Canonical Allele Identifier: CA383229898

Gene: FOXRED1

Linked Data

• dbSNP Id: rs1203498243
• gnomAD v2: 11-126144844-C-A
• gnomAD v3: 11-126274949-C-A
• gnomAD v4: 11-126274949-C-A
• MyVariant Identifiers: chr11:g.126144844C>A (hg19) ; chr11:g.126274949C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274949C>A , CM000673.2:g.126274949C>A	GRCh38
NC_000011.9:g.126144844C>A , CM000673.1:g.126144844C>A	GRCh37
NC_000011.8:g.125650054C>A	NCBI36
NG_028029.1:g.10910C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.737C>A
ENST00000532101.6:n.734-378C>A
ENST00000532125.2:c.556C>A	ENSP00000434178.2:p.Leu186Met
ENST00000533839.6:c.86-845C>A	ENSP00000509952.1:n.86-845C>A
ENST00000534011.6:n.851C>A
ENST00000685484.1:c.559C>A	ENSP00000510622.1:p.Leu187Met
ENST00000685601.1:c.559C>A	ENSP00000510603.1:p.Leu187Met
ENST00000685765.1:c.559C>A	ENSP00000509991.1:p.Leu187Met
ENST00000685844.1:c.*169-378C>A	ENSP00000509820.1:n.*169-378C>A
ENST00000685857.1:n.993C>A
ENST00000686242.1:c.358C>A	ENSP00000508950.1:n.358C>A
ENST00000686888.1:c.*126C>A	ENSP00000509619.1:n.*126C>A
ENST00000687699.1:c.683C>A	ENSP00000508878.1:n.683C>A
ENST00000687786.1:n.2068-378C>A
ENST00000688100.1:n.1480C>A
ENST00000688588.1:c.559C>A	ENSP00000510802.1:p.Leu187Met
ENST00000688927.1:n.2465C>A
ENST00000689283.1:c.*222C>A	ENSP00000509050.1:n.*222C>A
ENST00000689477.1:c.*452C>A	ENSP00000508945.1:n.*452C>A
ENST00000689765.1:c.*169-422C>A	ENSP00000509625.1:n.*169-422C>A
ENST00000690512.1:c.*410C>A	ENSP00000509793.1:n.*410C>A
ENST00000692039.1:c.*357C>A	ENSP00000508821.1:n.*357C>A
ENST00000692336.1:c.583C>A	ENSP00000508540.1:p.Leu195Met
ENST00000693133.1:n.734C>A
ENST00000263578.10:c.559C>A MANE Select	ENSP00000263578.5:p.Leu187Met
ENST00000263578.9:c.559C>A	ENSP00000263578.5:p.Leu187Met
ENST00000524751.5:n.495C>A
ENST00000525083.5:n.352-378C>A
ENST00000525770.5:c.*191C>A	ENSP00000434739.1:n.*191C>A
ENST00000526366.5:n.490C>A
ENST00000527004.5:c.534-378C>A	ENSP00000436374.1:n.534-378C>A
ENST00000527875.1:n.389C>A
ENST00000530642.1:n.1036C>A
ENST00000532101.5:n.782C>A
ENST00000532125.1:c.517C>A	ENSP00000434178.1:p.Leu173Met
ENST00000533395.5:n.365-378C>A
ENST00000533839.5:n.238-845C>A
ENST00000534011.5:n.611C>A
ENST00000534315.5:n.944-378C>A
NM_017547.3:c.559C>A	NP_060017.1:p.Leu187Met
NR_037647.1:n.505C>A
NR_037648.1:n.745C>A
XM_006718879.2:c.49C>A	XP_006718942.1:p.Leu17Met
XM_006718880.2:c.-2-378C>A	XP_006718943.1:n.-2-378C>A
XM_006718881.2:c.-2-378C>A	XP_006718944.1:n.-2-378C>A
XM_011542895.1:c.49C>A	XP_011541197.1:p.Leu17Met
XM_011542896.1:c.49C>A	XP_011541198.1:p.Leu17Met
XM_006718879.3:c.49C>A	XP_006718942.1:p.Leu17Met
XM_006718881.3:c.-2-378C>A	XP_006718944.1:n.-2-378C>A
XM_011542895.2:c.49C>A	XP_011541197.1:p.Leu17Met
XM_011542896.2:c.49C>A	XP_011541198.1:p.Leu17Met
XM_017018000.2:c.559C>A	XP_016873489.1:p.Leu187Met
XM_017018001.1:c.49C>A	XP_016873490.1:p.Leu17Met
XM_017018002.1:c.49C>A	XP_016873491.1:p.Leu17Met
XM_017018003.2:c.-2-378C>A	XP_016873492.1:n.-2-378C>A
XM_017018004.1:c.-2-378C>A	XP_016873493.1:n.-2-378C>A
XM_017018005.1:c.-2-378C>A	XP_016873494.1:n.-2-378C>A
XM_017018006.2:c.-2-378C>A	XP_016873495.1:n.-2-378C>A
NM_017547.4:c.559C>A MANE Select	NP_060017.1:p.Leu187Met
NR_037647.2:n.391C>A
NR_037648.2:n.736C>A