Canonical Allele Identifier: CA383230082

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145227G>T (hg19) ; chr11:g.126275332G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275332G>T , CM000673.2:g.126275332G>T	GRCh38
NC_000011.9:g.126145227G>T , CM000673.1:g.126145227G>T	GRCh37
NC_000011.8:g.125650437G>T	NCBI36
NG_028029.1:g.11293G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1120G>T
ENST00000532101.6:n.739G>T
ENST00000532125.2:c.634G>T	ENSP00000434178.2:p.Glu212Ter
ENST00000533839.6:c.86-462G>T	ENSP00000509952.1:n.86-462G>T
ENST00000534011.6:n.929G>T
ENST00000685484.1:c.637G>T	ENSP00000510622.1:p.Glu213Ter
ENST00000685601.1:c.637G>T	ENSP00000510603.1:p.Glu213Ter
ENST00000685765.1:c.637G>T	ENSP00000509991.1:p.Glu213Ter
ENST00000685844.1:c.*174G>T	ENSP00000509820.1:n.*174G>T
ENST00000685857.1:n.1376G>T
ENST00000686242.1:c.436G>T	ENSP00000508950.1:n.436G>T
ENST00000686888.1:c.*204G>T	ENSP00000509619.1:n.*204G>T
ENST00000687699.1:c.761G>T	ENSP00000508878.1:n.761G>T
ENST00000687786.1:n.2073G>T
ENST00000688100.1:n.1558G>T
ENST00000688588.1:c.637G>T	ENSP00000510802.1:p.Glu213Ter
ENST00000688927.1:n.2848G>T
ENST00000689283.1:c.*300G>T	ENSP00000509050.1:n.*300G>T
ENST00000689477.1:c.*530G>T	ENSP00000508945.1:n.*530G>T
ENST00000689765.1:c.*169-39G>T	ENSP00000509625.1:n.*169-39G>T
ENST00000690512.1:c.*488G>T	ENSP00000509793.1:n.*488G>T
ENST00000692039.1:c.*435G>T	ENSP00000508821.1:n.*435G>T
ENST00000692336.1:c.661G>T	ENSP00000508540.1:p.Glu221Ter
ENST00000693133.1:n.1117G>T
ENST00000263578.10:c.637G>T MANE Select	ENSP00000263578.5:p.Glu213Ter
ENST00000263578.9:c.637G>T	ENSP00000263578.5:p.Glu213Ter
ENST00000524751.5:n.878G>T
ENST00000525083.5:n.357G>T
ENST00000525770.5:c.*269G>T	ENSP00000434739.1:n.*269G>T
ENST00000527004.5:c.539G>T	ENSP00000436374.1:p.Gly180Val
ENST00000530642.1:n.1419G>T
ENST00000532101.5:n.860G>T
ENST00000532125.1:c.595G>T	ENSP00000434178.1:p.Glu199Ter
ENST00000533395.5:n.370G>T
ENST00000533839.5:n.238-462G>T
ENST00000534011.5:n.689G>T
ENST00000534315.5:n.949G>T
NM_017547.3:c.637G>T	NP_060017.1:p.Glu213Ter
NR_037647.1:n.583G>T
NR_037648.1:n.823G>T
XM_006718879.2:c.127G>T	XP_006718942.1:p.Glu43Ter
XM_006718880.2:c.4G>T	XP_006718943.1:p.Glu2Ter
XM_006718881.2:c.4G>T	XP_006718944.1:p.Glu2Ter
XM_011542895.1:c.127G>T	XP_011541197.1:p.Glu43Ter
XM_011542896.1:c.127G>T	XP_011541198.1:p.Glu43Ter
XM_006718879.3:c.127G>T	XP_006718942.1:p.Glu43Ter
XM_006718881.3:c.4G>T	XP_006718944.1:p.Glu2Ter
XM_011542895.2:c.127G>T	XP_011541197.1:p.Glu43Ter
XM_011542896.2:c.127G>T	XP_011541198.1:p.Glu43Ter
XM_017018000.2:c.637G>T	XP_016873489.1:p.Glu213Ter
XM_017018001.1:c.127G>T	XP_016873490.1:p.Glu43Ter
XM_017018002.1:c.127G>T	XP_016873491.1:p.Glu43Ter
XM_017018003.2:c.4G>T	XP_016873492.1:p.Glu2Ter
XM_017018004.1:c.4G>T	XP_016873493.1:p.Glu2Ter
XM_017018005.1:c.4G>T	XP_016873494.1:p.Glu2Ter
XM_017018006.2:c.4G>T	XP_016873495.1:p.Glu2Ter
NM_017547.4:c.637G>T MANE Select	NP_060017.1:p.Glu213Ter
NR_037647.2:n.469G>T
NR_037648.2:n.814G>T