Canonical Allele Identifier: CA383230148

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145255G>C (hg19) ; chr11:g.126275360G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275360G>C , CM000673.2:g.126275360G>C	GRCh38
NC_000011.9:g.126145255G>C , CM000673.1:g.126145255G>C	GRCh37
NC_000011.8:g.125650465G>C	NCBI36
NG_028029.1:g.11321G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1148G>C
ENST00000532101.6:n.767G>C
ENST00000532125.2:c.662G>C	ENSP00000434178.2:p.Cys221Ser
ENST00000533839.6:c.86-434G>C	ENSP00000509952.1:n.86-434G>C
ENST00000534011.6:n.957G>C
ENST00000685484.1:c.665G>C	ENSP00000510622.1:p.Cys222Ser
ENST00000685601.1:c.665G>C	ENSP00000510603.1:p.Cys222Ser
ENST00000685765.1:c.665G>C	ENSP00000509991.1:p.Cys222Ser
ENST00000685844.1:c.*202G>C	ENSP00000509820.1:n.*202G>C
ENST00000685857.1:n.1404G>C
ENST00000686242.1:c.464G>C	ENSP00000508950.1:n.464G>C
ENST00000686888.1:c.*232G>C	ENSP00000509619.1:n.*232G>C
ENST00000687699.1:c.789G>C	ENSP00000508878.1:n.789G>C
ENST00000687786.1:n.2101G>C
ENST00000688100.1:n.1586G>C
ENST00000688588.1:c.665G>C	ENSP00000510802.1:p.Cys222Ser
ENST00000688927.1:n.2876G>C
ENST00000689283.1:c.*328G>C	ENSP00000509050.1:n.*328G>C
ENST00000689477.1:c.*558G>C	ENSP00000508945.1:n.*558G>C
ENST00000689765.1:c.*169-11G>C	ENSP00000509625.1:n.*169-11G>C
ENST00000690512.1:c.*516G>C	ENSP00000509793.1:n.*516G>C
ENST00000692039.1:c.*463G>C	ENSP00000508821.1:n.*463G>C
ENST00000692336.1:c.689G>C	ENSP00000508540.1:p.Cys230Ser
ENST00000693133.1:n.1145G>C
ENST00000263578.10:c.665G>C MANE Select	ENSP00000263578.5:p.Cys222Ser
ENST00000263578.9:c.665G>C	ENSP00000263578.5:p.Cys222Ser
ENST00000525083.5:n.385G>C
ENST00000525770.5:c.*297G>C	ENSP00000434739.1:n.*297G>C
ENST00000527004.5:c.*9G>C	ENSP00000436374.1:n.*9G>C
ENST00000530642.1:n.1447G>C
ENST00000532101.5:n.888G>C
ENST00000532125.1:c.623G>C	ENSP00000434178.1:p.Cys208Ser
ENST00000533395.5:n.398G>C
ENST00000533839.5:n.238-434G>C
ENST00000534011.5:n.717G>C
ENST00000534315.5:n.977G>C
NM_017547.3:c.665G>C	NP_060017.1:p.Cys222Ser
NR_037647.1:n.611G>C
NR_037648.1:n.851G>C
XM_006718879.2:c.155G>C	XP_006718942.1:p.Cys52Ser
XM_006718880.2:c.32G>C	XP_006718943.1:p.Cys11Ser
XM_006718881.2:c.32G>C	XP_006718944.1:p.Cys11Ser
XM_011542895.1:c.155G>C	XP_011541197.1:p.Cys52Ser
XM_011542896.1:c.155G>C	XP_011541198.1:p.Cys52Ser
XM_006718879.3:c.155G>C	XP_006718942.1:p.Cys52Ser
XM_006718881.3:c.32G>C	XP_006718944.1:p.Cys11Ser
XM_011542895.2:c.155G>C	XP_011541197.1:p.Cys52Ser
XM_011542896.2:c.155G>C	XP_011541198.1:p.Cys52Ser
XM_017018000.2:c.665G>C	XP_016873489.1:p.Cys222Ser
XM_017018001.1:c.155G>C	XP_016873490.1:p.Cys52Ser
XM_017018002.1:c.155G>C	XP_016873491.1:p.Cys52Ser
XM_017018003.2:c.32G>C	XP_016873492.1:p.Cys11Ser
XM_017018004.1:c.32G>C	XP_016873493.1:p.Cys11Ser
XM_017018005.1:c.32G>C	XP_016873494.1:p.Cys11Ser
XM_017018006.2:c.32G>C	XP_016873495.1:p.Cys11Ser
NM_017547.4:c.665G>C MANE Select	NP_060017.1:p.Cys222Ser
NR_037647.2:n.497G>C
NR_037648.2:n.842G>C