Canonical Allele Identifier: CA383230221

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145293G>C (hg19) ; chr11:g.126275398G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275398G>C , CM000673.2:g.126275398G>C	GRCh38
NC_000011.9:g.126145293G>C , CM000673.1:g.126145293G>C	GRCh37
NC_000011.8:g.125650503G>C	NCBI36
NG_028029.1:g.11359G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000525083.6:n.1186G>C
ENST00000532101.6:n.805G>C
ENST00000532125.2:c.700G>C	ENSP00000434178.2:p.Gly234Arg
ENST00000533839.6:c.86-396G>C	ENSP00000509952.1:n.86-396G>C
ENST00000534011.6:n.995G>C
ENST00000685484.1:c.703G>C	ENSP00000510622.1:p.Gly235Arg
ENST00000685601.1:c.703G>C	ENSP00000510603.1:p.Gly235Arg
ENST00000685765.1:c.703G>C	ENSP00000509991.1:p.Gly235Arg
ENST00000685844.1:c.*240G>C	ENSP00000509820.1:n.*240G>C
ENST00000685857.1:n.1442G>C
ENST00000686242.1:c.502G>C	ENSP00000508950.1:n.502G>C
ENST00000686888.1:c.*270G>C	ENSP00000509619.1:n.*270G>C
ENST00000687699.1:c.827G>C	ENSP00000508878.1:n.827G>C
ENST00000687786.1:n.2139G>C
ENST00000688100.1:n.1624G>C
ENST00000688588.1:c.703G>C	ENSP00000510802.1:p.Gly235Arg
ENST00000688927.1:n.2914G>C
ENST00000689283.1:c.*366G>C	ENSP00000509050.1:n.*366G>C
ENST00000689477.1:c.*596G>C	ENSP00000508945.1:n.*596G>C
ENST00000689765.1:c.*196G>C	ENSP00000509625.1:n.*196G>C
ENST00000690512.1:c.*554G>C	ENSP00000509793.1:n.*554G>C
ENST00000692039.1:c.*501G>C	ENSP00000508821.1:n.*501G>C
ENST00000692336.1:c.727G>C	ENSP00000508540.1:p.Gly243Arg
ENST00000693133.1:n.1183G>C
ENST00000263578.10:c.703G>C MANE Select	ENSP00000263578.5:p.Gly235Arg
ENST00000263578.9:c.703G>C	ENSP00000263578.5:p.Gly235Arg
ENST00000525083.5:n.423G>C
ENST00000525770.5:c.*335G>C	ENSP00000434739.1:n.*335G>C
ENST00000527004.5:c.*47G>C	ENSP00000436374.1:n.*47G>C
ENST00000530642.1:n.1485G>C
ENST00000532101.5:n.926G>C
ENST00000532125.1:c.661G>C	ENSP00000434178.1:p.Gly221Arg
ENST00000533395.5:n.436G>C
ENST00000533839.5:n.238-396G>C
ENST00000534011.5:n.755G>C
ENST00000534315.5:n.1015G>C
NM_017547.3:c.703G>C	NP_060017.1:p.Gly235Arg
NR_037647.1:n.649G>C
NR_037648.1:n.889G>C
XM_006718879.2:c.193G>C	XP_006718942.1:p.Gly65Arg
XM_006718880.2:c.70G>C	XP_006718943.1:p.Gly24Arg
XM_006718881.2:c.70G>C	XP_006718944.1:p.Gly24Arg
XM_011542895.1:c.193G>C	XP_011541197.1:p.Gly65Arg
XM_011542896.1:c.193G>C	XP_011541198.1:p.Gly65Arg
XM_006718879.3:c.193G>C	XP_006718942.1:p.Gly65Arg
XM_006718881.3:c.70G>C	XP_006718944.1:p.Gly24Arg
XM_011542895.2:c.193G>C	XP_011541197.1:p.Gly65Arg
XM_011542896.2:c.193G>C	XP_011541198.1:p.Gly65Arg
XM_017018000.2:c.703G>C	XP_016873489.1:p.Gly235Arg
XM_017018001.1:c.193G>C	XP_016873490.1:p.Gly65Arg
XM_017018002.1:c.193G>C	XP_016873491.1:p.Gly65Arg
XM_017018003.2:c.70G>C	XP_016873492.1:p.Gly24Arg
XM_017018004.1:c.70G>C	XP_016873493.1:p.Gly24Arg
XM_017018005.1:c.70G>C	XP_016873494.1:p.Gly24Arg
XM_017018006.2:c.70G>C	XP_016873495.1:p.Gly24Arg
NM_017547.4:c.703G>C MANE Select	NP_060017.1:p.Gly235Arg
NR_037647.2:n.535G>C
NR_037648.2:n.880G>C