Canonical Allele Identifier: CA383229979

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126144881G>A (hg19) ; chr11:g.126274986G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274986G>A , CM000673.2:g.126274986G>A	GRCh38
NC_000011.9:g.126144881G>A , CM000673.1:g.126144881G>A	GRCh37
NC_000011.8:g.125650091G>A	NCBI36
NG_028029.1:g.10947G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.774G>A
ENST00000532101.6:n.734-341G>A
ENST00000532125.2:c.593G>A	ENSP00000434178.2:p.Trp198Ter
ENST00000533839.6:c.86-808G>A	ENSP00000509952.1:n.86-808G>A
ENST00000534011.6:n.888G>A
ENST00000685484.1:c.596G>A	ENSP00000510622.1:p.Trp199Ter
ENST00000685601.1:c.596G>A	ENSP00000510603.1:p.Trp199Ter
ENST00000685765.1:c.596G>A	ENSP00000509991.1:p.Trp199Ter
ENST00000685844.1:c.*169-341G>A	ENSP00000509820.1:n.*169-341G>A
ENST00000685857.1:n.1030G>A
ENST00000686242.1:c.395G>A	ENSP00000508950.1:n.395G>A
ENST00000686888.1:c.*163G>A	ENSP00000509619.1:n.*163G>A
ENST00000687699.1:c.720G>A	ENSP00000508878.1:n.720G>A
ENST00000687786.1:n.2068-341G>A
ENST00000688100.1:n.1517G>A
ENST00000688588.1:c.596G>A	ENSP00000510802.1:p.Trp199Ter
ENST00000688927.1:n.2502G>A
ENST00000689283.1:c.*259G>A	ENSP00000509050.1:n.*259G>A
ENST00000689477.1:c.*489G>A	ENSP00000508945.1:n.*489G>A
ENST00000689765.1:c.*169-385G>A	ENSP00000509625.1:n.*169-385G>A
ENST00000690512.1:c.*447G>A	ENSP00000509793.1:n.*447G>A
ENST00000692039.1:c.*394G>A	ENSP00000508821.1:n.*394G>A
ENST00000692336.1:c.620G>A	ENSP00000508540.1:p.Trp207Ter
ENST00000693133.1:n.771G>A
ENST00000263578.10:c.596G>A MANE Select	ENSP00000263578.5:p.Trp199Ter
ENST00000263578.9:c.596G>A	ENSP00000263578.5:p.Trp199Ter
ENST00000524751.5:n.532G>A
ENST00000525083.5:n.352-341G>A
ENST00000525770.5:c.*228G>A	ENSP00000434739.1:n.*228G>A
ENST00000526366.5:n.527G>A
ENST00000527004.5:c.534-341G>A	ENSP00000436374.1:n.534-341G>A
ENST00000527875.1:n.426G>A
ENST00000530642.1:n.1073G>A
ENST00000532101.5:n.819G>A
ENST00000532125.1:c.554G>A	ENSP00000434178.1:p.Trp185Ter
ENST00000533395.5:n.365-341G>A
ENST00000533839.5:n.238-808G>A
ENST00000534011.5:n.648G>A
ENST00000534315.5:n.944-341G>A
NM_017547.3:c.596G>A	NP_060017.1:p.Trp199Ter
NR_037647.1:n.542G>A
NR_037648.1:n.782G>A
XM_006718879.2:c.86G>A	XP_006718942.1:p.Trp29Ter
XM_006718880.2:c.-2-341G>A	XP_006718943.1:n.-2-341G>A
XM_006718881.2:c.-2-341G>A	XP_006718944.1:n.-2-341G>A
XM_011542895.1:c.86G>A	XP_011541197.1:p.Trp29Ter
XM_011542896.1:c.86G>A	XP_011541198.1:p.Trp29Ter
XM_006718879.3:c.86G>A	XP_006718942.1:p.Trp29Ter
XM_006718881.3:c.-2-341G>A	XP_006718944.1:n.-2-341G>A
XM_011542895.2:c.86G>A	XP_011541197.1:p.Trp29Ter
XM_011542896.2:c.86G>A	XP_011541198.1:p.Trp29Ter
XM_017018000.2:c.596G>A	XP_016873489.1:p.Trp199Ter
XM_017018001.1:c.86G>A	XP_016873490.1:p.Trp29Ter
XM_017018002.1:c.86G>A	XP_016873491.1:p.Trp29Ter
XM_017018003.2:c.-2-341G>A	XP_016873492.1:n.-2-341G>A
XM_017018004.1:c.-2-341G>A	XP_016873493.1:n.-2-341G>A
XM_017018005.1:c.-2-341G>A	XP_016873494.1:n.-2-341G>A
XM_017018006.2:c.-2-341G>A	XP_016873495.1:n.-2-341G>A
NM_017547.4:c.596G>A MANE Select	NP_060017.1:p.Trp199Ter
NR_037647.2:n.428G>A
NR_037648.2:n.773G>A