Canonical Allele Identifier: CA477515989

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145244T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275349T>C , CM000673.2:g.126275349T>C	GRCh38
NC_000011.9:g.126145244T>C , CM000673.1:g.126145244T>C	GRCh37
NC_000011.8:g.125650454T>C	NCBI36
NG_028029.1:g.11310T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1137T>C
ENST00000532101.6:n.756T>C
ENST00000532125.2:c.651T>C	ENSP00000434178.2:p.Phe217=
ENST00000533839.6:c.86-445T>C	ENSP00000509952.1:n.86-445T>C
ENST00000534011.6:n.946T>C
ENST00000685484.1:c.654T>C	ENSP00000510622.1:p.Phe218=
ENST00000685601.1:c.654T>C	ENSP00000510603.1:p.Phe218=
ENST00000685765.1:c.654T>C	ENSP00000509991.1:p.Phe218=
ENST00000685844.1:c.*191T>C	ENSP00000509820.1:n.*191T>C
ENST00000685857.1:n.1393T>C
ENST00000686242.1:c.453T>C	ENSP00000508950.1:n.453T>C
ENST00000686888.1:c.*221T>C	ENSP00000509619.1:n.*221T>C
ENST00000687699.1:c.778T>C	ENSP00000508878.1:n.778T>C
ENST00000687786.1:n.2090T>C
ENST00000688100.1:n.1575T>C
ENST00000688588.1:c.654T>C	ENSP00000510802.1:p.Phe218=
ENST00000688927.1:n.2865T>C
ENST00000689283.1:c.*317T>C	ENSP00000509050.1:n.*317T>C
ENST00000689477.1:c.*547T>C	ENSP00000508945.1:n.*547T>C
ENST00000689765.1:c.*169-22T>C	ENSP00000509625.1:n.*169-22T>C
ENST00000690512.1:c.*505T>C	ENSP00000509793.1:n.*505T>C
ENST00000692039.1:c.*452T>C	ENSP00000508821.1:n.*452T>C
ENST00000692336.1:c.678T>C	ENSP00000508540.1:p.Phe226=
ENST00000693133.1:n.1134T>C
ENST00000263578.10:c.654T>C MANE Select	ENSP00000263578.5:p.Phe218=
ENST00000263578.9:c.654T>C	ENSP00000263578.5:p.Phe218=
ENST00000524751.5:n.895T>C
ENST00000525083.5:n.374T>C
ENST00000525770.5:c.*286T>C	ENSP00000434739.1:n.*286T>C
ENST00000527004.5:c.556T>C	ENSP00000436374.1:p.Ter186Arg
ENST00000530642.1:n.1436T>C
ENST00000532101.5:n.877T>C
ENST00000532125.1:c.612T>C	ENSP00000434178.1:p.Phe204=
ENST00000533395.5:n.387T>C
ENST00000533839.5:n.238-445T>C
ENST00000534011.5:n.706T>C
ENST00000534315.5:n.966T>C
NM_017547.3:c.654T>C	NP_060017.1:p.Phe218=
NR_037647.1:n.600T>C
NR_037648.1:n.840T>C
XM_006718879.2:c.144T>C	XP_006718942.1:p.Phe48=
XM_006718880.2:c.21T>C	XP_006718943.1:p.Phe7=
XM_006718881.2:c.21T>C	XP_006718944.1:p.Phe7=
XM_011542895.1:c.144T>C	XP_011541197.1:p.Phe48=
XM_011542896.1:c.144T>C	XP_011541198.1:p.Phe48=
XM_006718879.3:c.144T>C	XP_006718942.1:p.Phe48=
XM_006718881.3:c.21T>C	XP_006718944.1:p.Phe7=
XM_011542895.2:c.144T>C	XP_011541197.1:p.Phe48=
XM_011542896.2:c.144T>C	XP_011541198.1:p.Phe48=
XM_017018000.2:c.654T>C	XP_016873489.1:p.Phe218=
XM_017018001.1:c.144T>C	XP_016873490.1:p.Phe48=
XM_017018002.1:c.144T>C	XP_016873491.1:p.Phe48=
XM_017018003.2:c.21T>C	XP_016873492.1:p.Phe7=
XM_017018004.1:c.21T>C	XP_016873493.1:p.Phe7=
XM_017018005.1:c.21T>C	XP_016873494.1:p.Phe7=
XM_017018006.2:c.21T>C	XP_016873495.1:p.Phe7=
NM_017547.4:c.654T>C MANE Select	NP_060017.1:p.Phe218=
NR_037647.2:n.486T>C
NR_037648.2:n.831T>C