Canonical Allele Identifier: CA383230029

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126144904T>A (hg19) ; chr11:g.126275009T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275009T>A , CM000673.2:g.126275009T>A	GRCh38
NC_000011.9:g.126144904T>A , CM000673.1:g.126144904T>A	GRCh37
NC_000011.8:g.125650114T>A	NCBI36
NG_028029.1:g.10970T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.797T>A
ENST00000532101.6:n.734-318T>A
ENST00000532125.2:c.616T>A	ENSP00000434178.2:p.Leu206Met
ENST00000533839.6:c.86-785T>A	ENSP00000509952.1:n.86-785T>A
ENST00000534011.6:n.911T>A
ENST00000685484.1:c.619T>A	ENSP00000510622.1:p.Leu207Met
ENST00000685601.1:c.619T>A	ENSP00000510603.1:p.Leu207Met
ENST00000685765.1:c.619T>A	ENSP00000509991.1:p.Leu207Met
ENST00000685844.1:c.*169-318T>A	ENSP00000509820.1:n.*169-318T>A
ENST00000685857.1:n.1053T>A
ENST00000686242.1:c.418T>A	ENSP00000508950.1:n.418T>A
ENST00000686888.1:c.*186T>A	ENSP00000509619.1:n.*186T>A
ENST00000687699.1:c.743T>A	ENSP00000508878.1:n.743T>A
ENST00000687786.1:n.2068-318T>A
ENST00000688100.1:n.1540T>A
ENST00000688588.1:c.619T>A	ENSP00000510802.1:p.Leu207Met
ENST00000688927.1:n.2525T>A
ENST00000689283.1:c.*282T>A	ENSP00000509050.1:n.*282T>A
ENST00000689477.1:c.*512T>A	ENSP00000508945.1:n.*512T>A
ENST00000689765.1:c.*169-362T>A	ENSP00000509625.1:n.*169-362T>A
ENST00000690512.1:c.*470T>A	ENSP00000509793.1:n.*470T>A
ENST00000692039.1:c.*417T>A	ENSP00000508821.1:n.*417T>A
ENST00000692336.1:c.643T>A	ENSP00000508540.1:p.Leu215Met
ENST00000693133.1:n.794T>A
ENST00000263578.10:c.619T>A MANE Select	ENSP00000263578.5:p.Leu207Met
ENST00000263578.9:c.619T>A	ENSP00000263578.5:p.Leu207Met
ENST00000524751.5:n.555T>A
ENST00000525083.5:n.352-318T>A
ENST00000525770.5:c.*251T>A	ENSP00000434739.1:n.*251T>A
ENST00000526366.5:n.550T>A
ENST00000527004.5:c.534-318T>A	ENSP00000436374.1:n.534-318T>A
ENST00000527875.1:n.449T>A
ENST00000530642.1:n.1096T>A
ENST00000532101.5:n.842T>A
ENST00000532125.1:c.577T>A	ENSP00000434178.1:p.Leu193Met
ENST00000533395.5:n.365-318T>A
ENST00000533839.5:n.238-785T>A
ENST00000534011.5:n.671T>A
ENST00000534315.5:n.944-318T>A
NM_017547.3:c.619T>A	NP_060017.1:p.Leu207Met
NR_037647.1:n.565T>A
NR_037648.1:n.805T>A
XM_006718879.2:c.109T>A	XP_006718942.1:p.Leu37Met
XM_006718880.2:c.-2-318T>A	XP_006718943.1:n.-2-318T>A
XM_006718881.2:c.-2-318T>A	XP_006718944.1:n.-2-318T>A
XM_011542895.1:c.109T>A	XP_011541197.1:p.Leu37Met
XM_011542896.1:c.109T>A	XP_011541198.1:p.Leu37Met
XM_006718879.3:c.109T>A	XP_006718942.1:p.Leu37Met
XM_006718881.3:c.-2-318T>A	XP_006718944.1:n.-2-318T>A
XM_011542895.2:c.109T>A	XP_011541197.1:p.Leu37Met
XM_011542896.2:c.109T>A	XP_011541198.1:p.Leu37Met
XM_017018000.2:c.619T>A	XP_016873489.1:p.Leu207Met
XM_017018001.1:c.109T>A	XP_016873490.1:p.Leu37Met
XM_017018002.1:c.109T>A	XP_016873491.1:p.Leu37Met
XM_017018003.2:c.-2-318T>A	XP_016873492.1:n.-2-318T>A
XM_017018004.1:c.-2-318T>A	XP_016873493.1:n.-2-318T>A
XM_017018005.1:c.-2-318T>A	XP_016873494.1:n.-2-318T>A
XM_017018006.2:c.-2-318T>A	XP_016873495.1:n.-2-318T>A
NM_017547.4:c.619T>A MANE Select	NP_060017.1:p.Leu207Met
NR_037647.2:n.451T>A
NR_037648.2:n.796T>A