Canonical Allele Identifier: CA383230211

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145288C>G (hg19) ; chr11:g.126275393C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275393C>G , CM000673.2:g.126275393C>G	GRCh38
NC_000011.9:g.126145288C>G , CM000673.1:g.126145288C>G	GRCh37
NC_000011.8:g.125650498C>G	NCBI36
NG_028029.1:g.11354C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000525083.6:n.1181C>G
ENST00000532101.6:n.800C>G
ENST00000532125.2:c.695C>G	ENSP00000434178.2:p.Ser232Cys
ENST00000533839.6:c.86-401C>G	ENSP00000509952.1:n.86-401C>G
ENST00000534011.6:n.990C>G
ENST00000685484.1:c.698C>G	ENSP00000510622.1:p.Ser233Cys
ENST00000685601.1:c.698C>G	ENSP00000510603.1:p.Ser233Cys
ENST00000685765.1:c.698C>G	ENSP00000509991.1:p.Ser233Cys
ENST00000685844.1:c.*235C>G	ENSP00000509820.1:n.*235C>G
ENST00000685857.1:n.1437C>G
ENST00000686242.1:c.497C>G	ENSP00000508950.1:n.497C>G
ENST00000686888.1:c.*265C>G	ENSP00000509619.1:n.*265C>G
ENST00000687699.1:c.822C>G	ENSP00000508878.1:n.822C>G
ENST00000687786.1:n.2134C>G
ENST00000688100.1:n.1619C>G
ENST00000688588.1:c.698C>G	ENSP00000510802.1:p.Ser233Cys
ENST00000688927.1:n.2909C>G
ENST00000689283.1:c.*361C>G	ENSP00000509050.1:n.*361C>G
ENST00000689477.1:c.*591C>G	ENSP00000508945.1:n.*591C>G
ENST00000689765.1:c.*191C>G	ENSP00000509625.1:n.*191C>G
ENST00000690512.1:c.*549C>G	ENSP00000509793.1:n.*549C>G
ENST00000692039.1:c.*496C>G	ENSP00000508821.1:n.*496C>G
ENST00000692336.1:c.722C>G	ENSP00000508540.1:p.Ser241Cys
ENST00000693133.1:n.1178C>G
ENST00000263578.10:c.698C>G MANE Select	ENSP00000263578.5:p.Ser233Cys
ENST00000263578.9:c.698C>G	ENSP00000263578.5:p.Ser233Cys
ENST00000525083.5:n.418C>G
ENST00000525770.5:c.*330C>G	ENSP00000434739.1:n.*330C>G
ENST00000527004.5:c.*42C>G	ENSP00000436374.1:n.*42C>G
ENST00000530642.1:n.1480C>G
ENST00000532101.5:n.921C>G
ENST00000532125.1:c.656C>G	ENSP00000434178.1:p.Ser219Cys
ENST00000533395.5:n.431C>G
ENST00000533839.5:n.238-401C>G
ENST00000534011.5:n.750C>G
ENST00000534315.5:n.1010C>G
NM_017547.3:c.698C>G	NP_060017.1:p.Ser233Cys
NR_037647.1:n.644C>G
NR_037648.1:n.884C>G
XM_006718879.2:c.188C>G	XP_006718942.1:p.Ser63Cys
XM_006718880.2:c.65C>G	XP_006718943.1:p.Ser22Cys
XM_006718881.2:c.65C>G	XP_006718944.1:p.Ser22Cys
XM_011542895.1:c.188C>G	XP_011541197.1:p.Ser63Cys
XM_011542896.1:c.188C>G	XP_011541198.1:p.Ser63Cys
XM_006718879.3:c.188C>G	XP_006718942.1:p.Ser63Cys
XM_006718881.3:c.65C>G	XP_006718944.1:p.Ser22Cys
XM_011542895.2:c.188C>G	XP_011541197.1:p.Ser63Cys
XM_011542896.2:c.188C>G	XP_011541198.1:p.Ser63Cys
XM_017018000.2:c.698C>G	XP_016873489.1:p.Ser233Cys
XM_017018001.1:c.188C>G	XP_016873490.1:p.Ser63Cys
XM_017018002.1:c.188C>G	XP_016873491.1:p.Ser63Cys
XM_017018003.2:c.65C>G	XP_016873492.1:p.Ser22Cys
XM_017018004.1:c.65C>G	XP_016873493.1:p.Ser22Cys
XM_017018005.1:c.65C>G	XP_016873494.1:p.Ser22Cys
XM_017018006.2:c.65C>G	XP_016873495.1:p.Ser22Cys
NM_017547.4:c.698C>G MANE Select	NP_060017.1:p.Ser233Cys
NR_037647.2:n.530C>G
NR_037648.2:n.875C>G