Canonical Allele Identifier: CA383230107

Gene: FOXRED1

Linked Data

• dbSNP Id: rs770234474
• MyVariant Identifiers: chr11:g.126145237G>T (hg19) ; chr11:g.126275342G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275342G>T , CM000673.2:g.126275342G>T	GRCh38
NC_000011.9:g.126145237G>T , CM000673.1:g.126145237G>T	GRCh37
NC_000011.8:g.125650447G>T	NCBI36
NG_028029.1:g.11303G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1130G>T
ENST00000532101.6:n.749G>T
ENST00000532125.2:c.644G>T	ENSP00000434178.2:p.Gly215Val
ENST00000533839.6:c.86-452G>T	ENSP00000509952.1:n.86-452G>T
ENST00000534011.6:n.939G>T
ENST00000685484.1:c.647G>T	ENSP00000510622.1:p.Gly216Val
ENST00000685601.1:c.647G>T	ENSP00000510603.1:p.Gly216Val
ENST00000685765.1:c.647G>T	ENSP00000509991.1:p.Gly216Val
ENST00000685844.1:c.*184G>T	ENSP00000509820.1:n.*184G>T
ENST00000685857.1:n.1386G>T
ENST00000686242.1:c.446G>T	ENSP00000508950.1:n.446G>T
ENST00000686888.1:c.*214G>T	ENSP00000509619.1:n.*214G>T
ENST00000687699.1:c.771G>T	ENSP00000508878.1:n.771G>T
ENST00000687786.1:n.2083G>T
ENST00000688100.1:n.1568G>T
ENST00000688588.1:c.647G>T	ENSP00000510802.1:p.Gly216Val
ENST00000688927.1:n.2858G>T
ENST00000689283.1:c.*310G>T	ENSP00000509050.1:n.*310G>T
ENST00000689477.1:c.*540G>T	ENSP00000508945.1:n.*540G>T
ENST00000689765.1:c.*169-29G>T	ENSP00000509625.1:n.*169-29G>T
ENST00000690512.1:c.*498G>T	ENSP00000509793.1:n.*498G>T
ENST00000692039.1:c.*445G>T	ENSP00000508821.1:n.*445G>T
ENST00000692336.1:c.671G>T	ENSP00000508540.1:p.Gly224Val
ENST00000693133.1:n.1127G>T
ENST00000263578.10:c.647G>T MANE Select	ENSP00000263578.5:p.Gly216Val
ENST00000263578.9:c.647G>T	ENSP00000263578.5:p.Gly216Val
ENST00000524751.5:n.888G>T
ENST00000525083.5:n.367G>T
ENST00000525770.5:c.*279G>T	ENSP00000434739.1:n.*279G>T
ENST00000527004.5:c.549G>T	ENSP00000436374.1:p.Arg183Ser
ENST00000530642.1:n.1429G>T
ENST00000532101.5:n.870G>T
ENST00000532125.1:c.605G>T	ENSP00000434178.1:p.Gly202Val
ENST00000533395.5:n.380G>T
ENST00000533839.5:n.238-452G>T
ENST00000534011.5:n.699G>T
ENST00000534315.5:n.959G>T
NM_017547.3:c.647G>T	NP_060017.1:p.Gly216Val
NR_037647.1:n.593G>T
NR_037648.1:n.833G>T
XM_006718879.2:c.137G>T	XP_006718942.1:p.Gly46Val
XM_006718880.2:c.14G>T	XP_006718943.1:p.Gly5Val
XM_006718881.2:c.14G>T	XP_006718944.1:p.Gly5Val
XM_011542895.1:c.137G>T	XP_011541197.1:p.Gly46Val
XM_011542896.1:c.137G>T	XP_011541198.1:p.Gly46Val
XM_006718879.3:c.137G>T	XP_006718942.1:p.Gly46Val
XM_006718881.3:c.14G>T	XP_006718944.1:p.Gly5Val
XM_011542895.2:c.137G>T	XP_011541197.1:p.Gly46Val
XM_011542896.2:c.137G>T	XP_011541198.1:p.Gly46Val
XM_017018000.2:c.647G>T	XP_016873489.1:p.Gly216Val
XM_017018001.1:c.137G>T	XP_016873490.1:p.Gly46Val
XM_017018002.1:c.137G>T	XP_016873491.1:p.Gly46Val
XM_017018003.2:c.14G>T	XP_016873492.1:p.Gly5Val
XM_017018004.1:c.14G>T	XP_016873493.1:p.Gly5Val
XM_017018005.1:c.14G>T	XP_016873494.1:p.Gly5Val
XM_017018006.2:c.14G>T	XP_016873495.1:p.Gly5Val
NM_017547.4:c.647G>T MANE Select	NP_060017.1:p.Gly216Val
NR_037647.2:n.479G>T
NR_037648.2:n.824G>T