717C>G MANE Select	ENSP00000263578.5:p.Cys239Trp
ENST00000263578.9:c.717C>G	ENSP00000263578.5:p.Cys239Trp
ENST00000525083.5:n.437C>G
ENST00000525770.5:c.*349C>G	ENSP00000434739.1:n.*349C>G
ENST00000527004.5:c.*61C>G	ENSP00000436374.1:n.*61C>G
ENST00000530642.1:n.1499C>G
ENST00000532101.5:n.940C>G
ENST00000532125.1:c.675C>G	ENSP00000434178.1:p.Cys225Trp
ENST00000533395.5:n.450C>G
ENST00000533839.5:n.238-382C>G
ENST00000534011.5:n.769C>G
ENST00000534315.5:n.1029C>G
NM_017547.3:c.717C>G	NP_060017.1:p.Cys239Trp
NR_037647.1:n.663C>G
NR_037648.1:n.903C>G
XM_006718879.2:c.207C>G	XP_006718942.1:p.Cys69Trp
XM_006718880.2:c.84C>G	XP_006718943.1:p.Cys28Trp
XM_006718881.2:c.84C>G	XP_006718944.1:p.Cys28Trp
XM_011542895.1:c.207C>G	XP_011541197.1:p.Cys69Trp
XM_011542896.1:c.207C>G	XP_011541198.1:p.Cys69Trp
XM_006718879.3:c.207C>G	XP_006718942.1:p.Cys69Trp
XM_006718881.3:c.84C>G	XP_006718944.1:p.Cys28Trp
XM_011542895.2:c.207C>G	XP_011541197.1:p.Cys69Trp
XM_011542896.2:c.207C>G	XP_011541198.1:p.Cys69Trp
XM_017018000.2:c.717C>G	XP_016873489.1:p.Cys239Trp
XM_017018001.1:c.207C>G	XP_016873490.1:p.Cys69Trp
XM_017018002.1:c.207C>G	XP_016873491.1:p.Cys69Trp
XM_017018003.2:c.84C>G	XP_016873492.1:p.Cys28Trp
XM_017018004.1:c.84C>G	XP_016873493.1:p.Cys28Trp
XM_017018005.1:c.84C>G	XP_016873494.1:p.Cys28Trp
XM_017018006.2:c.84C>G	XP_016873495.1:p.Cys28Trp
NM_017547.4:c.717C>G MANE Select	NP_060017.1:p.Cys239Trp
NR_037647.2:n.549C>G
NR_037648.2:n.894C>G