Canonical Allele Identifier: CA2559123955
Gene: NR4A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156325810_156325813del , CM000664.2:g.156325810_156325813del GRCh38
NC_000002.11:g.157182322_157182325del , CM000664.1:g.157182322_157182325del GRCh37
NC_000002.10:g.156890568_156890571del NCBI36
NG_011821.1:g.11963_11966del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700228.1:c.1524_1527del ENSP00000514865.1:p.Lys509TrpfsTer10
ENST00000700229.1:c.692_695del
ENST00000700230.1:c.1268_1271del ENSP00000514867.1:n.1268_1271del
ENST00000700231.1:c.1653_1656del ENSP00000514868.1:p.Lys552TrpfsTer10
ENST00000339562.9:c.1728_1731del MANE Select ENSP00000344479.4:p.Lys577TrpfsTer10
ENST00000675870.1:c.*239_*242del ENSP00000502739.1:n.*239_*242del
ENST00000339562.8:c.1728_1731del ENSP00000344479.4:p.Lys577TrpfsTer10
ENST00000409108.6:c.1624_1627del ENSP00000386993.2:p.Glu542LeufsTer22
ENST00000409572.5:c.1728_1731del ENSP00000386747.1:p.Lys577TrpfsTer10
ENST00000417764.5:c.*239_*242del ENSP00000415632.1:n.*239_*242del
ENST00000417972.5:c.*239_*242del ENSP00000394671.1:n.*239_*242del
ENST00000426264.5:c.1539_1542del ENSP00000389986.1:p.Lys514TrpfsTer10
ENST00000429376.5:c.1435_1438del ENSP00000410952.1:p.Glu479LeufsTer22
NM_006186.3:c.1728_1731del NP_006177.1:p.Lys577TrpfsTer10
XM_005246621.2:c.1761_1764del XP_005246678.1:p.Lys588TrpfsTer10
XM_005246622.2:c.1539_1542del XP_005246679.1:p.Lys514TrpfsTer10
XM_005246623.1:c.1539_1542del XP_005246680.1:p.Lys514TrpfsTer10
XM_006712553.2:c.1686_1689del XP_006712616.1:p.Lys563TrpfsTer10
XM_011511246.1:c.1657_1660del XP_011509548.1:p.Glu553LeufsTer22
NM_173173.2:c.1539_1542del NP_775265.1:p.Lys514TrpfsTer10
XM_005246621.4:c.1761_1764del XP_005246678.1:p.Lys588TrpfsTer10
XM_006712553.4:c.1686_1689del XP_006712616.1:p.Lys563TrpfsTer10
XM_011511246.2:c.1657_1660del XP_011509548.1:p.Glu553LeufsTer22
XM_017004219.2:c.1728_1731del XP_016859708.1:p.Lys577TrpfsTer10
XM_017004220.2:c.1653_1656del XP_016859709.1:p.Lys552TrpfsTer10
XR_001738751.2:n.1975_1978del
XR_001738752.2:n.1797_1800del
XR_427087.4:n.1854_1857del
NM_006186.4:c.1728_1731del MANE Select NP_006177.1:p.Lys577TrpfsTer10
NM_173173.3:c.1539_1542del NP_775265.1:p.Lys514TrpfsTer10