Canonical Allele Identifier: CA383230074

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145225T>A (hg19) ; chr11:g.126275330T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275330T>A , CM000673.2:g.126275330T>A	GRCh38
NC_000011.9:g.126145225T>A , CM000673.1:g.126145225T>A	GRCh37
NC_000011.8:g.125650435T>A	NCBI36
NG_028029.1:g.11291T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1118T>A
ENST00000532101.6:n.737T>A
ENST00000532125.2:c.632T>A	ENSP00000434178.2:p.Met211Lys
ENST00000533839.6:c.86-464T>A	ENSP00000509952.1:n.86-464T>A
ENST00000534011.6:n.927T>A
ENST00000685484.1:c.635T>A	ENSP00000510622.1:p.Met212Lys
ENST00000685601.1:c.635T>A	ENSP00000510603.1:p.Met212Lys
ENST00000685765.1:c.635T>A	ENSP00000509991.1:p.Met212Lys
ENST00000685844.1:c.*172T>A	ENSP00000509820.1:n.*172T>A
ENST00000685857.1:n.1374T>A
ENST00000686242.1:c.434T>A	ENSP00000508950.1:n.434T>A
ENST00000686888.1:c.*202T>A	ENSP00000509619.1:n.*202T>A
ENST00000687699.1:c.759T>A	ENSP00000508878.1:n.759T>A
ENST00000687786.1:n.2071T>A
ENST00000688100.1:n.1556T>A
ENST00000688588.1:c.635T>A	ENSP00000510802.1:p.Met212Lys
ENST00000688927.1:n.2846T>A
ENST00000689283.1:c.*298T>A	ENSP00000509050.1:n.*298T>A
ENST00000689477.1:c.*528T>A	ENSP00000508945.1:n.*528T>A
ENST00000689765.1:c.*169-41T>A	ENSP00000509625.1:n.*169-41T>A
ENST00000690512.1:c.*486T>A	ENSP00000509793.1:n.*486T>A
ENST00000692039.1:c.*433T>A	ENSP00000508821.1:n.*433T>A
ENST00000692336.1:c.659T>A	ENSP00000508540.1:p.Met220Lys
ENST00000693133.1:n.1115T>A
ENST00000263578.10:c.635T>A MANE Select	ENSP00000263578.5:p.Met212Lys
ENST00000263578.9:c.635T>A	ENSP00000263578.5:p.Met212Lys
ENST00000524751.5:n.876T>A
ENST00000525083.5:n.355T>A
ENST00000525770.5:c.*267T>A	ENSP00000434739.1:n.*267T>A
ENST00000527004.5:c.537T>A	ENSP00000436374.1:p.Asp179Glu
ENST00000530642.1:n.1417T>A
ENST00000532101.5:n.858T>A
ENST00000532125.1:c.593T>A	ENSP00000434178.1:p.Met198Lys
ENST00000533395.5:n.368T>A
ENST00000533839.5:n.238-464T>A
ENST00000534011.5:n.687T>A
ENST00000534315.5:n.947T>A
NM_017547.3:c.635T>A	NP_060017.1:p.Met212Lys
NR_037647.1:n.581T>A
NR_037648.1:n.821T>A
XM_006718879.2:c.125T>A	XP_006718942.1:p.Met42Lys
XM_006718880.2:c.2T>A	XP_006718943.1:p.Met1Lys
XM_006718881.2:c.2T>A	XP_006718944.1:p.Met1Lys
XM_011542895.1:c.125T>A	XP_011541197.1:p.Met42Lys
XM_011542896.1:c.125T>A	XP_011541198.1:p.Met42Lys
XM_006718879.3:c.125T>A	XP_006718942.1:p.Met42Lys
XM_006718881.3:c.2T>A	XP_006718944.1:p.Met1Lys
XM_011542895.2:c.125T>A	XP_011541197.1:p.Met42Lys
XM_011542896.2:c.125T>A	XP_011541198.1:p.Met42Lys
XM_017018000.2:c.635T>A	XP_016873489.1:p.Met212Lys
XM_017018001.1:c.125T>A	XP_016873490.1:p.Met42Lys
XM_017018002.1:c.125T>A	XP_016873491.1:p.Met42Lys
XM_017018003.2:c.2T>A	XP_016873492.1:p.Met1Lys
XM_017018004.1:c.2T>A	XP_016873493.1:p.Met1Lys
XM_017018005.1:c.2T>A	XP_016873494.1:p.Met1Lys
XM_017018006.2:c.2T>A	XP_016873495.1:p.Met1Lys
NM_017547.4:c.635T>A MANE Select	NP_060017.1:p.Met212Lys
NR_037647.2:n.467T>A
NR_037648.2:n.812T>A