Canonical Allele Identifier: CA383230102

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145235A>T (hg19) ; chr11:g.126275340A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275340A>T , CM000673.2:g.126275340A>T	GRCh38
NC_000011.9:g.126145235A>T , CM000673.1:g.126145235A>T	GRCh37
NC_000011.8:g.125650445A>T	NCBI36
NG_028029.1:g.11301A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1128A>T
ENST00000532101.6:n.747A>T
ENST00000532125.2:c.642A>T	ENSP00000434178.2:p.Glu214Asp
ENST00000533839.6:c.86-454A>T	ENSP00000509952.1:n.86-454A>T
ENST00000534011.6:n.937A>T
ENST00000685484.1:c.645A>T	ENSP00000510622.1:p.Glu215Asp
ENST00000685601.1:c.645A>T	ENSP00000510603.1:p.Glu215Asp
ENST00000685765.1:c.645A>T	ENSP00000509991.1:p.Glu215Asp
ENST00000685844.1:c.*182A>T	ENSP00000509820.1:n.*182A>T
ENST00000685857.1:n.1384A>T
ENST00000686242.1:c.444A>T	ENSP00000508950.1:n.444A>T
ENST00000686888.1:c.*212A>T	ENSP00000509619.1:n.*212A>T
ENST00000687699.1:c.769A>T	ENSP00000508878.1:n.769A>T
ENST00000687786.1:n.2081A>T
ENST00000688100.1:n.1566A>T
ENST00000688588.1:c.645A>T	ENSP00000510802.1:p.Glu215Asp
ENST00000688927.1:n.2856A>T
ENST00000689283.1:c.*308A>T	ENSP00000509050.1:n.*308A>T
ENST00000689477.1:c.*538A>T	ENSP00000508945.1:n.*538A>T
ENST00000689765.1:c.*169-31A>T	ENSP00000509625.1:n.*169-31A>T
ENST00000690512.1:c.*496A>T	ENSP00000509793.1:n.*496A>T
ENST00000692039.1:c.*443A>T	ENSP00000508821.1:n.*443A>T
ENST00000692336.1:c.669A>T	ENSP00000508540.1:p.Glu223Asp
ENST00000693133.1:n.1125A>T
ENST00000263578.10:c.645A>T MANE Select	ENSP00000263578.5:p.Glu215Asp
ENST00000263578.9:c.645A>T	ENSP00000263578.5:p.Glu215Asp
ENST00000524751.5:n.886A>T
ENST00000525083.5:n.365A>T
ENST00000525770.5:c.*277A>T	ENSP00000434739.1:n.*277A>T
ENST00000527004.5:c.547A>T	ENSP00000436374.1:p.Arg183Trp
ENST00000530642.1:n.1427A>T
ENST00000532101.5:n.868A>T
ENST00000532125.1:c.603A>T	ENSP00000434178.1:p.Glu201Asp
ENST00000533395.5:n.378A>T
ENST00000533839.5:n.238-454A>T
ENST00000534011.5:n.697A>T
ENST00000534315.5:n.957A>T
NM_017547.3:c.645A>T	NP_060017.1:p.Glu215Asp
NR_037647.1:n.591A>T
NR_037648.1:n.831A>T
XM_006718879.2:c.135A>T	XP_006718942.1:p.Glu45Asp
XM_006718880.2:c.12A>T	XP_006718943.1:p.Glu4Asp
XM_006718881.2:c.12A>T	XP_006718944.1:p.Glu4Asp
XM_011542895.1:c.135A>T	XP_011541197.1:p.Glu45Asp
XM_011542896.1:c.135A>T	XP_011541198.1:p.Glu45Asp
XM_006718879.3:c.135A>T	XP_006718942.1:p.Glu45Asp
XM_006718881.3:c.12A>T	XP_006718944.1:p.Glu4Asp
XM_011542895.2:c.135A>T	XP_011541197.1:p.Glu45Asp
XM_011542896.2:c.135A>T	XP_011541198.1:p.Glu45Asp
XM_017018000.2:c.645A>T	XP_016873489.1:p.Glu215Asp
XM_017018001.1:c.135A>T	XP_016873490.1:p.Glu45Asp
XM_017018002.1:c.135A>T	XP_016873491.1:p.Glu45Asp
XM_017018003.2:c.12A>T	XP_016873492.1:p.Glu4Asp
XM_017018004.1:c.12A>T	XP_016873493.1:p.Glu4Asp
XM_017018005.1:c.12A>T	XP_016873494.1:p.Glu4Asp
XM_017018006.2:c.12A>T	XP_016873495.1:p.Glu4Asp
NM_017547.4:c.645A>T MANE Select	NP_060017.1:p.Glu215Asp
NR_037647.2:n.477A>T
NR_037648.2:n.822A>T