Canonical Allele Identifier: CA383230116

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145241G>T (hg19) ; chr11:g.126275346G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275346G>T , CM000673.2:g.126275346G>T	GRCh38
NC_000011.9:g.126145241G>T , CM000673.1:g.126145241G>T	GRCh37
NC_000011.8:g.125650451G>T	NCBI36
NG_028029.1:g.11307G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1134G>T
ENST00000532101.6:n.753G>T
ENST00000532125.2:c.648G>T	ENSP00000434178.2:p.Trp216Cys
ENST00000533839.6:c.86-448G>T	ENSP00000509952.1:n.86-448G>T
ENST00000534011.6:n.943G>T
ENST00000685484.1:c.651G>T	ENSP00000510622.1:p.Trp217Cys
ENST00000685601.1:c.651G>T	ENSP00000510603.1:p.Trp217Cys
ENST00000685765.1:c.651G>T	ENSP00000509991.1:p.Trp217Cys
ENST00000685844.1:c.*188G>T	ENSP00000509820.1:n.*188G>T
ENST00000685857.1:n.1390G>T
ENST00000686242.1:c.450G>T	ENSP00000508950.1:n.450G>T
ENST00000686888.1:c.*218G>T	ENSP00000509619.1:n.*218G>T
ENST00000687699.1:c.775G>T	ENSP00000508878.1:n.775G>T
ENST00000687786.1:n.2087G>T
ENST00000688100.1:n.1572G>T
ENST00000688588.1:c.651G>T	ENSP00000510802.1:p.Trp217Cys
ENST00000688927.1:n.2862G>T
ENST00000689283.1:c.*314G>T	ENSP00000509050.1:n.*314G>T
ENST00000689477.1:c.*544G>T	ENSP00000508945.1:n.*544G>T
ENST00000689765.1:c.*169-25G>T	ENSP00000509625.1:n.*169-25G>T
ENST00000690512.1:c.*502G>T	ENSP00000509793.1:n.*502G>T
ENST00000692039.1:c.*449G>T	ENSP00000508821.1:n.*449G>T
ENST00000692336.1:c.675G>T	ENSP00000508540.1:p.Trp225Cys
ENST00000693133.1:n.1131G>T
ENST00000263578.10:c.651G>T MANE Select	ENSP00000263578.5:p.Trp217Cys
ENST00000263578.9:c.651G>T	ENSP00000263578.5:p.Trp217Cys
ENST00000524751.5:n.892G>T
ENST00000525083.5:n.371G>T
ENST00000525770.5:c.*283G>T	ENSP00000434739.1:n.*283G>T
ENST00000527004.5:c.553G>T	ENSP00000436374.1:p.Val185Phe
ENST00000530642.1:n.1433G>T
ENST00000532101.5:n.874G>T
ENST00000532125.1:c.609G>T	ENSP00000434178.1:p.Trp203Cys
ENST00000533395.5:n.384G>T
ENST00000533839.5:n.238-448G>T
ENST00000534011.5:n.703G>T
ENST00000534315.5:n.963G>T
NM_017547.3:c.651G>T	NP_060017.1:p.Trp217Cys
NR_037647.1:n.597G>T
NR_037648.1:n.837G>T
XM_006718879.2:c.141G>T	XP_006718942.1:p.Trp47Cys
XM_006718880.2:c.18G>T	XP_006718943.1:p.Trp6Cys
XM_006718881.2:c.18G>T	XP_006718944.1:p.Trp6Cys
XM_011542895.1:c.141G>T	XP_011541197.1:p.Trp47Cys
XM_011542896.1:c.141G>T	XP_011541198.1:p.Trp47Cys
XM_006718879.3:c.141G>T	XP_006718942.1:p.Trp47Cys
XM_006718881.3:c.18G>T	XP_006718944.1:p.Trp6Cys
XM_011542895.2:c.141G>T	XP_011541197.1:p.Trp47Cys
XM_011542896.2:c.141G>T	XP_011541198.1:p.Trp47Cys
XM_017018000.2:c.651G>T	XP_016873489.1:p.Trp217Cys
XM_017018001.1:c.141G>T	XP_016873490.1:p.Trp47Cys
XM_017018002.1:c.141G>T	XP_016873491.1:p.Trp47Cys
XM_017018003.2:c.18G>T	XP_016873492.1:p.Trp6Cys
XM_017018004.1:c.18G>T	XP_016873493.1:p.Trp6Cys
XM_017018005.1:c.18G>T	XP_016873494.1:p.Trp6Cys
XM_017018006.2:c.18G>T	XP_016873495.1:p.Trp6Cys
NM_017547.4:c.651G>T MANE Select	NP_060017.1:p.Trp217Cys
NR_037647.2:n.483G>T
NR_037648.2:n.828G>T