Canonical Allele Identifier: CA383230231

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145299C>G (hg19) ; chr11:g.126275404C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275404C>G , CM000673.2:g.126275404C>G	GRCh38
NC_000011.9:g.126145299C>G , CM000673.1:g.126145299C>G	GRCh37
NC_000011.8:g.125650509C>G	NCBI36
NG_028029.1:g.11365C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1192C>G
ENST00000532101.6:n.811C>G
ENST00000532125.2:c.706C>G	ENSP00000434178.2:p.Leu236Val
ENST00000533839.6:c.86-390C>G	ENSP00000509952.1:n.86-390C>G
ENST00000534011.6:n.1001C>G
ENST00000685484.1:c.709C>G	ENSP00000510622.1:p.Leu237Val
ENST00000685601.1:c.709C>G	ENSP00000510603.1:p.Leu237Val
ENST00000685765.1:c.709C>G	ENSP00000509991.1:p.Leu237Val
ENST00000685844.1:c.*246C>G	ENSP00000509820.1:n.*246C>G
ENST00000685857.1:n.1448C>G
ENST00000686242.1:c.508C>G	ENSP00000508950.1:n.508C>G
ENST00000686888.1:c.*276C>G	ENSP00000509619.1:n.*276C>G
ENST00000687699.1:c.833C>G	ENSP00000508878.1:n.833C>G
ENST00000687786.1:n.2145C>G
ENST00000688100.1:n.1630C>G
ENST00000688588.1:c.709C>G	ENSP00000510802.1:p.Leu237Val
ENST00000688927.1:n.2920C>G
ENST00000689283.1:c.*372C>G	ENSP00000509050.1:n.*372C>G
ENST00000689477.1:c.*602C>G	ENSP00000508945.1:n.*602C>G
ENST00000689765.1:c.*202C>G	ENSP00000509625.1:n.*202C>G
ENST00000690512.1:c.*560C>G	ENSP00000509793.1:n.*560C>G
ENST00000692039.1:c.*507C>G	ENSP00000508821.1:n.*507C>G
ENST00000692336.1:c.733C>G	ENSP00000508540.1:p.Leu245Val
ENST00000693133.1:n.1189C>G
ENST00000263578.10:c.709C>G MANE Select	ENSP00000263578.5:p.Leu237Val
ENST00000263578.9:c.709C>G	ENSP00000263578.5:p.Leu237Val
ENST00000525083.5:n.429C>G
ENST00000525770.5:c.*341C>G	ENSP00000434739.1:n.*341C>G
ENST00000527004.5:c.*53C>G	ENSP00000436374.1:n.*53C>G
ENST00000530642.1:n.1491C>G
ENST00000532101.5:n.932C>G
ENST00000532125.1:c.667C>G	ENSP00000434178.1:p.Leu223Val
ENST00000533395.5:n.442C>G
ENST00000533839.5:n.238-390C>G
ENST00000534011.5:n.761C>G
ENST00000534315.5:n.1021C>G
NM_017547.3:c.709C>G	NP_060017.1:p.Leu237Val
NR_037647.1:n.655C>G
NR_037648.1:n.895C>G
XM_006718879.2:c.199C>G	XP_006718942.1:p.Leu67Val
XM_006718880.2:c.76C>G	XP_006718943.1:p.Leu26Val
XM_006718881.2:c.76C>G	XP_006718944.1:p.Leu26Val
XM_011542895.1:c.199C>G	XP_011541197.1:p.Leu67Val
XM_011542896.1:c.199C>G	XP_011541198.1:p.Leu67Val
XM_006718879.3:c.199C>G	XP_006718942.1:p.Leu67Val
XM_006718881.3:c.76C>G	XP_006718944.1:p.Leu26Val
XM_011542895.2:c.199C>G	XP_011541197.1:p.Leu67Val
XM_011542896.2:c.199C>G	XP_011541198.1:p.Leu67Val
XM_017018000.2:c.709C>G	XP_016873489.1:p.Leu237Val
XM_017018001.1:c.199C>G	XP_016873490.1:p.Leu67Val
XM_017018002.1:c.199C>G	XP_016873491.1:p.Leu67Val
XM_017018003.2:c.76C>G	XP_016873492.1:p.Leu26Val
XM_017018004.1:c.76C>G	XP_016873493.1:p.Leu26Val
XM_017018005.1:c.76C>G	XP_016873494.1:p.Leu26Val
XM_017018006.2:c.76C>G	XP_016873495.1:p.Leu26Val
NM_017547.4:c.709C>G MANE Select	NP_060017.1:p.Leu237Val
NR_037647.2:n.541C>G
NR_037648.2:n.886C>G