Canonical Allele Identifier: CA2661538794
Gene: NR4A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156325620_156325635del , CM000664.2:g.156325620_156325635del GRCh38
NC_000002.11:g.157182132_157182147del , CM000664.1:g.157182132_157182147del GRCh37
NC_000002.10:g.156890378_156890393del NCBI36
NG_011821.1:g.12144_12159del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700228.1:c.*112_*127del ENSP00000514865.1:n.*112_*127del
ENST00000700229.1:c.873_888del
ENST00000700230.1:c.1449_1464del ENSP00000514867.1:n.1449_1464del
ENST00000700231.1:c.*112_*127del ENSP00000514868.1:n.*112_*127del
ENST00000339562.9:c.*112_*127del MANE Select ENSP00000344479.4:n.*112_*127del
ENST00000675870.1:c.*420_*435del ENSP00000502739.1:n.*420_*435del
ENST00000339562.8:c.*112_*127del ENSP00000344479.4:n.*112_*127del
ENST00000409572.5:c.*112_*127del ENSP00000386747.1:n.*112_*127del
ENST00000417764.5:c.*420_*435del ENSP00000415632.1:n.*420_*435del
ENST00000417972.5:c.*420_*435del ENSP00000394671.1:n.*420_*435del
ENST00000426264.5:c.*112_*127del ENSP00000389986.1:n.*112_*127del
NM_006186.3:c.*112_*127del NP_006177.1:n.*112_*127del
XM_005246621.2:c.*112_*127del XP_005246678.1:n.*112_*127del
XM_005246622.2:c.*112_*127del XP_005246679.1:n.*112_*127del
XM_005246623.1:c.*112_*127del XP_005246680.1:n.*112_*127del
XM_006712553.2:c.*112_*127del XP_006712616.1:n.*112_*127del
XM_011511246.1:c.*143_*158del XP_011509548.1:n.*143_*158del
NM_173173.2:c.*112_*127del NP_775265.1:n.*112_*127del
XM_005246621.4:c.*112_*127del XP_005246678.1:n.*112_*127del
XM_006712553.4:c.*112_*127del XP_006712616.1:n.*112_*127del
XM_011511246.2:c.*143_*158del XP_011509548.1:n.*143_*158del
XM_017004219.2:c.*112_*127del XP_016859708.1:n.*112_*127del
XM_017004220.2:c.*112_*127del XP_016859709.1:n.*112_*127del
XR_001738751.2:n.2156_2171del
XR_001738752.2:n.1978_1993del
XR_427087.4:n.2035_2050del
NM_006186.4:c.*112_*127del MANE Select NP_006177.1:n.*112_*127del
NM_173173.3:c.*112_*127del NP_775265.1:n.*112_*127del