Canonical Allele Identifier: CA383230126

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145245G>T (hg19) ; chr11:g.126275350G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275350G>T , CM000673.2:g.126275350G>T	GRCh38
NC_000011.9:g.126145245G>T , CM000673.1:g.126145245G>T	GRCh37
NC_000011.8:g.125650455G>T	NCBI36
NG_028029.1:g.11311G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1138G>T
ENST00000532101.6:n.757G>T
ENST00000532125.2:c.652G>T	ENSP00000434178.2:p.Asp218Tyr
ENST00000533839.6:c.86-444G>T	ENSP00000509952.1:n.86-444G>T
ENST00000534011.6:n.947G>T
ENST00000685484.1:c.655G>T	ENSP00000510622.1:p.Asp219Tyr
ENST00000685601.1:c.655G>T	ENSP00000510603.1:p.Asp219Tyr
ENST00000685765.1:c.655G>T	ENSP00000509991.1:p.Asp219Tyr
ENST00000685844.1:c.*192G>T	ENSP00000509820.1:n.*192G>T
ENST00000685857.1:n.1394G>T
ENST00000686242.1:c.454G>T	ENSP00000508950.1:n.454G>T
ENST00000686888.1:c.*222G>T	ENSP00000509619.1:n.*222G>T
ENST00000687699.1:c.779G>T	ENSP00000508878.1:n.779G>T
ENST00000687786.1:n.2091G>T
ENST00000688100.1:n.1576G>T
ENST00000688588.1:c.655G>T	ENSP00000510802.1:p.Asp219Tyr
ENST00000688927.1:n.2866G>T
ENST00000689283.1:c.*318G>T	ENSP00000509050.1:n.*318G>T
ENST00000689477.1:c.*548G>T	ENSP00000508945.1:n.*548G>T
ENST00000689765.1:c.*169-21G>T	ENSP00000509625.1:n.*169-21G>T
ENST00000690512.1:c.*506G>T	ENSP00000509793.1:n.*506G>T
ENST00000692039.1:c.*453G>T	ENSP00000508821.1:n.*453G>T
ENST00000692336.1:c.679G>T	ENSP00000508540.1:p.Asp227Tyr
ENST00000693133.1:n.1135G>T
ENST00000263578.10:c.655G>T MANE Select	ENSP00000263578.5:p.Asp219Tyr
ENST00000263578.9:c.655G>T	ENSP00000263578.5:p.Asp219Tyr
ENST00000525083.5:n.375G>T
ENST00000525770.5:c.*287G>T	ENSP00000434739.1:n.*287G>T
ENST00000527004.5:c.557G>T	ENSP00000436374.1:p.Ter186Leu
ENST00000530642.1:n.1437G>T
ENST00000532101.5:n.878G>T
ENST00000532125.1:c.613G>T	ENSP00000434178.1:p.Asp205Tyr
ENST00000533395.5:n.388G>T
ENST00000533839.5:n.238-444G>T
ENST00000534011.5:n.707G>T
ENST00000534315.5:n.967G>T
NM_017547.3:c.655G>T	NP_060017.1:p.Asp219Tyr
NR_037647.1:n.601G>T
NR_037648.1:n.841G>T
XM_006718879.2:c.145G>T	XP_006718942.1:p.Asp49Tyr
XM_006718880.2:c.22G>T	XP_006718943.1:p.Asp8Tyr
XM_006718881.2:c.22G>T	XP_006718944.1:p.Asp8Tyr
XM_011542895.1:c.145G>T	XP_011541197.1:p.Asp49Tyr
XM_011542896.1:c.145G>T	XP_011541198.1:p.Asp49Tyr
XM_006718879.3:c.145G>T	XP_006718942.1:p.Asp49Tyr
XM_006718881.3:c.22G>T	XP_006718944.1:p.Asp8Tyr
XM_011542895.2:c.145G>T	XP_011541197.1:p.Asp49Tyr
XM_011542896.2:c.145G>T	XP_011541198.1:p.Asp49Tyr
XM_017018000.2:c.655G>T	XP_016873489.1:p.Asp219Tyr
XM_017018001.1:c.145G>T	XP_016873490.1:p.Asp49Tyr
XM_017018002.1:c.145G>T	XP_016873491.1:p.Asp49Tyr
XM_017018003.2:c.22G>T	XP_016873492.1:p.Asp8Tyr
XM_017018004.1:c.22G>T	XP_016873493.1:p.Asp8Tyr
XM_017018005.1:c.22G>T	XP_016873494.1:p.Asp8Tyr
XM_017018006.2:c.22G>T	XP_016873495.1:p.Asp8Tyr
NM_017547.4:c.655G>T MANE Select	NP_060017.1:p.Asp219Tyr
NR_037647.2:n.487G>T
NR_037648.2:n.832G>T