Canonical Allele Identifier: CA383230162

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145261T>G (hg19) ; chr11:g.126275366T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275366T>G , CM000673.2:g.126275366T>G	GRCh38
NC_000011.9:g.126145261T>G , CM000673.1:g.126145261T>G	GRCh37
NC_000011.8:g.125650471T>G	NCBI36
NG_028029.1:g.11327T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1154T>G
ENST00000532101.6:n.773T>G
ENST00000532125.2:c.668T>G	ENSP00000434178.2:p.Leu223Arg
ENST00000533839.6:c.86-428T>G	ENSP00000509952.1:n.86-428T>G
ENST00000534011.6:n.963T>G
ENST00000685484.1:c.671T>G	ENSP00000510622.1:p.Leu224Arg
ENST00000685601.1:c.671T>G	ENSP00000510603.1:p.Leu224Arg
ENST00000685765.1:c.671T>G	ENSP00000509991.1:p.Leu224Arg
ENST00000685844.1:c.*208T>G	ENSP00000509820.1:n.*208T>G
ENST00000685857.1:n.1410T>G
ENST00000686242.1:c.470T>G	ENSP00000508950.1:n.470T>G
ENST00000686888.1:c.*238T>G	ENSP00000509619.1:n.*238T>G
ENST00000687699.1:c.795T>G	ENSP00000508878.1:n.795T>G
ENST00000687786.1:n.2107T>G
ENST00000688100.1:n.1592T>G
ENST00000688588.1:c.671T>G	ENSP00000510802.1:p.Leu224Arg
ENST00000688927.1:n.2882T>G
ENST00000689283.1:c.*334T>G	ENSP00000509050.1:n.*334T>G
ENST00000689477.1:c.*564T>G	ENSP00000508945.1:n.*564T>G
ENST00000689765.1:c.*169-5T>G	ENSP00000509625.1:n.*169-5T>G
ENST00000690512.1:c.*522T>G	ENSP00000509793.1:n.*522T>G
ENST00000692039.1:c.*469T>G	ENSP00000508821.1:n.*469T>G
ENST00000692336.1:c.695T>G	ENSP00000508540.1:p.Leu232Arg
ENST00000693133.1:n.1151T>G
ENST00000263578.10:c.671T>G MANE Select	ENSP00000263578.5:p.Leu224Arg
ENST00000263578.9:c.671T>G	ENSP00000263578.5:p.Leu224Arg
ENST00000525083.5:n.391T>G
ENST00000525770.5:c.*303T>G	ENSP00000434739.1:n.*303T>G
ENST00000527004.5:c.*15T>G	ENSP00000436374.1:n.*15T>G
ENST00000530642.1:n.1453T>G
ENST00000532101.5:n.894T>G
ENST00000532125.1:c.629T>G	ENSP00000434178.1:p.Leu210Arg
ENST00000533395.5:n.404T>G
ENST00000533839.5:n.238-428T>G
ENST00000534011.5:n.723T>G
ENST00000534315.5:n.983T>G
NM_017547.3:c.671T>G	NP_060017.1:p.Leu224Arg
NR_037647.1:n.617T>G
NR_037648.1:n.857T>G
XM_006718879.2:c.161T>G	XP_006718942.1:p.Leu54Arg
XM_006718880.2:c.38T>G	XP_006718943.1:p.Leu13Arg
XM_006718881.2:c.38T>G	XP_006718944.1:p.Leu13Arg
XM_011542895.1:c.161T>G	XP_011541197.1:p.Leu54Arg
XM_011542896.1:c.161T>G	XP_011541198.1:p.Leu54Arg
XM_006718879.3:c.161T>G	XP_006718942.1:p.Leu54Arg
XM_006718881.3:c.38T>G	XP_006718944.1:p.Leu13Arg
XM_011542895.2:c.161T>G	XP_011541197.1:p.Leu54Arg
XM_011542896.2:c.161T>G	XP_011541198.1:p.Leu54Arg
XM_017018000.2:c.671T>G	XP_016873489.1:p.Leu224Arg
XM_017018001.1:c.161T>G	XP_016873490.1:p.Leu54Arg
XM_017018002.1:c.161T>G	XP_016873491.1:p.Leu54Arg
XM_017018003.2:c.38T>G	XP_016873492.1:p.Leu13Arg
XM_017018004.1:c.38T>G	XP_016873493.1:p.Leu13Arg
XM_017018005.1:c.38T>G	XP_016873494.1:p.Leu13Arg
XM_017018006.2:c.38T>G	XP_016873495.1:p.Leu13Arg
NM_017547.4:c.671T>G MANE Select	NP_060017.1:p.Leu224Arg
NR_037647.2:n.503T>G
NR_037648.2:n.848T>G