Canonical Allele Identifier: CA383230227

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145297T>C (hg19) ; chr11:g.126275402T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275402T>C , CM000673.2:g.126275402T>C	GRCh38
NC_000011.9:g.126145297T>C , CM000673.1:g.126145297T>C	GRCh37
NC_000011.8:g.125650507T>C	NCBI36
NG_028029.1:g.11363T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000525083.6:n.1190T>C
ENST00000532101.6:n.809T>C
ENST00000532125.2:c.704T>C	ENSP00000434178.2:p.Val235Ala
ENST00000533839.6:c.86-392T>C	ENSP00000509952.1:n.86-392T>C
ENST00000534011.6:n.999T>C
ENST00000685484.1:c.707T>C	ENSP00000510622.1:p.Val236Ala
ENST00000685601.1:c.707T>C	ENSP00000510603.1:p.Val236Ala
ENST00000685765.1:c.707T>C	ENSP00000509991.1:p.Val236Ala
ENST00000685844.1:c.*244T>C	ENSP00000509820.1:n.*244T>C
ENST00000685857.1:n.1446T>C
ENST00000686242.1:c.506T>C	ENSP00000508950.1:n.506T>C
ENST00000686888.1:c.*274T>C	ENSP00000509619.1:n.*274T>C
ENST00000687699.1:c.831T>C	ENSP00000508878.1:n.831T>C
ENST00000687786.1:n.2143T>C
ENST00000688100.1:n.1628T>C
ENST00000688588.1:c.707T>C	ENSP00000510802.1:p.Val236Ala
ENST00000688927.1:n.2918T>C
ENST00000689283.1:c.*370T>C	ENSP00000509050.1:n.*370T>C
ENST00000689477.1:c.*600T>C	ENSP00000508945.1:n.*600T>C
ENST00000689765.1:c.*200T>C	ENSP00000509625.1:n.*200T>C
ENST00000690512.1:c.*558T>C	ENSP00000509793.1:n.*558T>C
ENST00000692039.1:c.*505T>C	ENSP00000508821.1:n.*505T>C
ENST00000692336.1:c.731T>C	ENSP00000508540.1:p.Val244Ala
ENST00000693133.1:n.1187T>C
ENST00000263578.10:c.707T>C MANE Select	ENSP00000263578.5:p.Val236Ala
ENST00000263578.9:c.707T>C	ENSP00000263578.5:p.Val236Ala
ENST00000525083.5:n.427T>C
ENST00000525770.5:c.*339T>C	ENSP00000434739.1:n.*339T>C
ENST00000527004.5:c.*51T>C	ENSP00000436374.1:n.*51T>C
ENST00000530642.1:n.1489T>C
ENST00000532101.5:n.930T>C
ENST00000532125.1:c.665T>C	ENSP00000434178.1:p.Val222Ala
ENST00000533395.5:n.440T>C
ENST00000533839.5:n.238-392T>C
ENST00000534011.5:n.759T>C
ENST00000534315.5:n.1019T>C
NM_017547.3:c.707T>C	NP_060017.1:p.Val236Ala
NR_037647.1:n.653T>C
NR_037648.1:n.893T>C
XM_006718879.2:c.197T>C	XP_006718942.1:p.Val66Ala
XM_006718880.2:c.74T>C	XP_006718943.1:p.Val25Ala
XM_006718881.2:c.74T>C	XP_006718944.1:p.Val25Ala
XM_011542895.1:c.197T>C	XP_011541197.1:p.Val66Ala
XM_011542896.1:c.197T>C	XP_011541198.1:p.Val66Ala
XM_006718879.3:c.197T>C	XP_006718942.1:p.Val66Ala
XM_006718881.3:c.74T>C	XP_006718944.1:p.Val25Ala
XM_011542895.2:c.197T>C	XP_011541197.1:p.Val66Ala
XM_011542896.2:c.197T>C	XP_011541198.1:p.Val66Ala
XM_017018000.2:c.707T>C	XP_016873489.1:p.Val236Ala
XM_017018001.1:c.197T>C	XP_016873490.1:p.Val66Ala
XM_017018002.1:c.197T>C	XP_016873491.1:p.Val66Ala
XM_017018003.2:c.74T>C	XP_016873492.1:p.Val25Ala
XM_017018004.1:c.74T>C	XP_016873493.1:p.Val25Ala
XM_017018005.1:c.74T>C	XP_016873494.1:p.Val25Ala
XM_017018006.2:c.74T>C	XP_016873495.1:p.Val25Ala
NM_017547.4:c.707T>C MANE Select	NP_060017.1:p.Val236Ala
NR_037647.2:n.539T>C
NR_037648.2:n.884T>C