Canonical Allele Identifier: CA383230244

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145305T>A (hg19) ; chr11:g.126275410T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275410T>A , CM000673.2:g.126275410T>A	GRCh38
NC_000011.9:g.126145305T>A , CM000673.1:g.126145305T>A	GRCh37
NC_000011.8:g.125650515T>A	NCBI36
NG_028029.1:g.11371T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1198T>A
ENST00000532101.6:n.817T>A
ENST00000532125.2:c.712T>A	ENSP00000434178.2:p.Cys238Ser
ENST00000533839.6:c.86-384T>A	ENSP00000509952.1:n.86-384T>A
ENST00000534011.6:n.1007T>A
ENST00000685484.1:c.715T>A	ENSP00000510622.1:p.Cys239Ser
ENST00000685601.1:c.715T>A	ENSP00000510603.1:p.Cys239Ser
ENST00000685765.1:c.715T>A	ENSP00000509991.1:p.Cys239Ser
ENST00000685844.1:c.*252T>A	ENSP00000509820.1:n.*252T>A
ENST00000685857.1:n.1454T>A
ENST00000686242.1:c.514T>A	ENSP00000508950.1:n.514T>A
ENST00000686888.1:c.*282T>A	ENSP00000509619.1:n.*282T>A
ENST00000687699.1:c.839T>A	ENSP00000508878.1:n.839T>A
ENST00000687786.1:n.2151T>A
ENST00000688100.1:n.1636T>A
ENST00000688588.1:c.715T>A	ENSP00000510802.1:p.Cys239Ser
ENST00000688927.1:n.2926T>A
ENST00000689283.1:c.*378T>A	ENSP00000509050.1:n.*378T>A
ENST00000689477.1:c.*608T>A	ENSP00000508945.1:n.*608T>A
ENST00000689765.1:c.*208T>A	ENSP00000509625.1:n.*208T>A
ENST00000690512.1:c.*566T>A	ENSP00000509793.1:n.*566T>A
ENST00000692039.1:c.*513T>A	ENSP00000508821.1:n.*513T>A
ENST00000692336.1:c.739T>A	ENSP00000508540.1:p.Cys247Ser
ENST00000693133.1:n.1195T>A
ENST00000263578.10:c.715T>A MANE Select	ENSP00000263578.5:p.Cys239Ser
ENST00000263578.9:c.715T>A	ENSP00000263578.5:p.Cys239Ser
ENST00000525083.5:n.435T>A
ENST00000525770.5:c.*347T>A	ENSP00000434739.1:n.*347T>A
ENST00000527004.5:c.*59T>A	ENSP00000436374.1:n.*59T>A
ENST00000530642.1:n.1497T>A
ENST00000532101.5:n.938T>A
ENST00000532125.1:c.673T>A	ENSP00000434178.1:p.Cys225Ser
ENST00000533395.5:n.448T>A
ENST00000533839.5:n.238-384T>A
ENST00000534011.5:n.767T>A
ENST00000534315.5:n.1027T>A
NM_017547.3:c.715T>A	NP_060017.1:p.Cys239Ser
NR_037647.1:n.661T>A
NR_037648.1:n.901T>A
XM_006718879.2:c.205T>A	XP_006718942.1:p.Cys69Ser
XM_006718880.2:c.82T>A	XP_006718943.1:p.Cys28Ser
XM_006718881.2:c.82T>A	XP_006718944.1:p.Cys28Ser
XM_011542895.1:c.205T>A	XP_011541197.1:p.Cys69Ser
XM_011542896.1:c.205T>A	XP_011541198.1:p.Cys69Ser
XM_006718879.3:c.205T>A	XP_006718942.1:p.Cys69Ser
XM_006718881.3:c.82T>A	XP_006718944.1:p.Cys28Ser
XM_011542895.2:c.205T>A	XP_011541197.1:p.Cys69Ser
XM_011542896.2:c.205T>A	XP_011541198.1:p.Cys69Ser
XM_017018000.2:c.715T>A	XP_016873489.1:p.Cys239Ser
XM_017018001.1:c.205T>A	XP_016873490.1:p.Cys69Ser
XM_017018002.1:c.205T>A	XP_016873491.1:p.Cys69Ser
XM_017018003.2:c.82T>A	XP_016873492.1:p.Cys28Ser
XM_017018004.1:c.82T>A	XP_016873493.1:p.Cys28Ser
XM_017018005.1:c.82T>A	XP_016873494.1:p.Cys28Ser
XM_017018006.2:c.82T>A	XP_016873495.1:p.Cys28Ser
NM_017547.4:c.715T>A MANE Select	NP_060017.1:p.Cys239Ser
NR_037647.2:n.547T>A
NR_037648.2:n.892T>A