Canonical Allele Identifier: CA383229892

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126144839T>C (hg19) ; chr11:g.126274944T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274944T>C , CM000673.2:g.126274944T>C	GRCh38
NC_000011.9:g.126144839T>C , CM000673.1:g.126144839T>C	GRCh37
NC_000011.8:g.125650049T>C	NCBI36
NG_028029.1:g.10905T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.732T>C
ENST00000532101.6:n.734-383T>C
ENST00000532125.2:c.551T>C	ENSP00000434178.2:p.Val184Ala
ENST00000533839.6:c.86-850T>C	ENSP00000509952.1:n.86-850T>C
ENST00000534011.6:n.846T>C
ENST00000685484.1:c.554T>C	ENSP00000510622.1:p.Val185Ala
ENST00000685601.1:c.554T>C	ENSP00000510603.1:p.Val185Ala
ENST00000685765.1:c.554T>C	ENSP00000509991.1:p.Val185Ala
ENST00000685844.1:c.*169-383T>C	ENSP00000509820.1:n.*169-383T>C
ENST00000685857.1:n.988T>C
ENST00000686242.1:c.353T>C	ENSP00000508950.1:n.353T>C
ENST00000686888.1:c.*121T>C	ENSP00000509619.1:n.*121T>C
ENST00000687699.1:c.678T>C	ENSP00000508878.1:n.678T>C
ENST00000687786.1:n.2068-383T>C
ENST00000688100.1:n.1475T>C
ENST00000688588.1:c.554T>C	ENSP00000510802.1:p.Val185Ala
ENST00000688927.1:n.2460T>C
ENST00000689283.1:c.*217T>C	ENSP00000509050.1:n.*217T>C
ENST00000689477.1:c.*447T>C	ENSP00000508945.1:n.*447T>C
ENST00000689765.1:c.*169-427T>C	ENSP00000509625.1:n.*169-427T>C
ENST00000690512.1:c.*405T>C	ENSP00000509793.1:n.*405T>C
ENST00000692039.1:c.*352T>C	ENSP00000508821.1:n.*352T>C
ENST00000692336.1:c.578T>C	ENSP00000508540.1:p.Val193Ala
ENST00000693133.1:n.729T>C
ENST00000263578.10:c.554T>C MANE Select	ENSP00000263578.5:p.Val185Ala
ENST00000263578.9:c.554T>C	ENSP00000263578.5:p.Val185Ala
ENST00000524751.5:n.490T>C
ENST00000525083.5:n.352-383T>C
ENST00000525770.5:c.*186T>C	ENSP00000434739.1:n.*186T>C
ENST00000526366.5:n.485T>C
ENST00000527004.5:c.534-383T>C	ENSP00000436374.1:n.534-383T>C
ENST00000527875.1:n.384T>C
ENST00000530642.1:n.1031T>C
ENST00000532101.5:n.777T>C
ENST00000532125.1:c.512T>C	ENSP00000434178.1:p.Val171Ala
ENST00000533395.5:n.365-383T>C
ENST00000533839.5:n.238-850T>C
ENST00000534011.5:n.606T>C
ENST00000534315.5:n.944-383T>C
NM_017547.3:c.554T>C	NP_060017.1:p.Val185Ala
NR_037647.1:n.500T>C
NR_037648.1:n.740T>C
XM_006718879.2:c.44T>C	XP_006718942.1:p.Val15Ala
XM_006718880.2:c.-2-383T>C	XP_006718943.1:n.-2-383T>C
XM_006718881.2:c.-2-383T>C	XP_006718944.1:n.-2-383T>C
XM_011542895.1:c.44T>C	XP_011541197.1:p.Val15Ala
XM_011542896.1:c.44T>C	XP_011541198.1:p.Val15Ala
XM_006718879.3:c.44T>C	XP_006718942.1:p.Val15Ala
XM_006718881.3:c.-2-383T>C	XP_006718944.1:n.-2-383T>C
XM_011542895.2:c.44T>C	XP_011541197.1:p.Val15Ala
XM_011542896.2:c.44T>C	XP_011541198.1:p.Val15Ala
XM_017018000.2:c.554T>C	XP_016873489.1:p.Val185Ala
XM_017018001.1:c.44T>C	XP_016873490.1:p.Val15Ala
XM_017018002.1:c.44T>C	XP_016873491.1:p.Val15Ala
XM_017018003.2:c.-2-383T>C	XP_016873492.1:n.-2-383T>C
XM_017018004.1:c.-2-383T>C	XP_016873493.1:n.-2-383T>C
XM_017018005.1:c.-2-383T>C	XP_016873494.1:n.-2-383T>C
XM_017018006.2:c.-2-383T>C	XP_016873495.1:n.-2-383T>C
NM_017547.4:c.554T>C MANE Select	NP_060017.1:p.Val185Ala
NR_037647.2:n.386T>C
NR_037648.2:n.731T>C