Canonical Allele Identifier: CA383229189

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126141482C>T (hg19) ; chr11:g.126271587C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126271587C>T , CM000673.2:g.126271587C>T	GRCh38
NC_000011.9:g.126141482C>T , CM000673.1:g.126141482C>T	GRCh37
NC_000011.8:g.125646692C>T	NCBI36
NG_028029.1:g.7548C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.414C>T
ENST00000532101.6:n.413C>T
ENST00000532125.2:c.236C>T	ENSP00000434178.2:p.Ala79Val
ENST00000533839.6:c.85+2296C>T	ENSP00000509952.1:n.85+2296C>T
ENST00000534011.6:n.512C>T
ENST00000685484.1:c.236C>T	ENSP00000510622.1:p.Ala79Val
ENST00000685601.1:c.236C>T	ENSP00000510603.1:p.Ala79Val
ENST00000685765.1:c.236C>T	ENSP00000509991.1:p.Ala79Val
ENST00000685844.1:c.86-1382C>T	ENSP00000509820.1:n.86-1382C>T
ENST00000685857.1:n.414C>T
ENST00000686242.1:c.86-1382C>T	ENSP00000508950.1:n.86-1382C>T
ENST00000686888.1:c.236C>T	ENSP00000509619.1:p.Ala79Val
ENST00000687699.1:c.360C>T	ENSP00000508878.1:n.360C>T
ENST00000687786.1:n.1569C>T
ENST00000688588.1:c.236C>T	ENSP00000510802.1:p.Ala79Val
ENST00000688927.1:n.414C>T
ENST00000689283.1:c.210-1382C>T	ENSP00000509050.1:n.210-1382C>T
ENST00000689477.1:c.*129C>T	ENSP00000508945.1:n.*129C>T
ENST00000689765.1:c.86-1382C>T	ENSP00000509625.1:n.86-1382C>T
ENST00000690512.1:c.86-891C>T	ENSP00000509793.1:n.86-891C>T
ENST00000692039.1:c.*34C>T	ENSP00000508821.1:n.*34C>T
ENST00000692336.1:c.236C>T	ENSP00000508540.1:p.Ala79Val
ENST00000693133.1:n.226-1382C>T
ENST00000263578.10:c.236C>T MANE Select	ENSP00000263578.5:p.Ala79Val
ENST00000263578.9:c.236C>T	ENSP00000263578.5:p.Ala79Val
ENST00000524751.5:n.223-1382C>T
ENST00000525083.5:n.122-1382C>T
ENST00000525770.5:c.86-1382C>T	ENSP00000434739.1:n.86-1382C>T
ENST00000526366.5:n.101-132C>T
ENST00000526525.1:n.246-1382C>T
ENST00000527004.5:c.236C>T	ENSP00000436374.1:p.Ala79Val
ENST00000529802.1:n.286C>T
ENST00000532101.5:n.459C>T
ENST00000532125.1:c.194C>T	ENSP00000434178.1:p.Ala65Val
ENST00000533839.5:n.237+2296C>T
ENST00000534011.5:n.158-891C>T
ENST00000534315.5:n.643C>T
NM_017547.3:c.236C>T	NP_060017.1:p.Ala79Val
NR_037647.1:n.253-1382C>T
NR_037648.1:n.422C>T
XM_006718880.2:c.-303C>T	XP_006718943.1:n.-303C>T
XM_006718881.2:c.-232-1382C>T	XP_006718944.1:n.-232-1382C>T
XM_011542895.1:c.-275C>T	XP_011541197.1:n.-275C>T
XM_011542896.1:c.-295C>T	XP_011541198.1:n.-295C>T
XM_006718881.3:c.-232-1382C>T	XP_006718944.1:n.-232-1382C>T
XM_011542895.2:c.-275C>T	XP_011541197.1:n.-275C>T
XM_011542896.2:c.-295C>T	XP_011541198.1:n.-295C>T
XM_017018000.2:c.236C>T	XP_016873489.1:p.Ala79Val
XM_017018001.1:c.-295C>T	XP_016873490.1:n.-295C>T
XM_017018002.1:c.-224-1382C>T	XP_016873491.1:n.-224-1382C>T
XM_017018003.2:c.-303C>T	XP_016873492.1:n.-303C>T
XM_017018004.1:c.-303C>T	XP_016873493.1:n.-303C>T
XM_017018005.1:c.-501C>T	XP_016873494.1:n.-501C>T
XM_017018006.2:c.-303C>T	XP_016873495.1:n.-303C>T
NM_017547.4:c.236C>T MANE Select	NP_060017.1:p.Ala79Val
NR_037647.2:n.139-1382C>T
NR_037648.2:n.413C>T