Canonical Allele Identifier: CA383230209

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145287T>G (hg19) ; chr11:g.126275392T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275392T>G , CM000673.2:g.126275392T>G	GRCh38
NC_000011.9:g.126145287T>G , CM000673.1:g.126145287T>G	GRCh37
NC_000011.8:g.125650497T>G	NCBI36
NG_028029.1:g.11353T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000525083.6:n.1180T>G
ENST00000532101.6:n.799T>G
ENST00000532125.2:c.694T>G	ENSP00000434178.2:p.Ser232Ala
ENST00000533839.6:c.86-402T>G	ENSP00000509952.1:n.86-402T>G
ENST00000534011.6:n.989T>G
ENST00000685484.1:c.697T>G	ENSP00000510622.1:p.Ser233Ala
ENST00000685601.1:c.697T>G	ENSP00000510603.1:p.Ser233Ala
ENST00000685765.1:c.697T>G	ENSP00000509991.1:p.Ser233Ala
ENST00000685844.1:c.*234T>G	ENSP00000509820.1:n.*234T>G
ENST00000685857.1:n.1436T>G
ENST00000686242.1:c.496T>G	ENSP00000508950.1:n.496T>G
ENST00000686888.1:c.*264T>G	ENSP00000509619.1:n.*264T>G
ENST00000687699.1:c.821T>G	ENSP00000508878.1:n.821T>G
ENST00000687786.1:n.2133T>G
ENST00000688100.1:n.1618T>G
ENST00000688588.1:c.697T>G	ENSP00000510802.1:p.Ser233Ala
ENST00000688927.1:n.2908T>G
ENST00000689283.1:c.*360T>G	ENSP00000509050.1:n.*360T>G
ENST00000689477.1:c.*590T>G	ENSP00000508945.1:n.*590T>G
ENST00000689765.1:c.*190T>G	ENSP00000509625.1:n.*190T>G
ENST00000690512.1:c.*548T>G	ENSP00000509793.1:n.*548T>G
ENST00000692039.1:c.*495T>G	ENSP00000508821.1:n.*495T>G
ENST00000692336.1:c.721T>G	ENSP00000508540.1:p.Ser241Ala
ENST00000693133.1:n.1177T>G
ENST00000263578.10:c.697T>G MANE Select	ENSP00000263578.5:p.Ser233Ala
ENST00000263578.9:c.697T>G	ENSP00000263578.5:p.Ser233Ala
ENST00000525083.5:n.417T>G
ENST00000525770.5:c.*329T>G	ENSP00000434739.1:n.*329T>G
ENST00000527004.5:c.*41T>G	ENSP00000436374.1:n.*41T>G
ENST00000530642.1:n.1479T>G
ENST00000532101.5:n.920T>G
ENST00000532125.1:c.655T>G	ENSP00000434178.1:p.Ser219Ala
ENST00000533395.5:n.430T>G
ENST00000533839.5:n.238-402T>G
ENST00000534011.5:n.749T>G
ENST00000534315.5:n.1009T>G
NM_017547.3:c.697T>G	NP_060017.1:p.Ser233Ala
NR_037647.1:n.643T>G
NR_037648.1:n.883T>G
XM_006718879.2:c.187T>G	XP_006718942.1:p.Ser63Ala
XM_006718880.2:c.64T>G	XP_006718943.1:p.Ser22Ala
XM_006718881.2:c.64T>G	XP_006718944.1:p.Ser22Ala
XM_011542895.1:c.187T>G	XP_011541197.1:p.Ser63Ala
XM_011542896.1:c.187T>G	XP_011541198.1:p.Ser63Ala
XM_006718879.3:c.187T>G	XP_006718942.1:p.Ser63Ala
XM_006718881.3:c.64T>G	XP_006718944.1:p.Ser22Ala
XM_011542895.2:c.187T>G	XP_011541197.1:p.Ser63Ala
XM_011542896.2:c.187T>G	XP_011541198.1:p.Ser63Ala
XM_017018000.2:c.697T>G	XP_016873489.1:p.Ser233Ala
XM_017018001.1:c.187T>G	XP_016873490.1:p.Ser63Ala
XM_017018002.1:c.187T>G	XP_016873491.1:p.Ser63Ala
XM_017018003.2:c.64T>G	XP_016873492.1:p.Ser22Ala
XM_017018004.1:c.64T>G	XP_016873493.1:p.Ser22Ala
XM_017018005.1:c.64T>G	XP_016873494.1:p.Ser22Ala
XM_017018006.2:c.64T>G	XP_016873495.1:p.Ser22Ala
NM_017547.4:c.697T>G MANE Select	NP_060017.1:p.Ser233Ala
NR_037647.2:n.529T>G
NR_037648.2:n.874T>G