Canonical Allele Identifier: CA383229877

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126144832G>T (hg19) ; chr11:g.126274937G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274937G>T , CM000673.2:g.126274937G>T	GRCh38
NC_000011.9:g.126144832G>T , CM000673.1:g.126144832G>T	GRCh37
NC_000011.8:g.125650042G>T	NCBI36
NG_028029.1:g.10898G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.725G>T
ENST00000532101.6:n.734-390G>T
ENST00000532125.2:c.544G>T	ENSP00000434178.2:p.Ala182Ser
ENST00000533839.6:c.86-857G>T	ENSP00000509952.1:n.86-857G>T
ENST00000534011.6:n.839G>T
ENST00000685484.1:c.547G>T	ENSP00000510622.1:p.Ala183Ser
ENST00000685601.1:c.547G>T	ENSP00000510603.1:p.Ala183Ser
ENST00000685765.1:c.547G>T	ENSP00000509991.1:p.Ala183Ser
ENST00000685844.1:c.*169-390G>T	ENSP00000509820.1:n.*169-390G>T
ENST00000685857.1:n.981G>T
ENST00000686242.1:c.346G>T	ENSP00000508950.1:n.346G>T
ENST00000686888.1:c.*114G>T	ENSP00000509619.1:n.*114G>T
ENST00000687699.1:c.671G>T	ENSP00000508878.1:n.671G>T
ENST00000687786.1:n.2068-390G>T
ENST00000688100.1:n.1468G>T
ENST00000688588.1:c.547G>T	ENSP00000510802.1:p.Ala183Ser
ENST00000688927.1:n.2453G>T
ENST00000689283.1:c.*210G>T	ENSP00000509050.1:n.*210G>T
ENST00000689477.1:c.*440G>T	ENSP00000508945.1:n.*440G>T
ENST00000689765.1:c.*169-434G>T	ENSP00000509625.1:n.*169-434G>T
ENST00000690512.1:c.*398G>T	ENSP00000509793.1:n.*398G>T
ENST00000692039.1:c.*345G>T	ENSP00000508821.1:n.*345G>T
ENST00000692336.1:c.571G>T	ENSP00000508540.1:p.Ala191Ser
ENST00000693133.1:n.722G>T
ENST00000263578.10:c.547G>T MANE Select	ENSP00000263578.5:p.Ala183Ser
ENST00000263578.9:c.547G>T	ENSP00000263578.5:p.Ala183Ser
ENST00000524751.5:n.483G>T
ENST00000525083.5:n.352-390G>T
ENST00000525770.5:c.*179G>T	ENSP00000434739.1:n.*179G>T
ENST00000526366.5:n.478G>T
ENST00000527004.5:c.534-390G>T	ENSP00000436374.1:n.534-390G>T
ENST00000527875.1:n.377G>T
ENST00000530642.1:n.1024G>T
ENST00000532101.5:n.770G>T
ENST00000532125.1:c.505G>T	ENSP00000434178.1:p.Ala169Ser
ENST00000533395.5:n.365-390G>T
ENST00000533839.5:n.238-857G>T
ENST00000534011.5:n.599G>T
ENST00000534315.5:n.944-390G>T
NM_017547.3:c.547G>T	NP_060017.1:p.Ala183Ser
NR_037647.1:n.493G>T
NR_037648.1:n.733G>T
XM_006718879.2:c.37G>T	XP_006718942.1:p.Ala13Ser
XM_006718880.2:c.-2-390G>T	XP_006718943.1:n.-2-390G>T
XM_006718881.2:c.-2-390G>T	XP_006718944.1:n.-2-390G>T
XM_011542895.1:c.37G>T	XP_011541197.1:p.Ala13Ser
XM_011542896.1:c.37G>T	XP_011541198.1:p.Ala13Ser
XM_006718879.3:c.37G>T	XP_006718942.1:p.Ala13Ser
XM_006718881.3:c.-2-390G>T	XP_006718944.1:n.-2-390G>T
XM_011542895.2:c.37G>T	XP_011541197.1:p.Ala13Ser
XM_011542896.2:c.37G>T	XP_011541198.1:p.Ala13Ser
XM_017018000.2:c.547G>T	XP_016873489.1:p.Ala183Ser
XM_017018001.1:c.37G>T	XP_016873490.1:p.Ala13Ser
XM_017018002.1:c.37G>T	XP_016873491.1:p.Ala13Ser
XM_017018003.2:c.-2-390G>T	XP_016873492.1:n.-2-390G>T
XM_017018004.1:c.-2-390G>T	XP_016873493.1:n.-2-390G>T
XM_017018005.1:c.-2-390G>T	XP_016873494.1:n.-2-390G>T
XM_017018006.2:c.-2-390G>T	XP_016873495.1:n.-2-390G>T
NM_017547.4:c.547G>T MANE Select	NP_060017.1:p.Ala183Ser
NR_037647.2:n.379G>T
NR_037648.2:n.724G>T