Canonical Allele Identifier: CA383230276

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145317G>T (hg19) ; chr11:g.126275422G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275422G>T , CM000673.2:g.126275422G>T	GRCh38
NC_000011.9:g.126145317G>T , CM000673.1:g.126145317G>T	GRCh37
NC_000011.8:g.125650527G>T	NCBI36
NG_028029.1:g.11383G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1210G>T
ENST00000532101.6:n.829G>T
ENST00000532125.2:c.724G>T	ENSP00000434178.2:p.Val242Leu
ENST00000533839.6:c.86-372G>T	ENSP00000509952.1:n.86-372G>T
ENST00000534011.6:n.1019G>T
ENST00000685484.1:c.727G>T	ENSP00000510622.1:p.Val243Leu
ENST00000685601.1:c.727G>T	ENSP00000510603.1:p.Val243Leu
ENST00000685765.1:c.727G>T	ENSP00000509991.1:p.Val243Leu
ENST00000685844.1:c.*264G>T	ENSP00000509820.1:n.*264G>T
ENST00000685857.1:n.1466G>T
ENST00000686242.1:c.526G>T	ENSP00000508950.1:n.526G>T
ENST00000686888.1:c.*294G>T	ENSP00000509619.1:n.*294G>T
ENST00000687699.1:c.851G>T	ENSP00000508878.1:n.851G>T
ENST00000687786.1:n.2163G>T
ENST00000688100.1:n.1648G>T
ENST00000688588.1:c.727G>T	ENSP00000510802.1:p.Val243Leu
ENST00000688927.1:n.2938G>T
ENST00000689283.1:c.*390G>T	ENSP00000509050.1:n.*390G>T
ENST00000689477.1:c.*620G>T	ENSP00000508945.1:n.*620G>T
ENST00000689765.1:c.*220G>T	ENSP00000509625.1:n.*220G>T
ENST00000690512.1:c.*578G>T	ENSP00000509793.1:n.*578G>T
ENST00000692039.1:c.*525G>T	ENSP00000508821.1:n.*525G>T
ENST00000692336.1:c.751G>T	ENSP00000508540.1:p.Val251Leu
ENST00000693133.1:n.1207G>T
ENST00000263578.10:c.727G>T MANE Select	ENSP00000263578.5:p.Val243Leu
ENST00000263578.9:c.727G>T	ENSP00000263578.5:p.Val243Leu
ENST00000525083.5:n.447G>T
ENST00000525770.5:c.*359G>T	ENSP00000434739.1:n.*359G>T
ENST00000527004.5:c.*71G>T	ENSP00000436374.1:n.*71G>T
ENST00000530642.1:n.1509G>T
ENST00000532101.5:n.950G>T
ENST00000532125.1:c.685G>T	ENSP00000434178.1:p.Val229Leu
ENST00000533395.5:n.460G>T
ENST00000533839.5:n.238-372G>T
ENST00000534011.5:n.779G>T
ENST00000534315.5:n.1039G>T
NM_017547.3:c.727G>T	NP_060017.1:p.Val243Leu
NR_037647.1:n.673G>T
NR_037648.1:n.913G>T
XM_006718879.2:c.217G>T	XP_006718942.1:p.Val73Leu
XM_006718880.2:c.94G>T	XP_006718943.1:p.Val32Leu
XM_006718881.2:c.94G>T	XP_006718944.1:p.Val32Leu
XM_011542895.1:c.217G>T	XP_011541197.1:p.Val73Leu
XM_011542896.1:c.217G>T	XP_011541198.1:p.Val73Leu
XM_006718879.3:c.217G>T	XP_006718942.1:p.Val73Leu
XM_006718881.3:c.94G>T	XP_006718944.1:p.Val32Leu
XM_011542895.2:c.217G>T	XP_011541197.1:p.Val73Leu
XM_011542896.2:c.217G>T	XP_011541198.1:p.Val73Leu
XM_017018000.2:c.727G>T	XP_016873489.1:p.Val243Leu
XM_017018001.1:c.217G>T	XP_016873490.1:p.Val73Leu
XM_017018002.1:c.217G>T	XP_016873491.1:p.Val73Leu
XM_017018003.2:c.94G>T	XP_016873492.1:p.Val32Leu
XM_017018004.1:c.94G>T	XP_016873493.1:p.Val32Leu
XM_017018005.1:c.94G>T	XP_016873494.1:p.Val32Leu
XM_017018006.2:c.94G>T	XP_016873495.1:p.Val32Leu
NM_017547.4:c.727G>T MANE Select	NP_060017.1:p.Val243Leu
NR_037647.2:n.559G>T
NR_037648.2:n.904G>T