Canonical Allele Identifier: CA6354149

Gene: FOXRED1

Linked Data

• dbSNP Id: rs770426760
• ExAC: 11:126144941 A / G
• gnomAD v2: 11-126144941-A-G
• gnomAD v3: 11-126275046-A-G
• gnomAD v4: 11-126275046-A-G
• MyVariant Identifiers: chr11:g.126144941A>G (hg19) ; chr11:g.126275046A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275046A>G , CM000673.2:g.126275046A>G	GRCh38
NC_000011.9:g.126144941A>G , CM000673.1:g.126144941A>G	GRCh37
NC_000011.8:g.125650151A>G	NCBI36
NG_028029.1:g.11007A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.834A>G
ENST00000532101.6:n.734-281A>G
ENST00000532125.2:c.628+25A>G	ENSP00000434178.2:n.628+25A>G
ENST00000533839.6:c.86-748A>G	ENSP00000509952.1:n.86-748A>G
ENST00000534011.6:n.923+25A>G
ENST00000685484.1:c.631+25A>G	ENSP00000510622.1:n.631+25A>G
ENST00000685601.1:c.631+25A>G	ENSP00000510603.1:n.631+25A>G
ENST00000685765.1:c.631+25A>G	ENSP00000509991.1:n.631+25A>G
ENST00000685844.1:c.*169-281A>G	ENSP00000509820.1:n.*169-281A>G
ENST00000685857.1:n.1090A>G
ENST00000686242.1:c.430+25A>G	ENSP00000508950.1:n.430+25A>G
ENST00000686888.1:c.*198+25A>G	ENSP00000509619.1:n.*198+25A>G
ENST00000687699.1:c.755+25A>G	ENSP00000508878.1:n.755+25A>G
ENST00000687786.1:n.2068-281A>G
ENST00000688100.1:n.1552+25A>G
ENST00000688588.1:c.631+25A>G	ENSP00000510802.1:n.631+25A>G
ENST00000688927.1:n.2562A>G
ENST00000689283.1:c.*294+25A>G	ENSP00000509050.1:n.*294+25A>G
ENST00000689477.1:c.*524+25A>G	ENSP00000508945.1:n.*524+25A>G
ENST00000689765.1:c.*169-325A>G	ENSP00000509625.1:n.*169-325A>G
ENST00000690512.1:c.*482+25A>G	ENSP00000509793.1:n.*482+25A>G
ENST00000692039.1:c.*429+25A>G	ENSP00000508821.1:n.*429+25A>G
ENST00000692336.1:c.655+25A>G	ENSP00000508540.1:n.655+25A>G
ENST00000693133.1:n.831A>G
ENST00000263578.10:c.631+25A>G MANE Select	ENSP00000263578.5:n.631+25A>G
ENST00000263578.9:c.631+25A>G	ENSP00000263578.5:n.631+25A>G
ENST00000524751.5:n.592A>G
ENST00000525083.5:n.352-281A>G
ENST00000525770.5:c.*263+25A>G	ENSP00000434739.1:n.*263+25A>G
ENST00000527004.5:c.534-281A>G	ENSP00000436374.1:n.534-281A>G
ENST00000527875.1:n.486A>G
ENST00000530642.1:n.1133A>G
ENST00000532101.5:n.854+25A>G
ENST00000532125.1:c.589+25A>G	ENSP00000434178.1:n.589+25A>G
ENST00000533395.5:n.365-281A>G
ENST00000533839.5:n.238-748A>G
ENST00000534011.5:n.683+25A>G
ENST00000534315.5:n.944-281A>G
NM_017547.3:c.631+25A>G	NP_060017.1:n.631+25A>G
NR_037647.1:n.577+25A>G
NR_037648.1:n.817+25A>G
XM_006718879.2:c.121+25A>G	XP_006718942.1:n.121+25A>G
XM_006718880.2:c.-2-281A>G	XP_006718943.1:n.-2-281A>G
XM_006718881.2:c.-2-281A>G	XP_006718944.1:n.-2-281A>G
XM_011542895.1:c.121+25A>G	XP_011541197.1:n.121+25A>G
XM_011542896.1:c.121+25A>G	XP_011541198.1:n.121+25A>G
XM_006718879.3:c.121+25A>G	XP_006718942.1:n.121+25A>G
XM_006718881.3:c.-2-281A>G	XP_006718944.1:n.-2-281A>G
XM_011542895.2:c.121+25A>G	XP_011541197.1:n.121+25A>G
XM_011542896.2:c.121+25A>G	XP_011541198.1:n.121+25A>G
XM_017018000.2:c.631+25A>G	XP_016873489.1:n.631+25A>G
XM_017018001.1:c.121+25A>G	XP_016873490.1:n.121+25A>G
XM_017018002.1:c.121+25A>G	XP_016873491.1:n.121+25A>G
XM_017018003.2:c.-2-281A>G	XP_016873492.1:n.-2-281A>G
XM_017018004.1:c.-2-281A>G	XP_016873493.1:n.-2-281A>G
XM_017018005.1:c.-2-281A>G	XP_016873494.1:n.-2-281A>G
XM_017018006.2:c.-2-281A>G	XP_016873495.1:n.-2-281A>G
NM_017547.4:c.631+25A>G MANE Select	NP_060017.1:n.631+25A>G
NR_037647.2:n.463+25A>G
NR_037648.2:n.808+25A>G