Canonical Allele Identifier: CA477515354

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126144900G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275005G>T , CM000673.2:g.126275005G>T	GRCh38
NC_000011.9:g.126144900G>T , CM000673.1:g.126144900G>T	GRCh37
NC_000011.8:g.125650110G>T	NCBI36
NG_028029.1:g.10966G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.793G>T
ENST00000532101.6:n.734-322G>T
ENST00000532125.2:c.612G>T	ENSP00000434178.2:p.Val204=
ENST00000533839.6:c.86-789G>T	ENSP00000509952.1:n.86-789G>T
ENST00000534011.6:n.907G>T
ENST00000685484.1:c.615G>T	ENSP00000510622.1:p.Val205=
ENST00000685601.1:c.615G>T	ENSP00000510603.1:p.Val205=
ENST00000685765.1:c.615G>T	ENSP00000509991.1:p.Val205=
ENST00000685844.1:c.*169-322G>T	ENSP00000509820.1:n.*169-322G>T
ENST00000685857.1:n.1049G>T
ENST00000686242.1:c.414G>T	ENSP00000508950.1:n.414G>T
ENST00000686888.1:c.*182G>T	ENSP00000509619.1:n.*182G>T
ENST00000687699.1:c.739G>T	ENSP00000508878.1:n.739G>T
ENST00000687786.1:n.2068-322G>T
ENST00000688100.1:n.1536G>T
ENST00000688588.1:c.615G>T	ENSP00000510802.1:p.Val205=
ENST00000688927.1:n.2521G>T
ENST00000689283.1:c.*278G>T	ENSP00000509050.1:n.*278G>T
ENST00000689477.1:c.*508G>T	ENSP00000508945.1:n.*508G>T
ENST00000689765.1:c.*169-366G>T	ENSP00000509625.1:n.*169-366G>T
ENST00000690512.1:c.*466G>T	ENSP00000509793.1:n.*466G>T
ENST00000692039.1:c.*413G>T	ENSP00000508821.1:n.*413G>T
ENST00000692336.1:c.639G>T	ENSP00000508540.1:p.Val213=
ENST00000693133.1:n.790G>T
ENST00000263578.10:c.615G>T MANE Select	ENSP00000263578.5:p.Val205=
ENST00000263578.9:c.615G>T	ENSP00000263578.5:p.Val205=
ENST00000524751.5:n.551G>T
ENST00000525083.5:n.352-322G>T
ENST00000525770.5:c.*247G>T	ENSP00000434739.1:n.*247G>T
ENST00000526366.5:n.546G>T
ENST00000527004.5:c.534-322G>T	ENSP00000436374.1:n.534-322G>T
ENST00000527875.1:n.445G>T
ENST00000530642.1:n.1092G>T
ENST00000532101.5:n.838G>T
ENST00000532125.1:c.573G>T	ENSP00000434178.1:p.Val191=
ENST00000533395.5:n.365-322G>T
ENST00000533839.5:n.238-789G>T
ENST00000534011.5:n.667G>T
ENST00000534315.5:n.944-322G>T
NM_017547.3:c.615G>T	NP_060017.1:p.Val205=
NR_037647.1:n.561G>T
NR_037648.1:n.801G>T
XM_006718879.2:c.105G>T	XP_006718942.1:p.Val35=
XM_006718880.2:c.-2-322G>T	XP_006718943.1:n.-2-322G>T
XM_006718881.2:c.-2-322G>T	XP_006718944.1:n.-2-322G>T
XM_011542895.1:c.105G>T	XP_011541197.1:p.Val35=
XM_011542896.1:c.105G>T	XP_011541198.1:p.Val35=
XM_006718879.3:c.105G>T	XP_006718942.1:p.Val35=
XM_006718881.3:c.-2-322G>T	XP_006718944.1:n.-2-322G>T
XM_011542895.2:c.105G>T	XP_011541197.1:p.Val35=
XM_011542896.2:c.105G>T	XP_011541198.1:p.Val35=
XM_017018000.2:c.615G>T	XP_016873489.1:p.Val205=
XM_017018001.1:c.105G>T	XP_016873490.1:p.Val35=
XM_017018002.1:c.105G>T	XP_016873491.1:p.Val35=
XM_017018003.2:c.-2-322G>T	XP_016873492.1:n.-2-322G>T
XM_017018004.1:c.-2-322G>T	XP_016873493.1:n.-2-322G>T
XM_017018005.1:c.-2-322G>T	XP_016873494.1:n.-2-322G>T
XM_017018006.2:c.-2-322G>T	XP_016873495.1:n.-2-322G>T
NM_017547.4:c.615G>T MANE Select	NP_060017.1:p.Val205=
NR_037647.2:n.447G>T
NR_037648.2:n.792G>T