Canonical Allele Identifier: CA2661538852
Gene: NR4A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156325844del , CM000664.2:g.156325844del GRCh38
NC_000002.11:g.157182356del , CM000664.1:g.157182356del GRCh37
NC_000002.10:g.156890602del NCBI36
NG_011821.1:g.11932del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700228.1:c.1493del ENSP00000514865.1:p.Cys498SerfsTer11
ENST00000700229.1:c.661del
ENST00000700230.1:c.1237del ENSP00000514867.1:n.1237del
ENST00000700231.1:c.1622del ENSP00000514868.1:p.Cys541SerfsTer11
ENST00000339562.9:c.1697del MANE Select ENSP00000344479.4:p.Cys566SerfsTer11
ENST00000675870.1:c.*208del ENSP00000502739.1:n.*208del
ENST00000339562.8:c.1697del ENSP00000344479.4:p.Cys566SerfsTer11
ENST00000409108.6:c.1593del ENSP00000386993.2:p.Leu531PhefsTer?
ENST00000409572.5:c.1697del ENSP00000386747.1:p.Cys566SerfsTer11
ENST00000417764.5:c.*208del ENSP00000415632.1:n.*208del
ENST00000417972.5:c.*208del ENSP00000394671.1:n.*208del
ENST00000426264.5:c.1508del ENSP00000389986.1:p.Cys503SerfsTer11
ENST00000429376.5:c.1404del ENSP00000410952.1:p.Leu468PhefsTer?
NM_006186.3:c.1697del NP_006177.1:p.Cys566SerfsTer11
XM_005246621.2:c.1730del XP_005246678.1:p.Cys577SerfsTer11
XM_005246622.2:c.1508del XP_005246679.1:p.Cys503SerfsTer11
XM_005246623.1:c.1508del XP_005246680.1:p.Cys503SerfsTer11
XM_006712553.2:c.1655del XP_006712616.1:p.Cys552SerfsTer11
XM_011511246.1:c.1626del XP_011509548.1:p.Leu542PhefsTer?
NM_173173.2:c.1508del NP_775265.1:p.Cys503SerfsTer11
XM_005246621.4:c.1730del XP_005246678.1:p.Cys577SerfsTer11
XM_006712553.4:c.1655del XP_006712616.1:p.Cys552SerfsTer11
XM_011511246.2:c.1626del XP_011509548.1:p.Leu542PhefsTer?
XM_017004219.2:c.1697del XP_016859708.1:p.Cys566SerfsTer11
XM_017004220.2:c.1622del XP_016859709.1:p.Cys541SerfsTer11
XR_001738751.2:n.1944del
XR_001738752.2:n.1766del
XR_427087.4:n.1823del
NM_006186.4:c.1697del MANE Select NP_006177.1:p.Cys566SerfsTer11
NM_173173.3:c.1508del NP_775265.1:p.Cys503SerfsTer11