Canonical Allele Identifier: CA383230206

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145286G>T (hg19) ; chr11:g.126275391G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275391G>T , CM000673.2:g.126275391G>T	GRCh38
NC_000011.9:g.126145286G>T , CM000673.1:g.126145286G>T	GRCh37
NC_000011.8:g.125650496G>T	NCBI36
NG_028029.1:g.11352G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000525083.6:n.1179G>T
ENST00000532101.6:n.798G>T
ENST00000532125.2:c.693G>T	ENSP00000434178.2:p.Gln231His
ENST00000533839.6:c.86-403G>T	ENSP00000509952.1:n.86-403G>T
ENST00000534011.6:n.988G>T
ENST00000685484.1:c.696G>T	ENSP00000510622.1:p.Gln232His
ENST00000685601.1:c.696G>T	ENSP00000510603.1:p.Gln232His
ENST00000685765.1:c.696G>T	ENSP00000509991.1:p.Gln232His
ENST00000685844.1:c.*233G>T	ENSP00000509820.1:n.*233G>T
ENST00000685857.1:n.1435G>T
ENST00000686242.1:c.495G>T	ENSP00000508950.1:n.495G>T
ENST00000686888.1:c.*263G>T	ENSP00000509619.1:n.*263G>T
ENST00000687699.1:c.820G>T	ENSP00000508878.1:n.820G>T
ENST00000687786.1:n.2132G>T
ENST00000688100.1:n.1617G>T
ENST00000688588.1:c.696G>T	ENSP00000510802.1:p.Gln232His
ENST00000688927.1:n.2907G>T
ENST00000689283.1:c.*359G>T	ENSP00000509050.1:n.*359G>T
ENST00000689477.1:c.*589G>T	ENSP00000508945.1:n.*589G>T
ENST00000689765.1:c.*189G>T	ENSP00000509625.1:n.*189G>T
ENST00000690512.1:c.*547G>T	ENSP00000509793.1:n.*547G>T
ENST00000692039.1:c.*494G>T	ENSP00000508821.1:n.*494G>T
ENST00000692336.1:c.720G>T	ENSP00000508540.1:p.Gln240His
ENST00000693133.1:n.1176G>T
ENST00000263578.10:c.696G>T MANE Select	ENSP00000263578.5:p.Gln232His
ENST00000263578.9:c.696G>T	ENSP00000263578.5:p.Gln232His
ENST00000525083.5:n.416G>T
ENST00000525770.5:c.*328G>T	ENSP00000434739.1:n.*328G>T
ENST00000527004.5:c.*40G>T	ENSP00000436374.1:n.*40G>T
ENST00000530642.1:n.1478G>T
ENST00000532101.5:n.919G>T
ENST00000532125.1:c.654G>T	ENSP00000434178.1:p.Gln218His
ENST00000533395.5:n.429G>T
ENST00000533839.5:n.238-403G>T
ENST00000534011.5:n.748G>T
ENST00000534315.5:n.1008G>T
NM_017547.3:c.696G>T	NP_060017.1:p.Gln232His
NR_037647.1:n.642G>T
NR_037648.1:n.882G>T
XM_006718879.2:c.186G>T	XP_006718942.1:p.Gln62His
XM_006718880.2:c.63G>T	XP_006718943.1:p.Gln21His
XM_006718881.2:c.63G>T	XP_006718944.1:p.Gln21His
XM_011542895.1:c.186G>T	XP_011541197.1:p.Gln62His
XM_011542896.1:c.186G>T	XP_011541198.1:p.Gln62His
XM_006718879.3:c.186G>T	XP_006718942.1:p.Gln62His
XM_006718881.3:c.63G>T	XP_006718944.1:p.Gln21His
XM_011542895.2:c.186G>T	XP_011541197.1:p.Gln62His
XM_011542896.2:c.186G>T	XP_011541198.1:p.Gln62His
XM_017018000.2:c.696G>T	XP_016873489.1:p.Gln232His
XM_017018001.1:c.186G>T	XP_016873490.1:p.Gln62His
XM_017018002.1:c.186G>T	XP_016873491.1:p.Gln62His
XM_017018003.2:c.63G>T	XP_016873492.1:p.Gln21His
XM_017018004.1:c.63G>T	XP_016873493.1:p.Gln21His
XM_017018005.1:c.63G>T	XP_016873494.1:p.Gln21His
XM_017018006.2:c.63G>T	XP_016873495.1:p.Gln21His
NM_017547.4:c.696G>T MANE Select	NP_060017.1:p.Gln232His
NR_037647.2:n.528G>T
NR_037648.2:n.873G>T