Canonical Allele Identifier: CA383230254

Gene: FOXRED1

Linked Data

• ClinVar Variation Id: 2850062
• ClinVar RCV Id: RCV003688123
• MyVariant Identifiers: chr11:g.126145308C>T (hg19) ; chr11:g.126275413C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275413C>T , CM000673.2:g.126275413C>T	GRCh38
NC_000011.9:g.126145308C>T , CM000673.1:g.126145308C>T	GRCh37
NC_000011.8:g.125650518C>T	NCBI36
NG_028029.1:g.11374C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1201C>T
ENST00000532101.6:n.820C>T
ENST00000532125.2:c.715C>T	ENSP00000434178.2:p.Gln239Ter
ENST00000533839.6:c.86-381C>T	ENSP00000509952.1:n.86-381C>T
ENST00000534011.6:n.1010C>T
ENST00000685484.1:c.718C>T	ENSP00000510622.1:p.Gln240Ter
ENST00000685601.1:c.718C>T	ENSP00000510603.1:p.Gln240Ter
ENST00000685765.1:c.718C>T	ENSP00000509991.1:p.Gln240Ter
ENST00000685844.1:c.*255C>T	ENSP00000509820.1:n.*255C>T
ENST00000685857.1:n.1457C>T
ENST00000686242.1:c.517C>T	ENSP00000508950.1:n.517C>T
ENST00000686888.1:c.*285C>T	ENSP00000509619.1:n.*285C>T
ENST00000687699.1:c.842C>T	ENSP00000508878.1:n.842C>T
ENST00000687786.1:n.2154C>T
ENST00000688100.1:n.1639C>T
ENST00000688588.1:c.718C>T	ENSP00000510802.1:p.Gln240Ter
ENST00000688927.1:n.2929C>T
ENST00000689283.1:c.*381C>T	ENSP00000509050.1:n.*381C>T
ENST00000689477.1:c.*611C>T	ENSP00000508945.1:n.*611C>T
ENST00000689765.1:c.*211C>T	ENSP00000509625.1:n.*211C>T
ENST00000690512.1:c.*569C>T	ENSP00000509793.1:n.*569C>T
ENST00000692039.1:c.*516C>T	ENSP00000508821.1:n.*516C>T
ENST00000692336.1:c.742C>T	ENSP00000508540.1:p.Gln248Ter
ENST00000693133.1:n.1198C>T
ENST00000263578.10:c.718C>T MANE Select	ENSP00000263578.5:p.Gln240Ter
ENST00000263578.9:c.718C>T	ENSP00000263578.5:p.Gln240Ter
ENST00000525083.5:n.438C>T
ENST00000525770.5:c.*350C>T	ENSP00000434739.1:n.*350C>T
ENST00000527004.5:c.*62C>T	ENSP00000436374.1:n.*62C>T
ENST00000530642.1:n.1500C>T
ENST00000532101.5:n.941C>T
ENST00000532125.1:c.676C>T	ENSP00000434178.1:p.Gln226Ter
ENST00000533395.5:n.451C>T
ENST00000533839.5:n.238-381C>T
ENST00000534011.5:n.770C>T
ENST00000534315.5:n.1030C>T
NM_017547.3:c.718C>T	NP_060017.1:p.Gln240Ter
NR_037647.1:n.664C>T
NR_037648.1:n.904C>T
XM_006718879.2:c.208C>T	XP_006718942.1:p.Gln70Ter
XM_006718880.2:c.85C>T	XP_006718943.1:p.Gln29Ter
XM_006718881.2:c.85C>T	XP_006718944.1:p.Gln29Ter
XM_011542895.1:c.208C>T	XP_011541197.1:p.Gln70Ter
XM_011542896.1:c.208C>T	XP_011541198.1:p.Gln70Ter
XM_006718879.3:c.208C>T	XP_006718942.1:p.Gln70Ter
XM_006718881.3:c.85C>T	XP_006718944.1:p.Gln29Ter
XM_011542895.2:c.208C>T	XP_011541197.1:p.Gln70Ter
XM_011542896.2:c.208C>T	XP_011541198.1:p.Gln70Ter
XM_017018000.2:c.718C>T	XP_016873489.1:p.Gln240Ter
XM_017018001.1:c.208C>T	XP_016873490.1:p.Gln70Ter
XM_017018002.1:c.208C>T	XP_016873491.1:p.Gln70Ter
XM_017018003.2:c.85C>T	XP_016873492.1:p.Gln29Ter
XM_017018004.1:c.85C>T	XP_016873493.1:p.Gln29Ter
XM_017018005.1:c.85C>T	XP_016873494.1:p.Gln29Ter
XM_017018006.2:c.85C>T	XP_016873495.1:p.Gln29Ter
NM_017547.4:c.718C>T MANE Select	NP_060017.1:p.Gln240Ter
NR_037647.2:n.550C>T
NR_037648.2:n.895C>T