Canonical Allele Identifier: CA477513393

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126141384T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126271489T>A , CM000673.2:g.126271489T>A	GRCh38
NC_000011.9:g.126141384T>A , CM000673.1:g.126141384T>A	GRCh37
NC_000011.8:g.125646594T>A	NCBI36
NG_028029.1:g.7450T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.316T>A
ENST00000532101.6:n.315T>A
ENST00000532125.2:c.138T>A	ENSP00000434178.2:p.Pro46=
ENST00000533839.6:c.85+2198T>A	ENSP00000509952.1:n.85+2198T>A
ENST00000534011.6:n.414T>A
ENST00000685484.1:c.138T>A	ENSP00000510622.1:p.Pro46=
ENST00000685601.1:c.138T>A	ENSP00000510603.1:p.Pro46=
ENST00000685765.1:c.138T>A	ENSP00000509991.1:p.Pro46=
ENST00000685844.1:c.86-1480T>A	ENSP00000509820.1:n.86-1480T>A
ENST00000685857.1:n.316T>A
ENST00000686242.1:c.86-1480T>A	ENSP00000508950.1:n.86-1480T>A
ENST00000686888.1:c.138T>A	ENSP00000509619.1:p.Pro46=
ENST00000687699.1:c.262T>A	ENSP00000508878.1:n.262T>A
ENST00000687786.1:n.1471T>A
ENST00000688588.1:c.138T>A	ENSP00000510802.1:p.Pro46=
ENST00000688927.1:n.316T>A
ENST00000689283.1:c.210-1480T>A	ENSP00000509050.1:n.210-1480T>A
ENST00000689477.1:c.*31T>A	ENSP00000508945.1:n.*31T>A
ENST00000689765.1:c.86-1480T>A	ENSP00000509625.1:n.86-1480T>A
ENST00000690512.1:c.86-989T>A	ENSP00000509793.1:n.86-989T>A
ENST00000692039.1:c.224T>A	ENSP00000508821.1:p.Leu75Gln
ENST00000692336.1:c.138T>A	ENSP00000508540.1:p.Pro46=
ENST00000693133.1:n.226-1480T>A
ENST00000263578.10:c.138T>A MANE Select	ENSP00000263578.5:p.Pro46=
ENST00000263578.9:c.138T>A	ENSP00000263578.5:p.Pro46=
ENST00000524751.5:n.223-1480T>A
ENST00000525083.5:n.122-1480T>A
ENST00000525770.5:c.86-1480T>A	ENSP00000434739.1:n.86-1480T>A
ENST00000526366.5:n.101-230T>A
ENST00000526525.1:n.246-1480T>A
ENST00000527004.5:c.138T>A	ENSP00000436374.1:p.Pro46=
ENST00000529802.1:n.188T>A
ENST00000532101.5:n.361T>A
ENST00000532125.1:c.96T>A	ENSP00000434178.1:p.Pro32=
ENST00000533839.5:n.237+2198T>A
ENST00000534011.5:n.158-989T>A
ENST00000534315.5:n.545T>A
NM_017547.3:c.138T>A	NP_060017.1:p.Pro46=
NR_037647.1:n.253-1480T>A
NR_037648.1:n.324T>A
XM_006718880.2:c.-401T>A	XP_006718943.1:n.-401T>A
XM_006718881.2:c.-232-1480T>A	XP_006718944.1:n.-232-1480T>A
XM_011542895.1:c.-373T>A	XP_011541197.1:n.-373T>A
XM_011542896.1:c.-393T>A	XP_011541198.1:n.-393T>A
XM_006718881.3:c.-232-1480T>A	XP_006718944.1:n.-232-1480T>A
XM_011542895.2:c.-373T>A	XP_011541197.1:n.-373T>A
XM_011542896.2:c.-393T>A	XP_011541198.1:n.-393T>A
XM_017018000.2:c.138T>A	XP_016873489.1:p.Pro46=
XM_017018001.1:c.-393T>A	XP_016873490.1:n.-393T>A
XM_017018002.1:c.-224-1480T>A	XP_016873491.1:n.-224-1480T>A
XM_017018003.2:c.-401T>A	XP_016873492.1:n.-401T>A
XM_017018004.1:c.-401T>A	XP_016873493.1:n.-401T>A
XM_017018005.1:c.-599T>A	XP_016873494.1:n.-599T>A
XM_017018006.2:c.-401T>A	XP_016873495.1:n.-401T>A
NM_017547.4:c.138T>A MANE Select	NP_060017.1:p.Pro46=
NR_037647.2:n.139-1480T>A
NR_037648.2:n.315T>A