Canonical Allele Identifier: CA383229999

Gene: FOXRED1

Linked Data

• gnomAD v4: 11-126274994-A-G
• MyVariant Identifiers: chr11:g.126144889A>G (hg19) ; chr11:g.126274994A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274994A>G , CM000673.2:g.126274994A>G	GRCh38
NC_000011.9:g.126144889A>G , CM000673.1:g.126144889A>G	GRCh37
NC_000011.8:g.125650099A>G	NCBI36
NG_028029.1:g.10955A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.782A>G
ENST00000532101.6:n.734-333A>G
ENST00000532125.2:c.601A>G	ENSP00000434178.2:p.Thr201Ala
ENST00000533839.6:c.86-800A>G	ENSP00000509952.1:n.86-800A>G
ENST00000534011.6:n.896A>G
ENST00000685484.1:c.604A>G	ENSP00000510622.1:p.Thr202Ala
ENST00000685601.1:c.604A>G	ENSP00000510603.1:p.Thr202Ala
ENST00000685765.1:c.604A>G	ENSP00000509991.1:p.Thr202Ala
ENST00000685844.1:c.*169-333A>G	ENSP00000509820.1:n.*169-333A>G
ENST00000685857.1:n.1038A>G
ENST00000686242.1:c.403A>G	ENSP00000508950.1:n.403A>G
ENST00000686888.1:c.*171A>G	ENSP00000509619.1:n.*171A>G
ENST00000687699.1:c.728A>G	ENSP00000508878.1:n.728A>G
ENST00000687786.1:n.2068-333A>G
ENST00000688100.1:n.1525A>G
ENST00000688588.1:c.604A>G	ENSP00000510802.1:p.Thr202Ala
ENST00000688927.1:n.2510A>G
ENST00000689283.1:c.*267A>G	ENSP00000509050.1:n.*267A>G
ENST00000689477.1:c.*497A>G	ENSP00000508945.1:n.*497A>G
ENST00000689765.1:c.*169-377A>G	ENSP00000509625.1:n.*169-377A>G
ENST00000690512.1:c.*455A>G	ENSP00000509793.1:n.*455A>G
ENST00000692039.1:c.*402A>G	ENSP00000508821.1:n.*402A>G
ENST00000692336.1:c.628A>G	ENSP00000508540.1:p.Thr210Ala
ENST00000693133.1:n.779A>G
ENST00000263578.10:c.604A>G MANE Select	ENSP00000263578.5:p.Thr202Ala
ENST00000263578.9:c.604A>G	ENSP00000263578.5:p.Thr202Ala
ENST00000524751.5:n.540A>G
ENST00000525083.5:n.352-333A>G
ENST00000525770.5:c.*236A>G	ENSP00000434739.1:n.*236A>G
ENST00000526366.5:n.535A>G
ENST00000527004.5:c.534-333A>G	ENSP00000436374.1:n.534-333A>G
ENST00000527875.1:n.434A>G
ENST00000530642.1:n.1081A>G
ENST00000532101.5:n.827A>G
ENST00000532125.1:c.562A>G	ENSP00000434178.1:p.Thr188Ala
ENST00000533395.5:n.365-333A>G
ENST00000533839.5:n.238-800A>G
ENST00000534011.5:n.656A>G
ENST00000534315.5:n.944-333A>G
NM_017547.3:c.604A>G	NP_060017.1:p.Thr202Ala
NR_037647.1:n.550A>G
NR_037648.1:n.790A>G
XM_006718879.2:c.94A>G	XP_006718942.1:p.Thr32Ala
XM_006718880.2:c.-2-333A>G	XP_006718943.1:n.-2-333A>G
XM_006718881.2:c.-2-333A>G	XP_006718944.1:n.-2-333A>G
XM_011542895.1:c.94A>G	XP_011541197.1:p.Thr32Ala
XM_011542896.1:c.94A>G	XP_011541198.1:p.Thr32Ala
XM_006718879.3:c.94A>G	XP_006718942.1:p.Thr32Ala
XM_006718881.3:c.-2-333A>G	XP_006718944.1:n.-2-333A>G
XM_011542895.2:c.94A>G	XP_011541197.1:p.Thr32Ala
XM_011542896.2:c.94A>G	XP_011541198.1:p.Thr32Ala
XM_017018000.2:c.604A>G	XP_016873489.1:p.Thr202Ala
XM_017018001.1:c.94A>G	XP_016873490.1:p.Thr32Ala
XM_017018002.1:c.94A>G	XP_016873491.1:p.Thr32Ala
XM_017018003.2:c.-2-333A>G	XP_016873492.1:n.-2-333A>G
XM_017018004.1:c.-2-333A>G	XP_016873493.1:n.-2-333A>G
XM_017018005.1:c.-2-333A>G	XP_016873494.1:n.-2-333A>G
XM_017018006.2:c.-2-333A>G	XP_016873495.1:n.-2-333A>G
NM_017547.4:c.604A>G MANE Select	NP_060017.1:p.Thr202Ala
NR_037647.2:n.436A>G
NR_037648.2:n.781A>G