Canonical Allele Identifier: CA383230128

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145246A>C (hg19) ; chr11:g.126275351A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275351A>C , CM000673.2:g.126275351A>C	GRCh38
NC_000011.9:g.126145246A>C , CM000673.1:g.126145246A>C	GRCh37
NC_000011.8:g.125650456A>C	NCBI36
NG_028029.1:g.11312A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1139A>C
ENST00000532101.6:n.758A>C
ENST00000532125.2:c.653A>C	ENSP00000434178.2:p.Asp218Ala
ENST00000533839.6:c.86-443A>C	ENSP00000509952.1:n.86-443A>C
ENST00000534011.6:n.948A>C
ENST00000685484.1:c.656A>C	ENSP00000510622.1:p.Asp219Ala
ENST00000685601.1:c.656A>C	ENSP00000510603.1:p.Asp219Ala
ENST00000685765.1:c.656A>C	ENSP00000509991.1:p.Asp219Ala
ENST00000685844.1:c.*193A>C	ENSP00000509820.1:n.*193A>C
ENST00000685857.1:n.1395A>C
ENST00000686242.1:c.455A>C	ENSP00000508950.1:n.455A>C
ENST00000686888.1:c.*223A>C	ENSP00000509619.1:n.*223A>C
ENST00000687699.1:c.780A>C	ENSP00000508878.1:n.780A>C
ENST00000687786.1:n.2092A>C
ENST00000688100.1:n.1577A>C
ENST00000688588.1:c.656A>C	ENSP00000510802.1:p.Asp219Ala
ENST00000688927.1:n.2867A>C
ENST00000689283.1:c.*319A>C	ENSP00000509050.1:n.*319A>C
ENST00000689477.1:c.*549A>C	ENSP00000508945.1:n.*549A>C
ENST00000689765.1:c.*169-20A>C	ENSP00000509625.1:n.*169-20A>C
ENST00000690512.1:c.*507A>C	ENSP00000509793.1:n.*507A>C
ENST00000692039.1:c.*454A>C	ENSP00000508821.1:n.*454A>C
ENST00000692336.1:c.680A>C	ENSP00000508540.1:p.Asp227Ala
ENST00000693133.1:n.1136A>C
ENST00000263578.10:c.656A>C MANE Select	ENSP00000263578.5:p.Asp219Ala
ENST00000263578.9:c.656A>C	ENSP00000263578.5:p.Asp219Ala
ENST00000525083.5:n.376A>C
ENST00000525770.5:c.*288A>C	ENSP00000434739.1:n.*288A>C
ENST00000527004.5:c.558A>C	ENSP00000436374.1:p.Ter186Cys
ENST00000530642.1:n.1438A>C
ENST00000532101.5:n.879A>C
ENST00000532125.1:c.614A>C	ENSP00000434178.1:p.Asp205Ala
ENST00000533395.5:n.389A>C
ENST00000533839.5:n.238-443A>C
ENST00000534011.5:n.708A>C
ENST00000534315.5:n.968A>C
NM_017547.3:c.656A>C	NP_060017.1:p.Asp219Ala
NR_037647.1:n.602A>C
NR_037648.1:n.842A>C
XM_006718879.2:c.146A>C	XP_006718942.1:p.Asp49Ala
XM_006718880.2:c.23A>C	XP_006718943.1:p.Asp8Ala
XM_006718881.2:c.23A>C	XP_006718944.1:p.Asp8Ala
XM_011542895.1:c.146A>C	XP_011541197.1:p.Asp49Ala
XM_011542896.1:c.146A>C	XP_011541198.1:p.Asp49Ala
XM_006718879.3:c.146A>C	XP_006718942.1:p.Asp49Ala
XM_006718881.3:c.23A>C	XP_006718944.1:p.Asp8Ala
XM_011542895.2:c.146A>C	XP_011541197.1:p.Asp49Ala
XM_011542896.2:c.146A>C	XP_011541198.1:p.Asp49Ala
XM_017018000.2:c.656A>C	XP_016873489.1:p.Asp219Ala
XM_017018001.1:c.146A>C	XP_016873490.1:p.Asp49Ala
XM_017018002.1:c.146A>C	XP_016873491.1:p.Asp49Ala
XM_017018003.2:c.23A>C	XP_016873492.1:p.Asp8Ala
XM_017018004.1:c.23A>C	XP_016873493.1:p.Asp8Ala
XM_017018005.1:c.23A>C	XP_016873494.1:p.Asp8Ala
XM_017018006.2:c.23A>C	XP_016873495.1:p.Asp8Ala
NM_017547.4:c.656A>C MANE Select	NP_060017.1:p.Asp219Ala
NR_037647.2:n.488A>C
NR_037648.2:n.833A>C