Canonical Allele Identifier: CA383229106

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126141439G>A (hg19) ; chr11:g.126271544G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126271544G>A , CM000673.2:g.126271544G>A	GRCh38
NC_000011.9:g.126141439G>A , CM000673.1:g.126141439G>A	GRCh37
NC_000011.8:g.125646649G>A	NCBI36
NG_028029.1:g.7505G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.371G>A
ENST00000532101.6:n.370G>A
ENST00000532125.2:c.193G>A	ENSP00000434178.2:p.Asp65Asn
ENST00000533839.6:c.85+2253G>A	ENSP00000509952.1:n.85+2253G>A
ENST00000534011.6:n.469G>A
ENST00000685484.1:c.193G>A	ENSP00000510622.1:p.Asp65Asn
ENST00000685601.1:c.193G>A	ENSP00000510603.1:p.Asp65Asn
ENST00000685765.1:c.193G>A	ENSP00000509991.1:p.Asp65Asn
ENST00000685844.1:c.86-1425G>A	ENSP00000509820.1:n.86-1425G>A
ENST00000685857.1:n.371G>A
ENST00000686242.1:c.86-1425G>A	ENSP00000508950.1:n.86-1425G>A
ENST00000686888.1:c.193G>A	ENSP00000509619.1:p.Asp65Asn
ENST00000687699.1:c.317G>A	ENSP00000508878.1:n.317G>A
ENST00000687786.1:n.1526G>A
ENST00000688588.1:c.193G>A	ENSP00000510802.1:p.Asp65Asn
ENST00000688927.1:n.371G>A
ENST00000689283.1:c.210-1425G>A	ENSP00000509050.1:n.210-1425G>A
ENST00000689477.1:c.*86G>A	ENSP00000508945.1:n.*86G>A
ENST00000689765.1:c.86-1425G>A	ENSP00000509625.1:n.86-1425G>A
ENST00000690512.1:c.86-934G>A	ENSP00000509793.1:n.86-934G>A
ENST00000692039.1:c.279G>A	ENSP00000508821.1:p.Arg93=
ENST00000692336.1:c.193G>A	ENSP00000508540.1:p.Asp65Asn
ENST00000693133.1:n.226-1425G>A
ENST00000263578.10:c.193G>A MANE Select	ENSP00000263578.5:p.Asp65Asn
ENST00000263578.9:c.193G>A	ENSP00000263578.5:p.Asp65Asn
ENST00000524751.5:n.223-1425G>A
ENST00000525083.5:n.122-1425G>A
ENST00000525770.5:c.86-1425G>A	ENSP00000434739.1:n.86-1425G>A
ENST00000526366.5:n.101-175G>A
ENST00000526525.1:n.246-1425G>A
ENST00000527004.5:c.193G>A	ENSP00000436374.1:p.Asp65Asn
ENST00000529802.1:n.243G>A
ENST00000532101.5:n.416G>A
ENST00000532125.1:c.151G>A	ENSP00000434178.1:p.Asp51Asn
ENST00000533839.5:n.237+2253G>A
ENST00000534011.5:n.158-934G>A
ENST00000534315.5:n.600G>A
NM_017547.3:c.193G>A	NP_060017.1:p.Asp65Asn
NR_037647.1:n.253-1425G>A
NR_037648.1:n.379G>A
XM_006718880.2:c.-346G>A	XP_006718943.1:n.-346G>A
XM_006718881.2:c.-232-1425G>A	XP_006718944.1:n.-232-1425G>A
XM_011542895.1:c.-318G>A	XP_011541197.1:n.-318G>A
XM_011542896.1:c.-338G>A	XP_011541198.1:n.-338G>A
XM_006718881.3:c.-232-1425G>A	XP_006718944.1:n.-232-1425G>A
XM_011542895.2:c.-318G>A	XP_011541197.1:n.-318G>A
XM_011542896.2:c.-338G>A	XP_011541198.1:n.-338G>A
XM_017018000.2:c.193G>A	XP_016873489.1:p.Asp65Asn
XM_017018001.1:c.-338G>A	XP_016873490.1:n.-338G>A
XM_017018002.1:c.-224-1425G>A	XP_016873491.1:n.-224-1425G>A
XM_017018003.2:c.-346G>A	XP_016873492.1:n.-346G>A
XM_017018004.1:c.-346G>A	XP_016873493.1:n.-346G>A
XM_017018005.1:c.-544G>A	XP_016873494.1:n.-544G>A
XM_017018006.2:c.-346G>A	XP_016873495.1:n.-346G>A
NM_017547.4:c.193G>A MANE Select	NP_060017.1:p.Asp65Asn
NR_037647.2:n.139-1425G>A
NR_037648.2:n.370G>A