Canonical Allele Identifier: CA477516002

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145247C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275352C>T , CM000673.2:g.126275352C>T	GRCh38
NC_000011.9:g.126145247C>T , CM000673.1:g.126145247C>T	GRCh37
NC_000011.8:g.125650457C>T	NCBI36
NG_028029.1:g.11313C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1140C>T
ENST00000532101.6:n.759C>T
ENST00000532125.2:c.654C>T	ENSP00000434178.2:p.Asp218=
ENST00000533839.6:c.86-442C>T	ENSP00000509952.1:n.86-442C>T
ENST00000534011.6:n.949C>T
ENST00000685484.1:c.657C>T	ENSP00000510622.1:p.Asp219=
ENST00000685601.1:c.657C>T	ENSP00000510603.1:p.Asp219=
ENST00000685765.1:c.657C>T	ENSP00000509991.1:p.Asp219=
ENST00000685844.1:c.*194C>T	ENSP00000509820.1:n.*194C>T
ENST00000685857.1:n.1396C>T
ENST00000686242.1:c.456C>T	ENSP00000508950.1:n.456C>T
ENST00000686888.1:c.*224C>T	ENSP00000509619.1:n.*224C>T
ENST00000687699.1:c.781C>T	ENSP00000508878.1:n.781C>T
ENST00000687786.1:n.2093C>T
ENST00000688100.1:n.1578C>T
ENST00000688588.1:c.657C>T	ENSP00000510802.1:p.Asp219=
ENST00000688927.1:n.2868C>T
ENST00000689283.1:c.*320C>T	ENSP00000509050.1:n.*320C>T
ENST00000689477.1:c.*550C>T	ENSP00000508945.1:n.*550C>T
ENST00000689765.1:c.*169-19C>T	ENSP00000509625.1:n.*169-19C>T
ENST00000690512.1:c.*508C>T	ENSP00000509793.1:n.*508C>T
ENST00000692039.1:c.*455C>T	ENSP00000508821.1:n.*455C>T
ENST00000692336.1:c.681C>T	ENSP00000508540.1:p.Asp227=
ENST00000693133.1:n.1137C>T
ENST00000263578.10:c.657C>T MANE Select	ENSP00000263578.5:p.Asp219=
ENST00000263578.9:c.657C>T	ENSP00000263578.5:p.Asp219=
ENST00000525083.5:n.377C>T
ENST00000525770.5:c.*289C>T	ENSP00000434739.1:n.*289C>T
ENST00000527004.5:c.*1C>T	ENSP00000436374.1:n.*1C>T
ENST00000530642.1:n.1439C>T
ENST00000532101.5:n.880C>T
ENST00000532125.1:c.615C>T	ENSP00000434178.1:p.Asp205=
ENST00000533395.5:n.390C>T
ENST00000533839.5:n.238-442C>T
ENST00000534011.5:n.709C>T
ENST00000534315.5:n.969C>T
NM_017547.3:c.657C>T	NP_060017.1:p.Asp219=
NR_037647.1:n.603C>T
NR_037648.1:n.843C>T
XM_006718879.2:c.147C>T	XP_006718942.1:p.Asp49=
XM_006718880.2:c.24C>T	XP_006718943.1:p.Asp8=
XM_006718881.2:c.24C>T	XP_006718944.1:p.Asp8=
XM_011542895.1:c.147C>T	XP_011541197.1:p.Asp49=
XM_011542896.1:c.147C>T	XP_011541198.1:p.Asp49=
XM_006718879.3:c.147C>T	XP_006718942.1:p.Asp49=
XM_006718881.3:c.24C>T	XP_006718944.1:p.Asp8=
XM_011542895.2:c.147C>T	XP_011541197.1:p.Asp49=
XM_011542896.2:c.147C>T	XP_011541198.1:p.Asp49=
XM_017018000.2:c.657C>T	XP_016873489.1:p.Asp219=
XM_017018001.1:c.147C>T	XP_016873490.1:p.Asp49=
XM_017018002.1:c.147C>T	XP_016873491.1:p.Asp49=
XM_017018003.2:c.24C>T	XP_016873492.1:p.Asp8=
XM_017018004.1:c.24C>T	XP_016873493.1:p.Asp8=
XM_017018005.1:c.24C>T	XP_016873494.1:p.Asp8=
XM_017018006.2:c.24C>T	XP_016873495.1:p.Asp8=
NM_017547.4:c.657C>T MANE Select	NP_060017.1:p.Asp219=
NR_037647.2:n.489C>T
NR_037648.2:n.834C>T