Canonical Allele Identifier: CA383230092

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145231A>G (hg19) ; chr11:g.126275336A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275336A>G , CM000673.2:g.126275336A>G	GRCh38
NC_000011.9:g.126145231A>G , CM000673.1:g.126145231A>G	GRCh37
NC_000011.8:g.125650441A>G	NCBI36
NG_028029.1:g.11297A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1124A>G
ENST00000532101.6:n.743A>G
ENST00000532125.2:c.638A>G	ENSP00000434178.2:p.Asp213Gly
ENST00000533839.6:c.86-458A>G	ENSP00000509952.1:n.86-458A>G
ENST00000534011.6:n.933A>G
ENST00000685484.1:c.641A>G	ENSP00000510622.1:p.Asp214Gly
ENST00000685601.1:c.641A>G	ENSP00000510603.1:p.Asp214Gly
ENST00000685765.1:c.641A>G	ENSP00000509991.1:p.Asp214Gly
ENST00000685844.1:c.*178A>G	ENSP00000509820.1:n.*178A>G
ENST00000685857.1:n.1380A>G
ENST00000686242.1:c.440A>G	ENSP00000508950.1:n.440A>G
ENST00000686888.1:c.*208A>G	ENSP00000509619.1:n.*208A>G
ENST00000687699.1:c.765A>G	ENSP00000508878.1:n.765A>G
ENST00000687786.1:n.2077A>G
ENST00000688100.1:n.1562A>G
ENST00000688588.1:c.641A>G	ENSP00000510802.1:p.Asp214Gly
ENST00000688927.1:n.2852A>G
ENST00000689283.1:c.*304A>G	ENSP00000509050.1:n.*304A>G
ENST00000689477.1:c.*534A>G	ENSP00000508945.1:n.*534A>G
ENST00000689765.1:c.*169-35A>G	ENSP00000509625.1:n.*169-35A>G
ENST00000690512.1:c.*492A>G	ENSP00000509793.1:n.*492A>G
ENST00000692039.1:c.*439A>G	ENSP00000508821.1:n.*439A>G
ENST00000692336.1:c.665A>G	ENSP00000508540.1:p.Asp222Gly
ENST00000693133.1:n.1121A>G
ENST00000263578.10:c.641A>G MANE Select	ENSP00000263578.5:p.Asp214Gly
ENST00000263578.9:c.641A>G	ENSP00000263578.5:p.Asp214Gly
ENST00000524751.5:n.882A>G
ENST00000525083.5:n.361A>G
ENST00000525770.5:c.*273A>G	ENSP00000434739.1:n.*273A>G
ENST00000527004.5:c.543A>G	ENSP00000436374.1:p.Gly181=
ENST00000530642.1:n.1423A>G
ENST00000532101.5:n.864A>G
ENST00000532125.1:c.599A>G	ENSP00000434178.1:p.Asp200Gly
ENST00000533395.5:n.374A>G
ENST00000533839.5:n.238-458A>G
ENST00000534011.5:n.693A>G
ENST00000534315.5:n.953A>G
NM_017547.3:c.641A>G	NP_060017.1:p.Asp214Gly
NR_037647.1:n.587A>G
NR_037648.1:n.827A>G
XM_006718879.2:c.131A>G	XP_006718942.1:p.Asp44Gly
XM_006718880.2:c.8A>G	XP_006718943.1:p.Asp3Gly
XM_006718881.2:c.8A>G	XP_006718944.1:p.Asp3Gly
XM_011542895.1:c.131A>G	XP_011541197.1:p.Asp44Gly
XM_011542896.1:c.131A>G	XP_011541198.1:p.Asp44Gly
XM_006718879.3:c.131A>G	XP_006718942.1:p.Asp44Gly
XM_006718881.3:c.8A>G	XP_006718944.1:p.Asp3Gly
XM_011542895.2:c.131A>G	XP_011541197.1:p.Asp44Gly
XM_011542896.2:c.131A>G	XP_011541198.1:p.Asp44Gly
XM_017018000.2:c.641A>G	XP_016873489.1:p.Asp214Gly
XM_017018001.1:c.131A>G	XP_016873490.1:p.Asp44Gly
XM_017018002.1:c.131A>G	XP_016873491.1:p.Asp44Gly
XM_017018003.2:c.8A>G	XP_016873492.1:p.Asp3Gly
XM_017018004.1:c.8A>G	XP_016873493.1:p.Asp3Gly
XM_017018005.1:c.8A>G	XP_016873494.1:p.Asp3Gly
XM_017018006.2:c.8A>G	XP_016873495.1:p.Asp3Gly
NM_017547.4:c.641A>G MANE Select	NP_060017.1:p.Asp214Gly
NR_037647.2:n.473A>G
NR_037648.2:n.818A>G