Canonical Allele Identifier: CA383230084

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145228A>C (hg19) ; chr11:g.126275333A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275333A>C , CM000673.2:g.126275333A>C	GRCh38
NC_000011.9:g.126145228A>C , CM000673.1:g.126145228A>C	GRCh37
NC_000011.8:g.125650438A>C	NCBI36
NG_028029.1:g.11294A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1121A>C
ENST00000532101.6:n.740A>C
ENST00000532125.2:c.635A>C	ENSP00000434178.2:p.Glu212Ala
ENST00000533839.6:c.86-461A>C	ENSP00000509952.1:n.86-461A>C
ENST00000534011.6:n.930A>C
ENST00000685484.1:c.638A>C	ENSP00000510622.1:p.Glu213Ala
ENST00000685601.1:c.638A>C	ENSP00000510603.1:p.Glu213Ala
ENST00000685765.1:c.638A>C	ENSP00000509991.1:p.Glu213Ala
ENST00000685844.1:c.*175A>C	ENSP00000509820.1:n.*175A>C
ENST00000685857.1:n.1377A>C
ENST00000686242.1:c.437A>C	ENSP00000508950.1:n.437A>C
ENST00000686888.1:c.*205A>C	ENSP00000509619.1:n.*205A>C
ENST00000687699.1:c.762A>C	ENSP00000508878.1:n.762A>C
ENST00000687786.1:n.2074A>C
ENST00000688100.1:n.1559A>C
ENST00000688588.1:c.638A>C	ENSP00000510802.1:p.Glu213Ala
ENST00000688927.1:n.2849A>C
ENST00000689283.1:c.*301A>C	ENSP00000509050.1:n.*301A>C
ENST00000689477.1:c.*531A>C	ENSP00000508945.1:n.*531A>C
ENST00000689765.1:c.*169-38A>C	ENSP00000509625.1:n.*169-38A>C
ENST00000690512.1:c.*489A>C	ENSP00000509793.1:n.*489A>C
ENST00000692039.1:c.*436A>C	ENSP00000508821.1:n.*436A>C
ENST00000692336.1:c.662A>C	ENSP00000508540.1:p.Glu221Ala
ENST00000693133.1:n.1118A>C
ENST00000263578.10:c.638A>C MANE Select	ENSP00000263578.5:p.Glu213Ala
ENST00000263578.9:c.638A>C	ENSP00000263578.5:p.Glu213Ala
ENST00000524751.5:n.879A>C
ENST00000525083.5:n.358A>C
ENST00000525770.5:c.*270A>C	ENSP00000434739.1:n.*270A>C
ENST00000527004.5:c.540A>C	ENSP00000436374.1:p.Gly180=
ENST00000530642.1:n.1420A>C
ENST00000532101.5:n.861A>C
ENST00000532125.1:c.596A>C	ENSP00000434178.1:p.Glu199Ala
ENST00000533395.5:n.371A>C
ENST00000533839.5:n.238-461A>C
ENST00000534011.5:n.690A>C
ENST00000534315.5:n.950A>C
NM_017547.3:c.638A>C	NP_060017.1:p.Glu213Ala
NR_037647.1:n.584A>C
NR_037648.1:n.824A>C
XM_006718879.2:c.128A>C	XP_006718942.1:p.Glu43Ala
XM_006718880.2:c.5A>C	XP_006718943.1:p.Glu2Ala
XM_006718881.2:c.5A>C	XP_006718944.1:p.Glu2Ala
XM_011542895.1:c.128A>C	XP_011541197.1:p.Glu43Ala
XM_011542896.1:c.128A>C	XP_011541198.1:p.Glu43Ala
XM_006718879.3:c.128A>C	XP_006718942.1:p.Glu43Ala
XM_006718881.3:c.5A>C	XP_006718944.1:p.Glu2Ala
XM_011542895.2:c.128A>C	XP_011541197.1:p.Glu43Ala
XM_011542896.2:c.128A>C	XP_011541198.1:p.Glu43Ala
XM_017018000.2:c.638A>C	XP_016873489.1:p.Glu213Ala
XM_017018001.1:c.128A>C	XP_016873490.1:p.Glu43Ala
XM_017018002.1:c.128A>C	XP_016873491.1:p.Glu43Ala
XM_017018003.2:c.5A>C	XP_016873492.1:p.Glu2Ala
XM_017018004.1:c.5A>C	XP_016873493.1:p.Glu2Ala
XM_017018005.1:c.5A>C	XP_016873494.1:p.Glu2Ala
XM_017018006.2:c.5A>C	XP_016873495.1:p.Glu2Ala
NM_017547.4:c.638A>C MANE Select	NP_060017.1:p.Glu213Ala
NR_037647.2:n.470A>C
NR_037648.2:n.815A>C