Canonical Allele Identifier: CA383230193

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145279A>T (hg19) ; chr11:g.126275384A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275384A>T , CM000673.2:g.126275384A>T	GRCh38
NC_000011.9:g.126145279A>T , CM000673.1:g.126145279A>T	GRCh37
NC_000011.8:g.125650489A>T	NCBI36
NG_028029.1:g.11345A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1172A>T
ENST00000532101.6:n.791A>T
ENST00000532125.2:c.686A>T	ENSP00000434178.2:p.Lys229Met
ENST00000533839.6:c.86-410A>T	ENSP00000509952.1:n.86-410A>T
ENST00000534011.6:n.981A>T
ENST00000685484.1:c.689A>T	ENSP00000510622.1:p.Lys230Met
ENST00000685601.1:c.689A>T	ENSP00000510603.1:p.Lys230Met
ENST00000685765.1:c.689A>T	ENSP00000509991.1:p.Lys230Met
ENST00000685844.1:c.*226A>T	ENSP00000509820.1:n.*226A>T
ENST00000685857.1:n.1428A>T
ENST00000686242.1:c.488A>T	ENSP00000508950.1:n.488A>T
ENST00000686888.1:c.*256A>T	ENSP00000509619.1:n.*256A>T
ENST00000687699.1:c.813A>T	ENSP00000508878.1:n.813A>T
ENST00000687786.1:n.2125A>T
ENST00000688100.1:n.1610A>T
ENST00000688588.1:c.689A>T	ENSP00000510802.1:p.Lys230Met
ENST00000688927.1:n.2900A>T
ENST00000689283.1:c.*352A>T	ENSP00000509050.1:n.*352A>T
ENST00000689477.1:c.*582A>T	ENSP00000508945.1:n.*582A>T
ENST00000689765.1:c.*182A>T	ENSP00000509625.1:n.*182A>T
ENST00000690512.1:c.*540A>T	ENSP00000509793.1:n.*540A>T
ENST00000692039.1:c.*487A>T	ENSP00000508821.1:n.*487A>T
ENST00000692336.1:c.713A>T	ENSP00000508540.1:p.Lys238Met
ENST00000693133.1:n.1169A>T
ENST00000263578.10:c.689A>T MANE Select	ENSP00000263578.5:p.Lys230Met
ENST00000263578.9:c.689A>T	ENSP00000263578.5:p.Lys230Met
ENST00000525083.5:n.409A>T
ENST00000525770.5:c.*321A>T	ENSP00000434739.1:n.*321A>T
ENST00000527004.5:c.*33A>T	ENSP00000436374.1:n.*33A>T
ENST00000530642.1:n.1471A>T
ENST00000532101.5:n.912A>T
ENST00000532125.1:c.647A>T	ENSP00000434178.1:p.Lys216Met
ENST00000533395.5:n.422A>T
ENST00000533839.5:n.238-410A>T
ENST00000534011.5:n.741A>T
ENST00000534315.5:n.1001A>T
NM_017547.3:c.689A>T	NP_060017.1:p.Lys230Met
NR_037647.1:n.635A>T
NR_037648.1:n.875A>T
XM_006718879.2:c.179A>T	XP_006718942.1:p.Lys60Met
XM_006718880.2:c.56A>T	XP_006718943.1:p.Lys19Met
XM_006718881.2:c.56A>T	XP_006718944.1:p.Lys19Met
XM_011542895.1:c.179A>T	XP_011541197.1:p.Lys60Met
XM_011542896.1:c.179A>T	XP_011541198.1:p.Lys60Met
XM_006718879.3:c.179A>T	XP_006718942.1:p.Lys60Met
XM_006718881.3:c.56A>T	XP_006718944.1:p.Lys19Met
XM_011542895.2:c.179A>T	XP_011541197.1:p.Lys60Met
XM_011542896.2:c.179A>T	XP_011541198.1:p.Lys60Met
XM_017018000.2:c.689A>T	XP_016873489.1:p.Lys230Met
XM_017018001.1:c.179A>T	XP_016873490.1:p.Lys60Met
XM_017018002.1:c.179A>T	XP_016873491.1:p.Lys60Met
XM_017018003.2:c.56A>T	XP_016873492.1:p.Lys19Met
XM_017018004.1:c.56A>T	XP_016873493.1:p.Lys19Met
XM_017018005.1:c.56A>T	XP_016873494.1:p.Lys19Met
XM_017018006.2:c.56A>T	XP_016873495.1:p.Lys19Met
NM_017547.4:c.689A>T MANE Select	NP_060017.1:p.Lys230Met
NR_037647.2:n.521A>T
NR_037648.2:n.866A>T