Canonical Allele Identifier: CA383230035

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126144906G>T (hg19) ; chr11:g.126275011G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275011G>T , CM000673.2:g.126275011G>T	GRCh38
NC_000011.9:g.126144906G>T , CM000673.1:g.126144906G>T	GRCh37
NC_000011.8:g.125650116G>T	NCBI36
NG_028029.1:g.10972G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.799G>T
ENST00000532101.6:n.734-316G>T
ENST00000532125.2:c.618G>T	ENSP00000434178.2:p.Leu206Phe
ENST00000533839.6:c.86-783G>T	ENSP00000509952.1:n.86-783G>T
ENST00000534011.6:n.913G>T
ENST00000685484.1:c.621G>T	ENSP00000510622.1:p.Leu207Phe
ENST00000685601.1:c.621G>T	ENSP00000510603.1:p.Leu207Phe
ENST00000685765.1:c.621G>T	ENSP00000509991.1:p.Leu207Phe
ENST00000685844.1:c.*169-316G>T	ENSP00000509820.1:n.*169-316G>T
ENST00000685857.1:n.1055G>T
ENST00000686242.1:c.420G>T	ENSP00000508950.1:n.420G>T
ENST00000686888.1:c.*188G>T	ENSP00000509619.1:n.*188G>T
ENST00000687699.1:c.745G>T	ENSP00000508878.1:n.745G>T
ENST00000687786.1:n.2068-316G>T
ENST00000688100.1:n.1542G>T
ENST00000688588.1:c.621G>T	ENSP00000510802.1:p.Leu207Phe
ENST00000688927.1:n.2527G>T
ENST00000689283.1:c.*284G>T	ENSP00000509050.1:n.*284G>T
ENST00000689477.1:c.*514G>T	ENSP00000508945.1:n.*514G>T
ENST00000689765.1:c.*169-360G>T	ENSP00000509625.1:n.*169-360G>T
ENST00000690512.1:c.*472G>T	ENSP00000509793.1:n.*472G>T
ENST00000692039.1:c.*419G>T	ENSP00000508821.1:n.*419G>T
ENST00000692336.1:c.645G>T	ENSP00000508540.1:p.Leu215Phe
ENST00000693133.1:n.796G>T
ENST00000263578.10:c.621G>T MANE Select	ENSP00000263578.5:p.Leu207Phe
ENST00000263578.9:c.621G>T	ENSP00000263578.5:p.Leu207Phe
ENST00000524751.5:n.557G>T
ENST00000525083.5:n.352-316G>T
ENST00000525770.5:c.*253G>T	ENSP00000434739.1:n.*253G>T
ENST00000526366.5:n.552G>T
ENST00000527004.5:c.534-316G>T	ENSP00000436374.1:n.534-316G>T
ENST00000527875.1:n.451G>T
ENST00000530642.1:n.1098G>T
ENST00000532101.5:n.844G>T
ENST00000532125.1:c.579G>T	ENSP00000434178.1:p.Leu193Phe
ENST00000533395.5:n.365-316G>T
ENST00000533839.5:n.238-783G>T
ENST00000534011.5:n.673G>T
ENST00000534315.5:n.944-316G>T
NM_017547.3:c.621G>T	NP_060017.1:p.Leu207Phe
NR_037647.1:n.567G>T
NR_037648.1:n.807G>T
XM_006718879.2:c.111G>T	XP_006718942.1:p.Leu37Phe
XM_006718880.2:c.-2-316G>T	XP_006718943.1:n.-2-316G>T
XM_006718881.2:c.-2-316G>T	XP_006718944.1:n.-2-316G>T
XM_011542895.1:c.111G>T	XP_011541197.1:p.Leu37Phe
XM_011542896.1:c.111G>T	XP_011541198.1:p.Leu37Phe
XM_006718879.3:c.111G>T	XP_006718942.1:p.Leu37Phe
XM_006718881.3:c.-2-316G>T	XP_006718944.1:n.-2-316G>T
XM_011542895.2:c.111G>T	XP_011541197.1:p.Leu37Phe
XM_011542896.2:c.111G>T	XP_011541198.1:p.Leu37Phe
XM_017018000.2:c.621G>T	XP_016873489.1:p.Leu207Phe
XM_017018001.1:c.111G>T	XP_016873490.1:p.Leu37Phe
XM_017018002.1:c.111G>T	XP_016873491.1:p.Leu37Phe
XM_017018003.2:c.-2-316G>T	XP_016873492.1:n.-2-316G>T
XM_017018004.1:c.-2-316G>T	XP_016873493.1:n.-2-316G>T
XM_017018005.1:c.-2-316G>T	XP_016873494.1:n.-2-316G>T
XM_017018006.2:c.-2-316G>T	XP_016873495.1:n.-2-316G>T
NM_017547.4:c.621G>T MANE Select	NP_060017.1:p.Leu207Phe
NR_037647.2:n.453G>T
NR_037648.2:n.798G>T