Canonical Allele Identifier: CA6354169

Gene: FOXRED1

Linked Data

• dbSNP Id: rs780522584
• ExAC: 11:126145246 A / AC
• gnomAD v2: 11-126145246-A-AC
• MyVariant Identifiers: chr11:g.126145246_126145247insC (hg19) ; chr11:g.126275351_126275352insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275355dup , CM000673.2:g.126275355dup	GRCh38
NC_000011.9:g.126145250dup , CM000673.1:g.126145250dup	GRCh37
NC_000011.8:g.125650460dup	NCBI36
NG_028029.1:g.11316dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1143dup
ENST00000532101.6:n.762dup
ENST00000532125.2:c.657dup	ENSP00000434178.2:p.Trp220LeufsTer?
ENST00000533839.6:c.86-439dup	ENSP00000509952.1:n.86-439dup
ENST00000534011.6:n.952dup
ENST00000685484.1:c.660dup	ENSP00000510622.1:p.Trp221LeufsTer?
ENST00000685601.1:c.660dup	ENSP00000510603.1:p.Trp221LeufsTer?
ENST00000685765.1:c.660dup	ENSP00000509991.1:p.Trp221LeufsTer?
ENST00000685844.1:c.*197dup	ENSP00000509820.1:n.*197dup
ENST00000685857.1:n.1399dup
ENST00000686242.1:c.459dup	ENSP00000508950.1:n.459dup
ENST00000686888.1:c.*227dup	ENSP00000509619.1:n.*227dup
ENST00000687699.1:c.784dup	ENSP00000508878.1:n.784dup
ENST00000687786.1:n.2096dup
ENST00000688100.1:n.1581dup
ENST00000688588.1:c.660dup	ENSP00000510802.1:p.Trp221LeufsTer?
ENST00000688927.1:n.2871dup
ENST00000689283.1:c.*323dup	ENSP00000509050.1:n.*323dup
ENST00000689477.1:c.*553dup	ENSP00000508945.1:n.*553dup
ENST00000689765.1:c.*169-16dup	ENSP00000509625.1:n.*169-16dup
ENST00000690512.1:c.*511dup	ENSP00000509793.1:n.*511dup
ENST00000692039.1:c.*458dup	ENSP00000508821.1:n.*458dup
ENST00000692336.1:c.684dup	ENSP00000508540.1:p.Trp229LeufsTer?
ENST00000693133.1:n.1140dup
ENST00000263578.10:c.660dup MANE Select	ENSP00000263578.5:p.Trp221LeufsTer?
ENST00000263578.9:c.660dup	ENSP00000263578.5:p.Trp221LeufsTer?
ENST00000525083.5:n.380dup
ENST00000525770.5:c.*292dup	ENSP00000434739.1:n.*292dup
ENST00000527004.5:c.*4dup	ENSP00000436374.1:n.*4dup
ENST00000530642.1:n.1442dup
ENST00000532101.5:n.883dup
ENST00000532125.1:c.618dup	ENSP00000434178.1:p.Trp207LeufsTer?
ENST00000533395.5:n.393dup
ENST00000533839.5:n.238-439dup
ENST00000534011.5:n.712dup
ENST00000534315.5:n.972dup
NM_017547.3:c.660dup	NP_060017.1:p.Trp221LeufsTer?
NR_037647.1:n.606dup
NR_037648.1:n.846dup
XM_006718879.2:c.150dup	XP_006718942.1:p.Trp51LeufsTer?
XM_006718880.2:c.27dup	XP_006718943.1:p.Trp10LeufsTer?
XM_006718881.2:c.27dup	XP_006718944.1:p.Trp10LeufsTer?
XM_011542895.1:c.150dup	XP_011541197.1:p.Trp51LeufsTer?
XM_011542896.1:c.150dup	XP_011541198.1:p.Trp51LeufsTer?
XM_006718879.3:c.150dup	XP_006718942.1:p.Trp51LeufsTer?
XM_006718881.3:c.27dup	XP_006718944.1:p.Trp10LeufsTer?
XM_011542895.2:c.150dup	XP_011541197.1:p.Trp51LeufsTer?
XM_011542896.2:c.150dup	XP_011541198.1:p.Trp51LeufsTer?
XM_017018000.2:c.660dup	XP_016873489.1:p.Trp221LeufsTer?
XM_017018001.1:c.150dup	XP_016873490.1:p.Trp51LeufsTer?
XM_017018002.1:c.150dup	XP_016873491.1:p.Trp51LeufsTer?
XM_017018003.2:c.27dup	XP_016873492.1:p.Trp10LeufsTer?
XM_017018004.1:c.27dup	XP_016873493.1:p.Trp10LeufsTer?
XM_017018005.1:c.27dup	XP_016873494.1:p.Trp10LeufsTer?
XM_017018006.2:c.27dup	XP_016873495.1:p.Trp10LeufsTer?
NM_017547.4:c.660dup MANE Select	NP_060017.1:p.Trp221LeufsTer?
NR_037647.2:n.492dup
NR_037648.2:n.837dup