Canonical Allele Identifier: CA383230079

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145226G>T (hg19) ; chr11:g.126275331G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275331G>T , CM000673.2:g.126275331G>T	GRCh38
NC_000011.9:g.126145226G>T , CM000673.1:g.126145226G>T	GRCh37
NC_000011.8:g.125650436G>T	NCBI36
NG_028029.1:g.11292G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1119G>T
ENST00000532101.6:n.738G>T
ENST00000532125.2:c.633G>T	ENSP00000434178.2:p.Met211Ile
ENST00000533839.6:c.86-463G>T	ENSP00000509952.1:n.86-463G>T
ENST00000534011.6:n.928G>T
ENST00000685484.1:c.636G>T	ENSP00000510622.1:p.Met212Ile
ENST00000685601.1:c.636G>T	ENSP00000510603.1:p.Met212Ile
ENST00000685765.1:c.636G>T	ENSP00000509991.1:p.Met212Ile
ENST00000685844.1:c.*173G>T	ENSP00000509820.1:n.*173G>T
ENST00000685857.1:n.1375G>T
ENST00000686242.1:c.435G>T	ENSP00000508950.1:n.435G>T
ENST00000686888.1:c.*203G>T	ENSP00000509619.1:n.*203G>T
ENST00000687699.1:c.760G>T	ENSP00000508878.1:n.760G>T
ENST00000687786.1:n.2072G>T
ENST00000688100.1:n.1557G>T
ENST00000688588.1:c.636G>T	ENSP00000510802.1:p.Met212Ile
ENST00000688927.1:n.2847G>T
ENST00000689283.1:c.*299G>T	ENSP00000509050.1:n.*299G>T
ENST00000689477.1:c.*529G>T	ENSP00000508945.1:n.*529G>T
ENST00000689765.1:c.*169-40G>T	ENSP00000509625.1:n.*169-40G>T
ENST00000690512.1:c.*487G>T	ENSP00000509793.1:n.*487G>T
ENST00000692039.1:c.*434G>T	ENSP00000508821.1:n.*434G>T
ENST00000692336.1:c.660G>T	ENSP00000508540.1:p.Met220Ile
ENST00000693133.1:n.1116G>T
ENST00000263578.10:c.636G>T MANE Select	ENSP00000263578.5:p.Met212Ile
ENST00000263578.9:c.636G>T	ENSP00000263578.5:p.Met212Ile
ENST00000524751.5:n.877G>T
ENST00000525083.5:n.356G>T
ENST00000525770.5:c.*268G>T	ENSP00000434739.1:n.*268G>T
ENST00000527004.5:c.538G>T	ENSP00000436374.1:p.Gly180Ter
ENST00000530642.1:n.1418G>T
ENST00000532101.5:n.859G>T
ENST00000532125.1:c.594G>T	ENSP00000434178.1:p.Met198Ile
ENST00000533395.5:n.369G>T
ENST00000533839.5:n.238-463G>T
ENST00000534011.5:n.688G>T
ENST00000534315.5:n.948G>T
NM_017547.3:c.636G>T	NP_060017.1:p.Met212Ile
NR_037647.1:n.582G>T
NR_037648.1:n.822G>T
XM_006718879.2:c.126G>T	XP_006718942.1:p.Met42Ile
XM_006718880.2:c.3G>T	XP_006718943.1:p.Met1Ile
XM_006718881.2:c.3G>T	XP_006718944.1:p.Met1Ile
XM_011542895.1:c.126G>T	XP_011541197.1:p.Met42Ile
XM_011542896.1:c.126G>T	XP_011541198.1:p.Met42Ile
XM_006718879.3:c.126G>T	XP_006718942.1:p.Met42Ile
XM_006718881.3:c.3G>T	XP_006718944.1:p.Met1Ile
XM_011542895.2:c.126G>T	XP_011541197.1:p.Met42Ile
XM_011542896.2:c.126G>T	XP_011541198.1:p.Met42Ile
XM_017018000.2:c.636G>T	XP_016873489.1:p.Met212Ile
XM_017018001.1:c.126G>T	XP_016873490.1:p.Met42Ile
XM_017018002.1:c.126G>T	XP_016873491.1:p.Met42Ile
XM_017018003.2:c.3G>T	XP_016873492.1:p.Met1Ile
XM_017018004.1:c.3G>T	XP_016873493.1:p.Met1Ile
XM_017018005.1:c.3G>T	XP_016873494.1:p.Met1Ile
XM_017018006.2:c.3G>T	XP_016873495.1:p.Met1Ile
NM_017547.4:c.636G>T MANE Select	NP_060017.1:p.Met212Ile
NR_037647.2:n.468G>T
NR_037648.2:n.813G>T