Canonical Allele Identifier: CA477516067

Gene: FOXRED1

Linked Data

• ClinVar Variation Id: 2748679
• ClinVar RCV Id: RCV003566096
• gnomAD v4: 11-126275367-C-T
• MyVariant Identifiers: chr11:g.126145262C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275367C>T , CM000673.2:g.126275367C>T	GRCh38
NC_000011.9:g.126145262C>T , CM000673.1:g.126145262C>T	GRCh37
NC_000011.8:g.125650472C>T	NCBI36
NG_028029.1:g.11328C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1155C>T
ENST00000532101.6:n.774C>T
ENST00000532125.2:c.669C>T	ENSP00000434178.2:p.Leu223=
ENST00000533839.6:c.86-427C>T	ENSP00000509952.1:n.86-427C>T
ENST00000534011.6:n.964C>T
ENST00000685484.1:c.672C>T	ENSP00000510622.1:p.Leu224=
ENST00000685601.1:c.672C>T	ENSP00000510603.1:p.Leu224=
ENST00000685765.1:c.672C>T	ENSP00000509991.1:p.Leu224=
ENST00000685844.1:c.*209C>T	ENSP00000509820.1:n.*209C>T
ENST00000685857.1:n.1411C>T
ENST00000686242.1:c.471C>T	ENSP00000508950.1:n.471C>T
ENST00000686888.1:c.*239C>T	ENSP00000509619.1:n.*239C>T
ENST00000687699.1:c.796C>T	ENSP00000508878.1:n.796C>T
ENST00000687786.1:n.2108C>T
ENST00000688100.1:n.1593C>T
ENST00000688588.1:c.672C>T	ENSP00000510802.1:p.Leu224=
ENST00000688927.1:n.2883C>T
ENST00000689283.1:c.*335C>T	ENSP00000509050.1:n.*335C>T
ENST00000689477.1:c.*565C>T	ENSP00000508945.1:n.*565C>T
ENST00000689765.1:c.*169-4C>T	ENSP00000509625.1:n.*169-4C>T
ENST00000690512.1:c.*523C>T	ENSP00000509793.1:n.*523C>T
ENST00000692039.1:c.*470C>T	ENSP00000508821.1:n.*470C>T
ENST00000692336.1:c.696C>T	ENSP00000508540.1:p.Leu232=
ENST00000693133.1:n.1152C>T
ENST00000263578.10:c.672C>T MANE Select	ENSP00000263578.5:p.Leu224=
ENST00000263578.9:c.672C>T	ENSP00000263578.5:p.Leu224=
ENST00000525083.5:n.392C>T
ENST00000525770.5:c.*304C>T	ENSP00000434739.1:n.*304C>T
ENST00000527004.5:c.*16C>T	ENSP00000436374.1:n.*16C>T
ENST00000530642.1:n.1454C>T
ENST00000532101.5:n.895C>T
ENST00000532125.1:c.630C>T	ENSP00000434178.1:p.Leu210=
ENST00000533395.5:n.405C>T
ENST00000533839.5:n.238-427C>T
ENST00000534011.5:n.724C>T
ENST00000534315.5:n.984C>T
NM_017547.3:c.672C>T	NP_060017.1:p.Leu224=
NR_037647.1:n.618C>T
NR_037648.1:n.858C>T
XM_006718879.2:c.162C>T	XP_006718942.1:p.Leu54=
XM_006718880.2:c.39C>T	XP_006718943.1:p.Leu13=
XM_006718881.2:c.39C>T	XP_006718944.1:p.Leu13=
XM_011542895.1:c.162C>T	XP_011541197.1:p.Leu54=
XM_011542896.1:c.162C>T	XP_011541198.1:p.Leu54=
XM_006718879.3:c.162C>T	XP_006718942.1:p.Leu54=
XM_006718881.3:c.39C>T	XP_006718944.1:p.Leu13=
XM_011542895.2:c.162C>T	XP_011541197.1:p.Leu54=
XM_011542896.2:c.162C>T	XP_011541198.1:p.Leu54=
XM_017018000.2:c.672C>T	XP_016873489.1:p.Leu224=
XM_017018001.1:c.162C>T	XP_016873490.1:p.Leu54=
XM_017018002.1:c.162C>T	XP_016873491.1:p.Leu54=
XM_017018003.2:c.39C>T	XP_016873492.1:p.Leu13=
XM_017018004.1:c.39C>T	XP_016873493.1:p.Leu13=
XM_017018005.1:c.39C>T	XP_016873494.1:p.Leu13=
XM_017018006.2:c.39C>T	XP_016873495.1:p.Leu13=
NM_017547.4:c.672C>T MANE Select	NP_060017.1:p.Leu224=
NR_037647.2:n.504C>T
NR_037648.2:n.849C>T