Canonical Allele Identifier: CA383230235

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145300T>G (hg19) ; chr11:g.126275405T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275405T>G , CM000673.2:g.126275405T>G	GRCh38
NC_000011.9:g.126145300T>G , CM000673.1:g.126145300T>G	GRCh37
NC_000011.8:g.125650510T>G	NCBI36
NG_028029.1:g.11366T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1193T>G
ENST00000532101.6:n.812T>G
ENST00000532125.2:c.707T>G	ENSP00000434178.2:p.Leu236Arg
ENST00000533839.6:c.86-389T>G	ENSP00000509952.1:n.86-389T>G
ENST00000534011.6:n.1002T>G
ENST00000685484.1:c.710T>G	ENSP00000510622.1:p.Leu237Arg
ENST00000685601.1:c.710T>G	ENSP00000510603.1:p.Leu237Arg
ENST00000685765.1:c.710T>G	ENSP00000509991.1:p.Leu237Arg
ENST00000685844.1:c.*247T>G	ENSP00000509820.1:n.*247T>G
ENST00000685857.1:n.1449T>G
ENST00000686242.1:c.509T>G	ENSP00000508950.1:n.509T>G
ENST00000686888.1:c.*277T>G	ENSP00000509619.1:n.*277T>G
ENST00000687699.1:c.834T>G	ENSP00000508878.1:n.834T>G
ENST00000687786.1:n.2146T>G
ENST00000688100.1:n.1631T>G
ENST00000688588.1:c.710T>G	ENSP00000510802.1:p.Leu237Arg
ENST00000688927.1:n.2921T>G
ENST00000689283.1:c.*373T>G	ENSP00000509050.1:n.*373T>G
ENST00000689477.1:c.*603T>G	ENSP00000508945.1:n.*603T>G
ENST00000689765.1:c.*203T>G	ENSP00000509625.1:n.*203T>G
ENST00000690512.1:c.*561T>G	ENSP00000509793.1:n.*561T>G
ENST00000692039.1:c.*508T>G	ENSP00000508821.1:n.*508T>G
ENST00000692336.1:c.734T>G	ENSP00000508540.1:p.Leu245Arg
ENST00000693133.1:n.1190T>G
ENST00000263578.10:c.710T>G MANE Select	ENSP00000263578.5:p.Leu237Arg
ENST00000263578.9:c.710T>G	ENSP00000263578.5:p.Leu237Arg
ENST00000525083.5:n.430T>G
ENST00000525770.5:c.*342T>G	ENSP00000434739.1:n.*342T>G
ENST00000527004.5:c.*54T>G	ENSP00000436374.1:n.*54T>G
ENST00000530642.1:n.1492T>G
ENST00000532101.5:n.933T>G
ENST00000532125.1:c.668T>G	ENSP00000434178.1:p.Leu223Arg
ENST00000533395.5:n.443T>G
ENST00000533839.5:n.238-389T>G
ENST00000534011.5:n.762T>G
ENST00000534315.5:n.1022T>G
NM_017547.3:c.710T>G	NP_060017.1:p.Leu237Arg
NR_037647.1:n.656T>G
NR_037648.1:n.896T>G
XM_006718879.2:c.200T>G	XP_006718942.1:p.Leu67Arg
XM_006718880.2:c.77T>G	XP_006718943.1:p.Leu26Arg
XM_006718881.2:c.77T>G	XP_006718944.1:p.Leu26Arg
XM_011542895.1:c.200T>G	XP_011541197.1:p.Leu67Arg
XM_011542896.1:c.200T>G	XP_011541198.1:p.Leu67Arg
XM_006718879.3:c.200T>G	XP_006718942.1:p.Leu67Arg
XM_006718881.3:c.77T>G	XP_006718944.1:p.Leu26Arg
XM_011542895.2:c.200T>G	XP_011541197.1:p.Leu67Arg
XM_011542896.2:c.200T>G	XP_011541198.1:p.Leu67Arg
XM_017018000.2:c.710T>G	XP_016873489.1:p.Leu237Arg
XM_017018001.1:c.200T>G	XP_016873490.1:p.Leu67Arg
XM_017018002.1:c.200T>G	XP_016873491.1:p.Leu67Arg
XM_017018003.2:c.77T>G	XP_016873492.1:p.Leu26Arg
XM_017018004.1:c.77T>G	XP_016873493.1:p.Leu26Arg
XM_017018005.1:c.77T>G	XP_016873494.1:p.Leu26Arg
XM_017018006.2:c.77T>G	XP_016873495.1:p.Leu26Arg
NM_017547.4:c.710T>G MANE Select	NP_060017.1:p.Leu237Arg
NR_037647.2:n.542T>G
NR_037648.2:n.887T>G