Canonical Allele Identifier: CA477515133

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126144840T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274945T>C , CM000673.2:g.126274945T>C	GRCh38
NC_000011.9:g.126144840T>C , CM000673.1:g.126144840T>C	GRCh37
NC_000011.8:g.125650050T>C	NCBI36
NG_028029.1:g.10906T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.733T>C
ENST00000532101.6:n.734-382T>C
ENST00000532125.2:c.552T>C	ENSP00000434178.2:p.Val184=
ENST00000533839.6:c.86-849T>C	ENSP00000509952.1:n.86-849T>C
ENST00000534011.6:n.847T>C
ENST00000685484.1:c.555T>C	ENSP00000510622.1:p.Val185=
ENST00000685601.1:c.555T>C	ENSP00000510603.1:p.Val185=
ENST00000685765.1:c.555T>C	ENSP00000509991.1:p.Val185=
ENST00000685844.1:c.*169-382T>C	ENSP00000509820.1:n.*169-382T>C
ENST00000685857.1:n.989T>C
ENST00000686242.1:c.354T>C	ENSP00000508950.1:n.354T>C
ENST00000686888.1:c.*122T>C	ENSP00000509619.1:n.*122T>C
ENST00000687699.1:c.679T>C	ENSP00000508878.1:n.679T>C
ENST00000687786.1:n.2068-382T>C
ENST00000688100.1:n.1476T>C
ENST00000688588.1:c.555T>C	ENSP00000510802.1:p.Val185=
ENST00000688927.1:n.2461T>C
ENST00000689283.1:c.*218T>C	ENSP00000509050.1:n.*218T>C
ENST00000689477.1:c.*448T>C	ENSP00000508945.1:n.*448T>C
ENST00000689765.1:c.*169-426T>C	ENSP00000509625.1:n.*169-426T>C
ENST00000690512.1:c.*406T>C	ENSP00000509793.1:n.*406T>C
ENST00000692039.1:c.*353T>C	ENSP00000508821.1:n.*353T>C
ENST00000692336.1:c.579T>C	ENSP00000508540.1:p.Val193=
ENST00000693133.1:n.730T>C
ENST00000263578.10:c.555T>C MANE Select	ENSP00000263578.5:p.Val185=
ENST00000263578.9:c.555T>C	ENSP00000263578.5:p.Val185=
ENST00000524751.5:n.491T>C
ENST00000525083.5:n.352-382T>C
ENST00000525770.5:c.*187T>C	ENSP00000434739.1:n.*187T>C
ENST00000526366.5:n.486T>C
ENST00000527004.5:c.534-382T>C	ENSP00000436374.1:n.534-382T>C
ENST00000527875.1:n.385T>C
ENST00000530642.1:n.1032T>C
ENST00000532101.5:n.778T>C
ENST00000532125.1:c.513T>C	ENSP00000434178.1:p.Val171=
ENST00000533395.5:n.365-382T>C
ENST00000533839.5:n.238-849T>C
ENST00000534011.5:n.607T>C
ENST00000534315.5:n.944-382T>C
NM_017547.3:c.555T>C	NP_060017.1:p.Val185=
NR_037647.1:n.501T>C
NR_037648.1:n.741T>C
XM_006718879.2:c.45T>C	XP_006718942.1:p.Val15=
XM_006718880.2:c.-2-382T>C	XP_006718943.1:n.-2-382T>C
XM_006718881.2:c.-2-382T>C	XP_006718944.1:n.-2-382T>C
XM_011542895.1:c.45T>C	XP_011541197.1:p.Val15=
XM_011542896.1:c.45T>C	XP_011541198.1:p.Val15=
XM_006718879.3:c.45T>C	XP_006718942.1:p.Val15=
XM_006718881.3:c.-2-382T>C	XP_006718944.1:n.-2-382T>C
XM_011542895.2:c.45T>C	XP_011541197.1:p.Val15=
XM_011542896.2:c.45T>C	XP_011541198.1:p.Val15=
XM_017018000.2:c.555T>C	XP_016873489.1:p.Val185=
XM_017018001.1:c.45T>C	XP_016873490.1:p.Val15=
XM_017018002.1:c.45T>C	XP_016873491.1:p.Val15=
XM_017018003.2:c.-2-382T>C	XP_016873492.1:n.-2-382T>C
XM_017018004.1:c.-2-382T>C	XP_016873493.1:n.-2-382T>C
XM_017018005.1:c.-2-382T>C	XP_016873494.1:n.-2-382T>C
XM_017018006.2:c.-2-382T>C	XP_016873495.1:n.-2-382T>C
NM_017547.4:c.555T>C MANE Select	NP_060017.1:p.Val185=
NR_037647.2:n.387T>C
NR_037648.2:n.732T>C