Canonical Allele Identifier: CA383230024

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126144901G>T (hg19) ; chr11:g.126275006G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275006G>T , CM000673.2:g.126275006G>T	GRCh38
NC_000011.9:g.126144901G>T , CM000673.1:g.126144901G>T	GRCh37
NC_000011.8:g.125650111G>T	NCBI36
NG_028029.1:g.10967G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.794G>T
ENST00000532101.6:n.734-321G>T
ENST00000532125.2:c.613G>T	ENSP00000434178.2:p.Ala205Ser
ENST00000533839.6:c.86-788G>T	ENSP00000509952.1:n.86-788G>T
ENST00000534011.6:n.908G>T
ENST00000685484.1:c.616G>T	ENSP00000510622.1:p.Ala206Ser
ENST00000685601.1:c.616G>T	ENSP00000510603.1:p.Ala206Ser
ENST00000685765.1:c.616G>T	ENSP00000509991.1:p.Ala206Ser
ENST00000685844.1:c.*169-321G>T	ENSP00000509820.1:n.*169-321G>T
ENST00000685857.1:n.1050G>T
ENST00000686242.1:c.415G>T	ENSP00000508950.1:n.415G>T
ENST00000686888.1:c.*183G>T	ENSP00000509619.1:n.*183G>T
ENST00000687699.1:c.740G>T	ENSP00000508878.1:n.740G>T
ENST00000687786.1:n.2068-321G>T
ENST00000688100.1:n.1537G>T
ENST00000688588.1:c.616G>T	ENSP00000510802.1:p.Ala206Ser
ENST00000688927.1:n.2522G>T
ENST00000689283.1:c.*279G>T	ENSP00000509050.1:n.*279G>T
ENST00000689477.1:c.*509G>T	ENSP00000508945.1:n.*509G>T
ENST00000689765.1:c.*169-365G>T	ENSP00000509625.1:n.*169-365G>T
ENST00000690512.1:c.*467G>T	ENSP00000509793.1:n.*467G>T
ENST00000692039.1:c.*414G>T	ENSP00000508821.1:n.*414G>T
ENST00000692336.1:c.640G>T	ENSP00000508540.1:p.Ala214Ser
ENST00000693133.1:n.791G>T
ENST00000263578.10:c.616G>T MANE Select	ENSP00000263578.5:p.Ala206Ser
ENST00000263578.9:c.616G>T	ENSP00000263578.5:p.Ala206Ser
ENST00000524751.5:n.552G>T
ENST00000525083.5:n.352-321G>T
ENST00000525770.5:c.*248G>T	ENSP00000434739.1:n.*248G>T
ENST00000526366.5:n.547G>T
ENST00000527004.5:c.534-321G>T	ENSP00000436374.1:n.534-321G>T
ENST00000527875.1:n.446G>T
ENST00000530642.1:n.1093G>T
ENST00000532101.5:n.839G>T
ENST00000532125.1:c.574G>T	ENSP00000434178.1:p.Ala192Ser
ENST00000533395.5:n.365-321G>T
ENST00000533839.5:n.238-788G>T
ENST00000534011.5:n.668G>T
ENST00000534315.5:n.944-321G>T
NM_017547.3:c.616G>T	NP_060017.1:p.Ala206Ser
NR_037647.1:n.562G>T
NR_037648.1:n.802G>T
XM_006718879.2:c.106G>T	XP_006718942.1:p.Ala36Ser
XM_006718880.2:c.-2-321G>T	XP_006718943.1:n.-2-321G>T
XM_006718881.2:c.-2-321G>T	XP_006718944.1:n.-2-321G>T
XM_011542895.1:c.106G>T	XP_011541197.1:p.Ala36Ser
XM_011542896.1:c.106G>T	XP_011541198.1:p.Ala36Ser
XM_006718879.3:c.106G>T	XP_006718942.1:p.Ala36Ser
XM_006718881.3:c.-2-321G>T	XP_006718944.1:n.-2-321G>T
XM_011542895.2:c.106G>T	XP_011541197.1:p.Ala36Ser
XM_011542896.2:c.106G>T	XP_011541198.1:p.Ala36Ser
XM_017018000.2:c.616G>T	XP_016873489.1:p.Ala206Ser
XM_017018001.1:c.106G>T	XP_016873490.1:p.Ala36Ser
XM_017018002.1:c.106G>T	XP_016873491.1:p.Ala36Ser
XM_017018003.2:c.-2-321G>T	XP_016873492.1:n.-2-321G>T
XM_017018004.1:c.-2-321G>T	XP_016873493.1:n.-2-321G>T
XM_017018005.1:c.-2-321G>T	XP_016873494.1:n.-2-321G>T
XM_017018006.2:c.-2-321G>T	XP_016873495.1:n.-2-321G>T
NM_017547.4:c.616G>T MANE Select	NP_060017.1:p.Ala206Ser
NR_037647.2:n.448G>T
NR_037648.2:n.793G>T