Canonical Allele Identifier: CA383230161

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145261T>C (hg19) ; chr11:g.126275366T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275366T>C , CM000673.2:g.126275366T>C	GRCh38
NC_000011.9:g.126145261T>C , CM000673.1:g.126145261T>C	GRCh37
NC_000011.8:g.125650471T>C	NCBI36
NG_028029.1:g.11327T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1154T>C
ENST00000532101.6:n.773T>C
ENST00000532125.2:c.668T>C	ENSP00000434178.2:p.Leu223Pro
ENST00000533839.6:c.86-428T>C	ENSP00000509952.1:n.86-428T>C
ENST00000534011.6:n.963T>C
ENST00000685484.1:c.671T>C	ENSP00000510622.1:p.Leu224Pro
ENST00000685601.1:c.671T>C	ENSP00000510603.1:p.Leu224Pro
ENST00000685765.1:c.671T>C	ENSP00000509991.1:p.Leu224Pro
ENST00000685844.1:c.*208T>C	ENSP00000509820.1:n.*208T>C
ENST00000685857.1:n.1410T>C
ENST00000686242.1:c.470T>C	ENSP00000508950.1:n.470T>C
ENST00000686888.1:c.*238T>C	ENSP00000509619.1:n.*238T>C
ENST00000687699.1:c.795T>C	ENSP00000508878.1:n.795T>C
ENST00000687786.1:n.2107T>C
ENST00000688100.1:n.1592T>C
ENST00000688588.1:c.671T>C	ENSP00000510802.1:p.Leu224Pro
ENST00000688927.1:n.2882T>C
ENST00000689283.1:c.*334T>C	ENSP00000509050.1:n.*334T>C
ENST00000689477.1:c.*564T>C	ENSP00000508945.1:n.*564T>C
ENST00000689765.1:c.*169-5T>C	ENSP00000509625.1:n.*169-5T>C
ENST00000690512.1:c.*522T>C	ENSP00000509793.1:n.*522T>C
ENST00000692039.1:c.*469T>C	ENSP00000508821.1:n.*469T>C
ENST00000692336.1:c.695T>C	ENSP00000508540.1:p.Leu232Pro
ENST00000693133.1:n.1151T>C
ENST00000263578.10:c.671T>C MANE Select	ENSP00000263578.5:p.Leu224Pro
ENST00000263578.9:c.671T>C	ENSP00000263578.5:p.Leu224Pro
ENST00000525083.5:n.391T>C
ENST00000525770.5:c.*303T>C	ENSP00000434739.1:n.*303T>C
ENST00000527004.5:c.*15T>C	ENSP00000436374.1:n.*15T>C
ENST00000530642.1:n.1453T>C
ENST00000532101.5:n.894T>C
ENST00000532125.1:c.629T>C	ENSP00000434178.1:p.Leu210Pro
ENST00000533395.5:n.404T>C
ENST00000533839.5:n.238-428T>C
ENST00000534011.5:n.723T>C
ENST00000534315.5:n.983T>C
NM_017547.3:c.671T>C	NP_060017.1:p.Leu224Pro
NR_037647.1:n.617T>C
NR_037648.1:n.857T>C
XM_006718879.2:c.161T>C	XP_006718942.1:p.Leu54Pro
XM_006718880.2:c.38T>C	XP_006718943.1:p.Leu13Pro
XM_006718881.2:c.38T>C	XP_006718944.1:p.Leu13Pro
XM_011542895.1:c.161T>C	XP_011541197.1:p.Leu54Pro
XM_011542896.1:c.161T>C	XP_011541198.1:p.Leu54Pro
XM_006718879.3:c.161T>C	XP_006718942.1:p.Leu54Pro
XM_006718881.3:c.38T>C	XP_006718944.1:p.Leu13Pro
XM_011542895.2:c.161T>C	XP_011541197.1:p.Leu54Pro
XM_011542896.2:c.161T>C	XP_011541198.1:p.Leu54Pro
XM_017018000.2:c.671T>C	XP_016873489.1:p.Leu224Pro
XM_017018001.1:c.161T>C	XP_016873490.1:p.Leu54Pro
XM_017018002.1:c.161T>C	XP_016873491.1:p.Leu54Pro
XM_017018003.2:c.38T>C	XP_016873492.1:p.Leu13Pro
XM_017018004.1:c.38T>C	XP_016873493.1:p.Leu13Pro
XM_017018005.1:c.38T>C	XP_016873494.1:p.Leu13Pro
XM_017018006.2:c.38T>C	XP_016873495.1:p.Leu13Pro
NM_017547.4:c.671T>C MANE Select	NP_060017.1:p.Leu224Pro
NR_037647.2:n.503T>C
NR_037648.2:n.848T>C