Canonical Allele Identifier: CA477516102

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145298C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275403C>G , CM000673.2:g.126275403C>G	GRCh38
NC_000011.9:g.126145298C>G , CM000673.1:g.126145298C>G	GRCh37
NC_000011.8:g.125650508C>G	NCBI36
NG_028029.1:g.11364C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1191C>G
ENST00000532101.6:n.810C>G
ENST00000532125.2:c.705C>G	ENSP00000434178.2:p.Val235=
ENST00000533839.6:c.86-391C>G	ENSP00000509952.1:n.86-391C>G
ENST00000534011.6:n.1000C>G
ENST00000685484.1:c.708C>G	ENSP00000510622.1:p.Val236=
ENST00000685601.1:c.708C>G	ENSP00000510603.1:p.Val236=
ENST00000685765.1:c.708C>G	ENSP00000509991.1:p.Val236=
ENST00000685844.1:c.*245C>G	ENSP00000509820.1:n.*245C>G
ENST00000685857.1:n.1447C>G
ENST00000686242.1:c.507C>G	ENSP00000508950.1:n.507C>G
ENST00000686888.1:c.*275C>G	ENSP00000509619.1:n.*275C>G
ENST00000687699.1:c.832C>G	ENSP00000508878.1:n.832C>G
ENST00000687786.1:n.2144C>G
ENST00000688100.1:n.1629C>G
ENST00000688588.1:c.708C>G	ENSP00000510802.1:p.Val236=
ENST00000688927.1:n.2919C>G
ENST00000689283.1:c.*371C>G	ENSP00000509050.1:n.*371C>G
ENST00000689477.1:c.*601C>G	ENSP00000508945.1:n.*601C>G
ENST00000689765.1:c.*201C>G	ENSP00000509625.1:n.*201C>G
ENST00000690512.1:c.*559C>G	ENSP00000509793.1:n.*559C>G
ENST00000692039.1:c.*506C>G	ENSP00000508821.1:n.*506C>G
ENST00000692336.1:c.732C>G	ENSP00000508540.1:p.Val244=
ENST00000693133.1:n.1188C>G
ENST00000263578.10:c.708C>G MANE Select	ENSP00000263578.5:p.Val236=
ENST00000263578.9:c.708C>G	ENSP00000263578.5:p.Val236=
ENST00000525083.5:n.428C>G
ENST00000525770.5:c.*340C>G	ENSP00000434739.1:n.*340C>G
ENST00000527004.5:c.*52C>G	ENSP00000436374.1:n.*52C>G
ENST00000530642.1:n.1490C>G
ENST00000532101.5:n.931C>G
ENST00000532125.1:c.666C>G	ENSP00000434178.1:p.Val222=
ENST00000533395.5:n.441C>G
ENST00000533839.5:n.238-391C>G
ENST00000534011.5:n.760C>G
ENST00000534315.5:n.1020C>G
NM_017547.3:c.708C>G	NP_060017.1:p.Val236=
NR_037647.1:n.654C>G
NR_037648.1:n.894C>G
XM_006718879.2:c.198C>G	XP_006718942.1:p.Val66=
XM_006718880.2:c.75C>G	XP_006718943.1:p.Val25=
XM_006718881.2:c.75C>G	XP_006718944.1:p.Val25=
XM_011542895.1:c.198C>G	XP_011541197.1:p.Val66=
XM_011542896.1:c.198C>G	XP_011541198.1:p.Val66=
XM_006718879.3:c.198C>G	XP_006718942.1:p.Val66=
XM_006718881.3:c.75C>G	XP_006718944.1:p.Val25=
XM_011542895.2:c.198C>G	XP_011541197.1:p.Val66=
XM_011542896.2:c.198C>G	XP_011541198.1:p.Val66=
XM_017018000.2:c.708C>G	XP_016873489.1:p.Val236=
XM_017018001.1:c.198C>G	XP_016873490.1:p.Val66=
XM_017018002.1:c.198C>G	XP_016873491.1:p.Val66=
XM_017018003.2:c.75C>G	XP_016873492.1:p.Val25=
XM_017018004.1:c.75C>G	XP_016873493.1:p.Val25=
XM_017018005.1:c.75C>G	XP_016873494.1:p.Val25=
XM_017018006.2:c.75C>G	XP_016873495.1:p.Val25=
NM_017547.4:c.708C>G MANE Select	NP_060017.1:p.Val236=
NR_037647.2:n.540C>G
NR_037648.2:n.885C>G