Canonical Allele Identifier: CA383229108

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126141440A>C (hg19) ; chr11:g.126271545A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126271545A>C , CM000673.2:g.126271545A>C	GRCh38
NC_000011.9:g.126141440A>C , CM000673.1:g.126141440A>C	GRCh37
NC_000011.8:g.125646650A>C	NCBI36
NG_028029.1:g.7506A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.372A>C
ENST00000532101.6:n.371A>C
ENST00000532125.2:c.194A>C	ENSP00000434178.2:p.Asp65Ala
ENST00000533839.6:c.85+2254A>C	ENSP00000509952.1:n.85+2254A>C
ENST00000534011.6:n.470A>C
ENST00000685484.1:c.194A>C	ENSP00000510622.1:p.Asp65Ala
ENST00000685601.1:c.194A>C	ENSP00000510603.1:p.Asp65Ala
ENST00000685765.1:c.194A>C	ENSP00000509991.1:p.Asp65Ala
ENST00000685844.1:c.86-1424A>C	ENSP00000509820.1:n.86-1424A>C
ENST00000685857.1:n.372A>C
ENST00000686242.1:c.86-1424A>C	ENSP00000508950.1:n.86-1424A>C
ENST00000686888.1:c.194A>C	ENSP00000509619.1:p.Asp65Ala
ENST00000687699.1:c.318A>C	ENSP00000508878.1:n.318A>C
ENST00000687786.1:n.1527A>C
ENST00000688588.1:c.194A>C	ENSP00000510802.1:p.Asp65Ala
ENST00000688927.1:n.372A>C
ENST00000689283.1:c.210-1424A>C	ENSP00000509050.1:n.210-1424A>C
ENST00000689477.1:c.*87A>C	ENSP00000508945.1:n.*87A>C
ENST00000689765.1:c.86-1424A>C	ENSP00000509625.1:n.86-1424A>C
ENST00000690512.1:c.86-933A>C	ENSP00000509793.1:n.86-933A>C
ENST00000692039.1:c.280A>C	ENSP00000508821.1:p.Met94Leu
ENST00000692336.1:c.194A>C	ENSP00000508540.1:p.Asp65Ala
ENST00000693133.1:n.226-1424A>C
ENST00000263578.10:c.194A>C MANE Select	ENSP00000263578.5:p.Asp65Ala
ENST00000263578.9:c.194A>C	ENSP00000263578.5:p.Asp65Ala
ENST00000524751.5:n.223-1424A>C
ENST00000525083.5:n.122-1424A>C
ENST00000525770.5:c.86-1424A>C	ENSP00000434739.1:n.86-1424A>C
ENST00000526366.5:n.101-174A>C
ENST00000526525.1:n.246-1424A>C
ENST00000527004.5:c.194A>C	ENSP00000436374.1:p.Asp65Ala
ENST00000529802.1:n.244A>C
ENST00000532101.5:n.417A>C
ENST00000532125.1:c.152A>C	ENSP00000434178.1:p.Asp51Ala
ENST00000533839.5:n.237+2254A>C
ENST00000534011.5:n.158-933A>C
ENST00000534315.5:n.601A>C
NM_017547.3:c.194A>C	NP_060017.1:p.Asp65Ala
NR_037647.1:n.253-1424A>C
NR_037648.1:n.380A>C
XM_006718880.2:c.-345A>C	XP_006718943.1:n.-345A>C
XM_006718881.2:c.-232-1424A>C	XP_006718944.1:n.-232-1424A>C
XM_011542895.1:c.-317A>C	XP_011541197.1:n.-317A>C
XM_011542896.1:c.-337A>C	XP_011541198.1:n.-337A>C
XM_006718881.3:c.-232-1424A>C	XP_006718944.1:n.-232-1424A>C
XM_011542895.2:c.-317A>C	XP_011541197.1:n.-317A>C
XM_011542896.2:c.-337A>C	XP_011541198.1:n.-337A>C
XM_017018000.2:c.194A>C	XP_016873489.1:p.Asp65Ala
XM_017018001.1:c.-337A>C	XP_016873490.1:n.-337A>C
XM_017018002.1:c.-224-1424A>C	XP_016873491.1:n.-224-1424A>C
XM_017018003.2:c.-345A>C	XP_016873492.1:n.-345A>C
XM_017018004.1:c.-345A>C	XP_016873493.1:n.-345A>C
XM_017018005.1:c.-543A>C	XP_016873494.1:n.-543A>C
XM_017018006.2:c.-345A>C	XP_016873495.1:n.-345A>C
NM_017547.4:c.194A>C MANE Select	NP_060017.1:p.Asp65Ala
NR_037647.2:n.139-1424A>C
NR_037648.2:n.371A>C