Canonical Allele Identifier: CA383230072

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145224A>G (hg19) ; chr11:g.126275329A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275329A>G , CM000673.2:g.126275329A>G	GRCh38
NC_000011.9:g.126145224A>G , CM000673.1:g.126145224A>G	GRCh37
NC_000011.8:g.125650434A>G	NCBI36
NG_028029.1:g.11290A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1117A>G
ENST00000532101.6:n.736A>G
ENST00000532125.2:c.631A>G	ENSP00000434178.2:p.Met211Val
ENST00000533839.6:c.86-465A>G	ENSP00000509952.1:n.86-465A>G
ENST00000534011.6:n.926A>G
ENST00000685484.1:c.634A>G	ENSP00000510622.1:p.Met212Val
ENST00000685601.1:c.634A>G	ENSP00000510603.1:p.Met212Val
ENST00000685765.1:c.634A>G	ENSP00000509991.1:p.Met212Val
ENST00000685844.1:c.*171A>G	ENSP00000509820.1:n.*171A>G
ENST00000685857.1:n.1373A>G
ENST00000686242.1:c.433A>G	ENSP00000508950.1:n.433A>G
ENST00000686888.1:c.*201A>G	ENSP00000509619.1:n.*201A>G
ENST00000687699.1:c.758A>G	ENSP00000508878.1:n.758A>G
ENST00000687786.1:n.2070A>G
ENST00000688100.1:n.1555A>G
ENST00000688588.1:c.634A>G	ENSP00000510802.1:p.Met212Val
ENST00000688927.1:n.2845A>G
ENST00000689283.1:c.*297A>G	ENSP00000509050.1:n.*297A>G
ENST00000689477.1:c.*527A>G	ENSP00000508945.1:n.*527A>G
ENST00000689765.1:c.*169-42A>G	ENSP00000509625.1:n.*169-42A>G
ENST00000690512.1:c.*485A>G	ENSP00000509793.1:n.*485A>G
ENST00000692039.1:c.*432A>G	ENSP00000508821.1:n.*432A>G
ENST00000692336.1:c.658A>G	ENSP00000508540.1:p.Met220Val
ENST00000693133.1:n.1114A>G
ENST00000263578.10:c.634A>G MANE Select	ENSP00000263578.5:p.Met212Val
ENST00000263578.9:c.634A>G	ENSP00000263578.5:p.Met212Val
ENST00000524751.5:n.875A>G
ENST00000525083.5:n.354A>G
ENST00000525770.5:c.*266A>G	ENSP00000434739.1:n.*266A>G
ENST00000527004.5:c.536A>G	ENSP00000436374.1:p.Asp179Gly
ENST00000530642.1:n.1416A>G
ENST00000532101.5:n.857A>G
ENST00000532125.1:c.592A>G	ENSP00000434178.1:p.Met198Val
ENST00000533395.5:n.367A>G
ENST00000533839.5:n.238-465A>G
ENST00000534011.5:n.686A>G
ENST00000534315.5:n.946A>G
NM_017547.3:c.634A>G	NP_060017.1:p.Met212Val
NR_037647.1:n.580A>G
NR_037648.1:n.820A>G
XM_006718879.2:c.124A>G	XP_006718942.1:p.Met42Val
XM_006718880.2:c.1A>G	XP_006718943.1:p.Met1Val
XM_006718881.2:c.1A>G	XP_006718944.1:p.Met1Val
XM_011542895.1:c.124A>G	XP_011541197.1:p.Met42Val
XM_011542896.1:c.124A>G	XP_011541198.1:p.Met42Val
XM_006718879.3:c.124A>G	XP_006718942.1:p.Met42Val
XM_006718881.3:c.1A>G	XP_006718944.1:p.Met1Val
XM_011542895.2:c.124A>G	XP_011541197.1:p.Met42Val
XM_011542896.2:c.124A>G	XP_011541198.1:p.Met42Val
XM_017018000.2:c.634A>G	XP_016873489.1:p.Met212Val
XM_017018001.1:c.124A>G	XP_016873490.1:p.Met42Val
XM_017018002.1:c.124A>G	XP_016873491.1:p.Met42Val
XM_017018003.2:c.1A>G	XP_016873492.1:p.Met1Val
XM_017018004.1:c.1A>G	XP_016873493.1:p.Met1Val
XM_017018005.1:c.1A>G	XP_016873494.1:p.Met1Val
XM_017018006.2:c.1A>G	XP_016873495.1:p.Met1Val
NM_017547.4:c.634A>G MANE Select	NP_060017.1:p.Met212Val
NR_037647.2:n.466A>G
NR_037648.2:n.811A>G