Canonical Allele Identifier: CA477515969

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145238T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275343T>G , CM000673.2:g.126275343T>G	GRCh38
NC_000011.9:g.126145238T>G , CM000673.1:g.126145238T>G	GRCh37
NC_000011.8:g.125650448T>G	NCBI36
NG_028029.1:g.11304T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1131T>G
ENST00000532101.6:n.750T>G
ENST00000532125.2:c.645T>G	ENSP00000434178.2:p.Gly215=
ENST00000533839.6:c.86-451T>G	ENSP00000509952.1:n.86-451T>G
ENST00000534011.6:n.940T>G
ENST00000685484.1:c.648T>G	ENSP00000510622.1:p.Gly216=
ENST00000685601.1:c.648T>G	ENSP00000510603.1:p.Gly216=
ENST00000685765.1:c.648T>G	ENSP00000509991.1:p.Gly216=
ENST00000685844.1:c.*185T>G	ENSP00000509820.1:n.*185T>G
ENST00000685857.1:n.1387T>G
ENST00000686242.1:c.447T>G	ENSP00000508950.1:n.447T>G
ENST00000686888.1:c.*215T>G	ENSP00000509619.1:n.*215T>G
ENST00000687699.1:c.772T>G	ENSP00000508878.1:n.772T>G
ENST00000687786.1:n.2084T>G
ENST00000688100.1:n.1569T>G
ENST00000688588.1:c.648T>G	ENSP00000510802.1:p.Gly216=
ENST00000688927.1:n.2859T>G
ENST00000689283.1:c.*311T>G	ENSP00000509050.1:n.*311T>G
ENST00000689477.1:c.*541T>G	ENSP00000508945.1:n.*541T>G
ENST00000689765.1:c.*169-28T>G	ENSP00000509625.1:n.*169-28T>G
ENST00000690512.1:c.*499T>G	ENSP00000509793.1:n.*499T>G
ENST00000692039.1:c.*446T>G	ENSP00000508821.1:n.*446T>G
ENST00000692336.1:c.672T>G	ENSP00000508540.1:p.Gly224=
ENST00000693133.1:n.1128T>G
ENST00000263578.10:c.648T>G MANE Select	ENSP00000263578.5:p.Gly216=
ENST00000263578.9:c.648T>G	ENSP00000263578.5:p.Gly216=
ENST00000524751.5:n.889T>G
ENST00000525083.5:n.368T>G
ENST00000525770.5:c.*280T>G	ENSP00000434739.1:n.*280T>G
ENST00000527004.5:c.550T>G	ENSP00000436374.1:p.Leu184Val
ENST00000530642.1:n.1430T>G
ENST00000532101.5:n.871T>G
ENST00000532125.1:c.606T>G	ENSP00000434178.1:p.Gly202=
ENST00000533395.5:n.381T>G
ENST00000533839.5:n.238-451T>G
ENST00000534011.5:n.700T>G
ENST00000534315.5:n.960T>G
NM_017547.3:c.648T>G	NP_060017.1:p.Gly216=
NR_037647.1:n.594T>G
NR_037648.1:n.834T>G
XM_006718879.2:c.138T>G	XP_006718942.1:p.Gly46=
XM_006718880.2:c.15T>G	XP_006718943.1:p.Gly5=
XM_006718881.2:c.15T>G	XP_006718944.1:p.Gly5=
XM_011542895.1:c.138T>G	XP_011541197.1:p.Gly46=
XM_011542896.1:c.138T>G	XP_011541198.1:p.Gly46=
XM_006718879.3:c.138T>G	XP_006718942.1:p.Gly46=
XM_006718881.3:c.15T>G	XP_006718944.1:p.Gly5=
XM_011542895.2:c.138T>G	XP_011541197.1:p.Gly46=
XM_011542896.2:c.138T>G	XP_011541198.1:p.Gly46=
XM_017018000.2:c.648T>G	XP_016873489.1:p.Gly216=
XM_017018001.1:c.138T>G	XP_016873490.1:p.Gly46=
XM_017018002.1:c.138T>G	XP_016873491.1:p.Gly46=
XM_017018003.2:c.15T>G	XP_016873492.1:p.Gly5=
XM_017018004.1:c.15T>G	XP_016873493.1:p.Gly5=
XM_017018005.1:c.15T>G	XP_016873494.1:p.Gly5=
XM_017018006.2:c.15T>G	XP_016873495.1:p.Gly5=
NM_017547.4:c.648T>G MANE Select	NP_060017.1:p.Gly216=
NR_037647.2:n.480T>G
NR_037648.2:n.825T>G