Canonical Allele Identifier: CA383230122

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145243T>G (hg19) ; chr11:g.126275348T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275348T>G , CM000673.2:g.126275348T>G	GRCh38
NC_000011.9:g.126145243T>G , CM000673.1:g.126145243T>G	GRCh37
NC_000011.8:g.125650453T>G	NCBI36
NG_028029.1:g.11309T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1136T>G
ENST00000532101.6:n.755T>G
ENST00000532125.2:c.650T>G	ENSP00000434178.2:p.Phe217Cys
ENST00000533839.6:c.86-446T>G	ENSP00000509952.1:n.86-446T>G
ENST00000534011.6:n.945T>G
ENST00000685484.1:c.653T>G	ENSP00000510622.1:p.Phe218Cys
ENST00000685601.1:c.653T>G	ENSP00000510603.1:p.Phe218Cys
ENST00000685765.1:c.653T>G	ENSP00000509991.1:p.Phe218Cys
ENST00000685844.1:c.*190T>G	ENSP00000509820.1:n.*190T>G
ENST00000685857.1:n.1392T>G
ENST00000686242.1:c.452T>G	ENSP00000508950.1:n.452T>G
ENST00000686888.1:c.*220T>G	ENSP00000509619.1:n.*220T>G
ENST00000687699.1:c.777T>G	ENSP00000508878.1:n.777T>G
ENST00000687786.1:n.2089T>G
ENST00000688100.1:n.1574T>G
ENST00000688588.1:c.653T>G	ENSP00000510802.1:p.Phe218Cys
ENST00000688927.1:n.2864T>G
ENST00000689283.1:c.*316T>G	ENSP00000509050.1:n.*316T>G
ENST00000689477.1:c.*546T>G	ENSP00000508945.1:n.*546T>G
ENST00000689765.1:c.*169-23T>G	ENSP00000509625.1:n.*169-23T>G
ENST00000690512.1:c.*504T>G	ENSP00000509793.1:n.*504T>G
ENST00000692039.1:c.*451T>G	ENSP00000508821.1:n.*451T>G
ENST00000692336.1:c.677T>G	ENSP00000508540.1:p.Phe226Cys
ENST00000693133.1:n.1133T>G
ENST00000263578.10:c.653T>G MANE Select	ENSP00000263578.5:p.Phe218Cys
ENST00000263578.9:c.653T>G	ENSP00000263578.5:p.Phe218Cys
ENST00000524751.5:n.894T>G
ENST00000525083.5:n.373T>G
ENST00000525770.5:c.*285T>G	ENSP00000434739.1:n.*285T>G
ENST00000527004.5:c.555T>G	ENSP00000436374.1:p.Val185=
ENST00000530642.1:n.1435T>G
ENST00000532101.5:n.876T>G
ENST00000532125.1:c.611T>G	ENSP00000434178.1:p.Phe204Cys
ENST00000533395.5:n.386T>G
ENST00000533839.5:n.238-446T>G
ENST00000534011.5:n.705T>G
ENST00000534315.5:n.965T>G
NM_017547.3:c.653T>G	NP_060017.1:p.Phe218Cys
NR_037647.1:n.599T>G
NR_037648.1:n.839T>G
XM_006718879.2:c.143T>G	XP_006718942.1:p.Phe48Cys
XM_006718880.2:c.20T>G	XP_006718943.1:p.Phe7Cys
XM_006718881.2:c.20T>G	XP_006718944.1:p.Phe7Cys
XM_011542895.1:c.143T>G	XP_011541197.1:p.Phe48Cys
XM_011542896.1:c.143T>G	XP_011541198.1:p.Phe48Cys
XM_006718879.3:c.143T>G	XP_006718942.1:p.Phe48Cys
XM_006718881.3:c.20T>G	XP_006718944.1:p.Phe7Cys
XM_011542895.2:c.143T>G	XP_011541197.1:p.Phe48Cys
XM_011542896.2:c.143T>G	XP_011541198.1:p.Phe48Cys
XM_017018000.2:c.653T>G	XP_016873489.1:p.Phe218Cys
XM_017018001.1:c.143T>G	XP_016873490.1:p.Phe48Cys
XM_017018002.1:c.143T>G	XP_016873491.1:p.Phe48Cys
XM_017018003.2:c.20T>G	XP_016873492.1:p.Phe7Cys
XM_017018004.1:c.20T>G	XP_016873493.1:p.Phe7Cys
XM_017018005.1:c.20T>G	XP_016873494.1:p.Phe7Cys
XM_017018006.2:c.20T>G	XP_016873495.1:p.Phe7Cys
NM_017547.4:c.653T>G MANE Select	NP_060017.1:p.Phe218Cys
NR_037647.2:n.485T>G
NR_037648.2:n.830T>G