Canonical Allele Identifier: CA383229911

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126144849G>C (hg19) ; chr11:g.126274954G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274954G>C , CM000673.2:g.126274954G>C	GRCh38
NC_000011.9:g.126144849G>C , CM000673.1:g.126144849G>C	GRCh37
NC_000011.8:g.125650059G>C	NCBI36
NG_028029.1:g.10915G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.742G>C
ENST00000532101.6:n.734-373G>C
ENST00000532125.2:c.561G>C	ENSP00000434178.2:p.Met187Ile
ENST00000533839.6:c.86-840G>C	ENSP00000509952.1:n.86-840G>C
ENST00000534011.6:n.856G>C
ENST00000685484.1:c.564G>C	ENSP00000510622.1:p.Met188Ile
ENST00000685601.1:c.564G>C	ENSP00000510603.1:p.Met188Ile
ENST00000685765.1:c.564G>C	ENSP00000509991.1:p.Met188Ile
ENST00000685844.1:c.*169-373G>C	ENSP00000509820.1:n.*169-373G>C
ENST00000685857.1:n.998G>C
ENST00000686242.1:c.363G>C	ENSP00000508950.1:n.363G>C
ENST00000686888.1:c.*131G>C	ENSP00000509619.1:n.*131G>C
ENST00000687699.1:c.688G>C	ENSP00000508878.1:n.688G>C
ENST00000687786.1:n.2068-373G>C
ENST00000688100.1:n.1485G>C
ENST00000688588.1:c.564G>C	ENSP00000510802.1:p.Met188Ile
ENST00000688927.1:n.2470G>C
ENST00000689283.1:c.*227G>C	ENSP00000509050.1:n.*227G>C
ENST00000689477.1:c.*457G>C	ENSP00000508945.1:n.*457G>C
ENST00000689765.1:c.*169-417G>C	ENSP00000509625.1:n.*169-417G>C
ENST00000690512.1:c.*415G>C	ENSP00000509793.1:n.*415G>C
ENST00000692039.1:c.*362G>C	ENSP00000508821.1:n.*362G>C
ENST00000692336.1:c.588G>C	ENSP00000508540.1:p.Met196Ile
ENST00000693133.1:n.739G>C
ENST00000263578.10:c.564G>C MANE Select	ENSP00000263578.5:p.Met188Ile
ENST00000263578.9:c.564G>C	ENSP00000263578.5:p.Met188Ile
ENST00000524751.5:n.500G>C
ENST00000525083.5:n.352-373G>C
ENST00000525770.5:c.*196G>C	ENSP00000434739.1:n.*196G>C
ENST00000526366.5:n.495G>C
ENST00000527004.5:c.534-373G>C	ENSP00000436374.1:n.534-373G>C
ENST00000527875.1:n.394G>C
ENST00000530642.1:n.1041G>C
ENST00000532101.5:n.787G>C
ENST00000532125.1:c.522G>C	ENSP00000434178.1:p.Met174Ile
ENST00000533395.5:n.365-373G>C
ENST00000533839.5:n.238-840G>C
ENST00000534011.5:n.616G>C
ENST00000534315.5:n.944-373G>C
NM_017547.3:c.564G>C	NP_060017.1:p.Met188Ile
NR_037647.1:n.510G>C
NR_037648.1:n.750G>C
XM_006718879.2:c.54G>C	XP_006718942.1:p.Met18Ile
XM_006718880.2:c.-2-373G>C	XP_006718943.1:n.-2-373G>C
XM_006718881.2:c.-2-373G>C	XP_006718944.1:n.-2-373G>C
XM_011542895.1:c.54G>C	XP_011541197.1:p.Met18Ile
XM_011542896.1:c.54G>C	XP_011541198.1:p.Met18Ile
XM_006718879.3:c.54G>C	XP_006718942.1:p.Met18Ile
XM_006718881.3:c.-2-373G>C	XP_006718944.1:n.-2-373G>C
XM_011542895.2:c.54G>C	XP_011541197.1:p.Met18Ile
XM_011542896.2:c.54G>C	XP_011541198.1:p.Met18Ile
XM_017018000.2:c.564G>C	XP_016873489.1:p.Met188Ile
XM_017018001.1:c.54G>C	XP_016873490.1:p.Met18Ile
XM_017018002.1:c.54G>C	XP_016873491.1:p.Met18Ile
XM_017018003.2:c.-2-373G>C	XP_016873492.1:n.-2-373G>C
XM_017018004.1:c.-2-373G>C	XP_016873493.1:n.-2-373G>C
XM_017018005.1:c.-2-373G>C	XP_016873494.1:n.-2-373G>C
XM_017018006.2:c.-2-373G>C	XP_016873495.1:n.-2-373G>C
NM_017547.4:c.564G>C MANE Select	NP_060017.1:p.Met188Ile
NR_037647.2:n.396G>C
NR_037648.2:n.741G>C