Canonical Allele Identifier: CA383230138

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145251T>A (hg19) ; chr11:g.126275356T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275356T>A , CM000673.2:g.126275356T>A	GRCh38
NC_000011.9:g.126145251T>A , CM000673.1:g.126145251T>A	GRCh37
NC_000011.8:g.125650461T>A	NCBI36
NG_028029.1:g.11317T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1144T>A
ENST00000532101.6:n.763T>A
ENST00000532125.2:c.658T>A	ENSP00000434178.2:p.Trp220Arg
ENST00000533839.6:c.86-438T>A	ENSP00000509952.1:n.86-438T>A
ENST00000534011.6:n.953T>A
ENST00000685484.1:c.661T>A	ENSP00000510622.1:p.Trp221Arg
ENST00000685601.1:c.661T>A	ENSP00000510603.1:p.Trp221Arg
ENST00000685765.1:c.661T>A	ENSP00000509991.1:p.Trp221Arg
ENST00000685844.1:c.*198T>A	ENSP00000509820.1:n.*198T>A
ENST00000685857.1:n.1400T>A
ENST00000686242.1:c.460T>A	ENSP00000508950.1:n.460T>A
ENST00000686888.1:c.*228T>A	ENSP00000509619.1:n.*228T>A
ENST00000687699.1:c.785T>A	ENSP00000508878.1:n.785T>A
ENST00000687786.1:n.2097T>A
ENST00000688100.1:n.1582T>A
ENST00000688588.1:c.661T>A	ENSP00000510802.1:p.Trp221Arg
ENST00000688927.1:n.2872T>A
ENST00000689283.1:c.*324T>A	ENSP00000509050.1:n.*324T>A
ENST00000689477.1:c.*554T>A	ENSP00000508945.1:n.*554T>A
ENST00000689765.1:c.*169-15T>A	ENSP00000509625.1:n.*169-15T>A
ENST00000690512.1:c.*512T>A	ENSP00000509793.1:n.*512T>A
ENST00000692039.1:c.*459T>A	ENSP00000508821.1:n.*459T>A
ENST00000692336.1:c.685T>A	ENSP00000508540.1:p.Trp229Arg
ENST00000693133.1:n.1141T>A
ENST00000263578.10:c.661T>A MANE Select	ENSP00000263578.5:p.Trp221Arg
ENST00000263578.9:c.661T>A	ENSP00000263578.5:p.Trp221Arg
ENST00000525083.5:n.381T>A
ENST00000525770.5:c.*293T>A	ENSP00000434739.1:n.*293T>A
ENST00000527004.5:c.*5T>A	ENSP00000436374.1:n.*5T>A
ENST00000530642.1:n.1443T>A
ENST00000532101.5:n.884T>A
ENST00000532125.1:c.619T>A	ENSP00000434178.1:p.Trp207Arg
ENST00000533395.5:n.394T>A
ENST00000533839.5:n.238-438T>A
ENST00000534011.5:n.713T>A
ENST00000534315.5:n.973T>A
NM_017547.3:c.661T>A	NP_060017.1:p.Trp221Arg
NR_037647.1:n.607T>A
NR_037648.1:n.847T>A
XM_006718879.2:c.151T>A	XP_006718942.1:p.Trp51Arg
XM_006718880.2:c.28T>A	XP_006718943.1:p.Trp10Arg
XM_006718881.2:c.28T>A	XP_006718944.1:p.Trp10Arg
XM_011542895.1:c.151T>A	XP_011541197.1:p.Trp51Arg
XM_011542896.1:c.151T>A	XP_011541198.1:p.Trp51Arg
XM_006718879.3:c.151T>A	XP_006718942.1:p.Trp51Arg
XM_006718881.3:c.28T>A	XP_006718944.1:p.Trp10Arg
XM_011542895.2:c.151T>A	XP_011541197.1:p.Trp51Arg
XM_011542896.2:c.151T>A	XP_011541198.1:p.Trp51Arg
XM_017018000.2:c.661T>A	XP_016873489.1:p.Trp221Arg
XM_017018001.1:c.151T>A	XP_016873490.1:p.Trp51Arg
XM_017018002.1:c.151T>A	XP_016873491.1:p.Trp51Arg
XM_017018003.2:c.28T>A	XP_016873492.1:p.Trp10Arg
XM_017018004.1:c.28T>A	XP_016873493.1:p.Trp10Arg
XM_017018005.1:c.28T>A	XP_016873494.1:p.Trp10Arg
XM_017018006.2:c.28T>A	XP_016873495.1:p.Trp10Arg
NM_017547.4:c.661T>A MANE Select	NP_060017.1:p.Trp221Arg
NR_037647.2:n.493T>A
NR_037648.2:n.838T>A