Canonical Allele Identifier: CA383230259

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145310G>T (hg19) ; chr11:g.126275415G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275415G>T , CM000673.2:g.126275415G>T	GRCh38
NC_000011.9:g.126145310G>T , CM000673.1:g.126145310G>T	GRCh37
NC_000011.8:g.125650520G>T	NCBI36
NG_028029.1:g.11376G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1203G>T
ENST00000532101.6:n.822G>T
ENST00000532125.2:c.717G>T	ENSP00000434178.2:p.Gln239His
ENST00000533839.6:c.86-379G>T	ENSP00000509952.1:n.86-379G>T
ENST00000534011.6:n.1012G>T
ENST00000685484.1:c.720G>T	ENSP00000510622.1:p.Gln240His
ENST00000685601.1:c.720G>T	ENSP00000510603.1:p.Gln240His
ENST00000685765.1:c.720G>T	ENSP00000509991.1:p.Gln240His
ENST00000685844.1:c.*257G>T	ENSP00000509820.1:n.*257G>T
ENST00000685857.1:n.1459G>T
ENST00000686242.1:c.519G>T	ENSP00000508950.1:n.519G>T
ENST00000686888.1:c.*287G>T	ENSP00000509619.1:n.*287G>T
ENST00000687699.1:c.844G>T	ENSP00000508878.1:n.844G>T
ENST00000687786.1:n.2156G>T
ENST00000688100.1:n.1641G>T
ENST00000688588.1:c.720G>T	ENSP00000510802.1:p.Gln240His
ENST00000688927.1:n.2931G>T
ENST00000689283.1:c.*383G>T	ENSP00000509050.1:n.*383G>T
ENST00000689477.1:c.*613G>T	ENSP00000508945.1:n.*613G>T
ENST00000689765.1:c.*213G>T	ENSP00000509625.1:n.*213G>T
ENST00000690512.1:c.*571G>T	ENSP00000509793.1:n.*571G>T
ENST00000692039.1:c.*518G>T	ENSP00000508821.1:n.*518G>T
ENST00000692336.1:c.744G>T	ENSP00000508540.1:p.Gln248His
ENST00000693133.1:n.1200G>T
ENST00000263578.10:c.720G>T MANE Select	ENSP00000263578.5:p.Gln240His
ENST00000263578.9:c.720G>T	ENSP00000263578.5:p.Gln240His
ENST00000525083.5:n.440G>T
ENST00000525770.5:c.*352G>T	ENSP00000434739.1:n.*352G>T
ENST00000527004.5:c.*64G>T	ENSP00000436374.1:n.*64G>T
ENST00000530642.1:n.1502G>T
ENST00000532101.5:n.943G>T
ENST00000532125.1:c.678G>T	ENSP00000434178.1:p.Gln226His
ENST00000533395.5:n.453G>T
ENST00000533839.5:n.238-379G>T
ENST00000534011.5:n.772G>T
ENST00000534315.5:n.1032G>T
NM_017547.3:c.720G>T	NP_060017.1:p.Gln240His
NR_037647.1:n.666G>T
NR_037648.1:n.906G>T
XM_006718879.2:c.210G>T	XP_006718942.1:p.Gln70His
XM_006718880.2:c.87G>T	XP_006718943.1:p.Gln29His
XM_006718881.2:c.87G>T	XP_006718944.1:p.Gln29His
XM_011542895.1:c.210G>T	XP_011541197.1:p.Gln70His
XM_011542896.1:c.210G>T	XP_011541198.1:p.Gln70His
XM_006718879.3:c.210G>T	XP_006718942.1:p.Gln70His
XM_006718881.3:c.87G>T	XP_006718944.1:p.Gln29His
XM_011542895.2:c.210G>T	XP_011541197.1:p.Gln70His
XM_011542896.2:c.210G>T	XP_011541198.1:p.Gln70His
XM_017018000.2:c.720G>T	XP_016873489.1:p.Gln240His
XM_017018001.1:c.210G>T	XP_016873490.1:p.Gln70His
XM_017018002.1:c.210G>T	XP_016873491.1:p.Gln70His
XM_017018003.2:c.87G>T	XP_016873492.1:p.Gln29His
XM_017018004.1:c.87G>T	XP_016873493.1:p.Gln29His
XM_017018005.1:c.87G>T	XP_016873494.1:p.Gln29His
XM_017018006.2:c.87G>T	XP_016873495.1:p.Gln29His
NM_017547.4:c.720G>T MANE Select	NP_060017.1:p.Gln240His
NR_037647.2:n.552G>T
NR_037648.2:n.897G>T