Canonical Allele Identifier: CA477513817

Gene: FOXRED1

Linked Data

• ClinVar Variation Id: 2859800
• ClinVar RCV Id: RCV003702011
• dbSNP Id: rs1164602988
• MyVariant Identifiers: chr11:g.126141531A>C (hg19) ; chr11:g.126271636A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126271636A>C , CM000673.2:g.126271636A>C	GRCh38
NC_000011.9:g.126141531A>C , CM000673.1:g.126141531A>C	GRCh37
NC_000011.8:g.125646741A>C	NCBI36
NG_028029.1:g.7597A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.463A>C
ENST00000532101.6:n.462A>C
ENST00000532125.2:c.285A>C	ENSP00000434178.2:p.Leu95=
ENST00000533839.6:c.85+2345A>C	ENSP00000509952.1:n.85+2345A>C
ENST00000534011.6:n.561A>C
ENST00000685484.1:c.285A>C	ENSP00000510622.1:p.Leu95=
ENST00000685601.1:c.285A>C	ENSP00000510603.1:p.Leu95=
ENST00000685765.1:c.285A>C	ENSP00000509991.1:p.Leu95=
ENST00000685844.1:c.86-1333A>C	ENSP00000509820.1:n.86-1333A>C
ENST00000685857.1:n.463A>C
ENST00000686242.1:c.86-1333A>C	ENSP00000508950.1:n.86-1333A>C
ENST00000686888.1:c.285A>C	ENSP00000509619.1:p.Leu95=
ENST00000687699.1:c.409A>C	ENSP00000508878.1:n.409A>C
ENST00000687786.1:n.1618A>C
ENST00000688588.1:c.285A>C	ENSP00000510802.1:p.Leu95=
ENST00000688927.1:n.463A>C
ENST00000689283.1:c.210-1333A>C	ENSP00000509050.1:n.210-1333A>C
ENST00000689477.1:c.*178A>C	ENSP00000508945.1:n.*178A>C
ENST00000689765.1:c.86-1333A>C	ENSP00000509625.1:n.86-1333A>C
ENST00000690512.1:c.86-842A>C	ENSP00000509793.1:n.86-842A>C
ENST00000692039.1:c.*83A>C	ENSP00000508821.1:n.*83A>C
ENST00000692336.1:c.285A>C	ENSP00000508540.1:p.Leu95=
ENST00000693133.1:n.226-1333A>C
ENST00000263578.10:c.285A>C MANE Select	ENSP00000263578.5:p.Leu95=
ENST00000263578.9:c.285A>C	ENSP00000263578.5:p.Leu95=
ENST00000524751.5:n.223-1333A>C
ENST00000525083.5:n.122-1333A>C
ENST00000525770.5:c.86-1333A>C	ENSP00000434739.1:n.86-1333A>C
ENST00000526366.5:n.101-83A>C
ENST00000526525.1:n.246-1333A>C
ENST00000527004.5:c.285A>C	ENSP00000436374.1:p.Leu95=
ENST00000529802.1:n.335A>C
ENST00000532101.5:n.508A>C
ENST00000532125.1:c.243A>C	ENSP00000434178.1:p.Leu81=
ENST00000533839.5:n.237+2345A>C
ENST00000534011.5:n.158-842A>C
ENST00000534315.5:n.692A>C
NM_017547.3:c.285A>C	NP_060017.1:p.Leu95=
NR_037647.1:n.253-1333A>C
NR_037648.1:n.471A>C
XM_006718880.2:c.-254A>C	XP_006718943.1:n.-254A>C
XM_006718881.2:c.-232-1333A>C	XP_006718944.1:n.-232-1333A>C
XM_011542895.1:c.-226A>C	XP_011541197.1:n.-226A>C
XM_011542896.1:c.-246A>C	XP_011541198.1:n.-246A>C
XM_006718881.3:c.-232-1333A>C	XP_006718944.1:n.-232-1333A>C
XM_011542895.2:c.-226A>C	XP_011541197.1:n.-226A>C
XM_011542896.2:c.-246A>C	XP_011541198.1:n.-246A>C
XM_017018000.2:c.285A>C	XP_016873489.1:p.Leu95=
XM_017018001.1:c.-246A>C	XP_016873490.1:n.-246A>C
XM_017018002.1:c.-224-1333A>C	XP_016873491.1:n.-224-1333A>C
XM_017018003.2:c.-254A>C	XP_016873492.1:n.-254A>C
XM_017018004.1:c.-254A>C	XP_016873493.1:n.-254A>C
XM_017018005.1:c.-452A>C	XP_016873494.1:n.-452A>C
XM_017018006.2:c.-254A>C	XP_016873495.1:n.-254A>C
NM_017547.4:c.285A>C MANE Select	NP_060017.1:p.Leu95=
NR_037647.2:n.139-1333A>C
NR_037648.2:n.462A>C