Canonical Allele Identifier: CA383230095

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145232C>G (hg19) ; chr11:g.126275337C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275337C>G , CM000673.2:g.126275337C>G	GRCh38
NC_000011.9:g.126145232C>G , CM000673.1:g.126145232C>G	GRCh37
NC_000011.8:g.125650442C>G	NCBI36
NG_028029.1:g.11298C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1125C>G
ENST00000532101.6:n.744C>G
ENST00000532125.2:c.639C>G	ENSP00000434178.2:p.Asp213Glu
ENST00000533839.6:c.86-457C>G	ENSP00000509952.1:n.86-457C>G
ENST00000534011.6:n.934C>G
ENST00000685484.1:c.642C>G	ENSP00000510622.1:p.Asp214Glu
ENST00000685601.1:c.642C>G	ENSP00000510603.1:p.Asp214Glu
ENST00000685765.1:c.642C>G	ENSP00000509991.1:p.Asp214Glu
ENST00000685844.1:c.*179C>G	ENSP00000509820.1:n.*179C>G
ENST00000685857.1:n.1381C>G
ENST00000686242.1:c.441C>G	ENSP00000508950.1:n.441C>G
ENST00000686888.1:c.*209C>G	ENSP00000509619.1:n.*209C>G
ENST00000687699.1:c.766C>G	ENSP00000508878.1:n.766C>G
ENST00000687786.1:n.2078C>G
ENST00000688100.1:n.1563C>G
ENST00000688588.1:c.642C>G	ENSP00000510802.1:p.Asp214Glu
ENST00000688927.1:n.2853C>G
ENST00000689283.1:c.*305C>G	ENSP00000509050.1:n.*305C>G
ENST00000689477.1:c.*535C>G	ENSP00000508945.1:n.*535C>G
ENST00000689765.1:c.*169-34C>G	ENSP00000509625.1:n.*169-34C>G
ENST00000690512.1:c.*493C>G	ENSP00000509793.1:n.*493C>G
ENST00000692039.1:c.*440C>G	ENSP00000508821.1:n.*440C>G
ENST00000692336.1:c.666C>G	ENSP00000508540.1:p.Asp222Glu
ENST00000693133.1:n.1122C>G
ENST00000263578.10:c.642C>G MANE Select	ENSP00000263578.5:p.Asp214Glu
ENST00000263578.9:c.642C>G	ENSP00000263578.5:p.Asp214Glu
ENST00000524751.5:n.883C>G
ENST00000525083.5:n.362C>G
ENST00000525770.5:c.*274C>G	ENSP00000434739.1:n.*274C>G
ENST00000527004.5:c.544C>G	ENSP00000436374.1:p.Arg182Gly
ENST00000530642.1:n.1424C>G
ENST00000532101.5:n.865C>G
ENST00000532125.1:c.600C>G	ENSP00000434178.1:p.Asp200Glu
ENST00000533395.5:n.375C>G
ENST00000533839.5:n.238-457C>G
ENST00000534011.5:n.694C>G
ENST00000534315.5:n.954C>G
NM_017547.3:c.642C>G	NP_060017.1:p.Asp214Glu
NR_037647.1:n.588C>G
NR_037648.1:n.828C>G
XM_006718879.2:c.132C>G	XP_006718942.1:p.Asp44Glu
XM_006718880.2:c.9C>G	XP_006718943.1:p.Asp3Glu
XM_006718881.2:c.9C>G	XP_006718944.1:p.Asp3Glu
XM_011542895.1:c.132C>G	XP_011541197.1:p.Asp44Glu
XM_011542896.1:c.132C>G	XP_011541198.1:p.Asp44Glu
XM_006718879.3:c.132C>G	XP_006718942.1:p.Asp44Glu
XM_006718881.3:c.9C>G	XP_006718944.1:p.Asp3Glu
XM_011542895.2:c.132C>G	XP_011541197.1:p.Asp44Glu
XM_011542896.2:c.132C>G	XP_011541198.1:p.Asp44Glu
XM_017018000.2:c.642C>G	XP_016873489.1:p.Asp214Glu
XM_017018001.1:c.132C>G	XP_016873490.1:p.Asp44Glu
XM_017018002.1:c.132C>G	XP_016873491.1:p.Asp44Glu
XM_017018003.2:c.9C>G	XP_016873492.1:p.Asp3Glu
XM_017018004.1:c.9C>G	XP_016873493.1:p.Asp3Glu
XM_017018005.1:c.9C>G	XP_016873494.1:p.Asp3Glu
XM_017018006.2:c.9C>G	XP_016873495.1:p.Asp3Glu
NM_017547.4:c.642C>G MANE Select	NP_060017.1:p.Asp214Glu
NR_037647.2:n.474C>G
NR_037648.2:n.819C>G