Canonical Allele Identifier: CA477516078

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145271T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275376T>C , CM000673.2:g.126275376T>C	GRCh38
NC_000011.9:g.126145271T>C , CM000673.1:g.126145271T>C	GRCh37
NC_000011.8:g.125650481T>C	NCBI36
NG_028029.1:g.11337T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1164T>C
ENST00000532101.6:n.783T>C
ENST00000532125.2:c.678T>C	ENSP00000434178.2:p.Leu226=
ENST00000533839.6:c.86-418T>C	ENSP00000509952.1:n.86-418T>C
ENST00000534011.6:n.973T>C
ENST00000685484.1:c.681T>C	ENSP00000510622.1:p.Leu227=
ENST00000685601.1:c.681T>C	ENSP00000510603.1:p.Leu227=
ENST00000685765.1:c.681T>C	ENSP00000509991.1:p.Leu227=
ENST00000685844.1:c.*218T>C	ENSP00000509820.1:n.*218T>C
ENST00000685857.1:n.1420T>C
ENST00000686242.1:c.480T>C	ENSP00000508950.1:n.480T>C
ENST00000686888.1:c.*248T>C	ENSP00000509619.1:n.*248T>C
ENST00000687699.1:c.805T>C	ENSP00000508878.1:n.805T>C
ENST00000687786.1:n.2117T>C
ENST00000688100.1:n.1602T>C
ENST00000688588.1:c.681T>C	ENSP00000510802.1:p.Leu227=
ENST00000688927.1:n.2892T>C
ENST00000689283.1:c.*344T>C	ENSP00000509050.1:n.*344T>C
ENST00000689477.1:c.*574T>C	ENSP00000508945.1:n.*574T>C
ENST00000689765.1:c.*174T>C	ENSP00000509625.1:n.*174T>C
ENST00000690512.1:c.*532T>C	ENSP00000509793.1:n.*532T>C
ENST00000692039.1:c.*479T>C	ENSP00000508821.1:n.*479T>C
ENST00000692336.1:c.705T>C	ENSP00000508540.1:p.Leu235=
ENST00000693133.1:n.1161T>C
ENST00000263578.10:c.681T>C MANE Select	ENSP00000263578.5:p.Leu227=
ENST00000263578.9:c.681T>C	ENSP00000263578.5:p.Leu227=
ENST00000525083.5:n.401T>C
ENST00000525770.5:c.*313T>C	ENSP00000434739.1:n.*313T>C
ENST00000527004.5:c.*25T>C	ENSP00000436374.1:n.*25T>C
ENST00000530642.1:n.1463T>C
ENST00000532101.5:n.904T>C
ENST00000532125.1:c.639T>C	ENSP00000434178.1:p.Leu213=
ENST00000533395.5:n.414T>C
ENST00000533839.5:n.238-418T>C
ENST00000534011.5:n.733T>C
ENST00000534315.5:n.993T>C
NM_017547.3:c.681T>C	NP_060017.1:p.Leu227=
NR_037647.1:n.627T>C
NR_037648.1:n.867T>C
XM_006718879.2:c.171T>C	XP_006718942.1:p.Leu57=
XM_006718880.2:c.48T>C	XP_006718943.1:p.Leu16=
XM_006718881.2:c.48T>C	XP_006718944.1:p.Leu16=
XM_011542895.1:c.171T>C	XP_011541197.1:p.Leu57=
XM_011542896.1:c.171T>C	XP_011541198.1:p.Leu57=
XM_006718879.3:c.171T>C	XP_006718942.1:p.Leu57=
XM_006718881.3:c.48T>C	XP_006718944.1:p.Leu16=
XM_011542895.2:c.171T>C	XP_011541197.1:p.Leu57=
XM_011542896.2:c.171T>C	XP_011541198.1:p.Leu57=
XM_017018000.2:c.681T>C	XP_016873489.1:p.Leu227=
XM_017018001.1:c.171T>C	XP_016873490.1:p.Leu57=
XM_017018002.1:c.171T>C	XP_016873491.1:p.Leu57=
XM_017018003.2:c.48T>C	XP_016873492.1:p.Leu16=
XM_017018004.1:c.48T>C	XP_016873493.1:p.Leu16=
XM_017018005.1:c.48T>C	XP_016873494.1:p.Leu16=
XM_017018006.2:c.48T>C	XP_016873495.1:p.Leu16=
NM_017547.4:c.681T>C MANE Select	NP_060017.1:p.Leu227=
NR_037647.2:n.513T>C
NR_037648.2:n.858T>C