Canonical Allele Identifier: CA1300458826
Gene: NR4A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156325652_156325661delinsTGCTCACACG , CM000664.2:g.156325652_156325661delinsTGCTCACACG GRCh38
NC_000002.11:g.157182164_157182173delinsTGCTCACACG , CM000664.1:g.157182164_157182173delinsTGCTCACACG GRCh37
NC_000002.10:g.156890410_156890419delinsTGCTCACACG NCBI36
NG_011821.1:g.12115_12124delinsCGTGTGAGCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700228.1:c.*83_*92delinsCGTGTGAGCA ENSP00000514865.1:n.*83_*92delinsCGTGTGAGCA
ENST00000700229.1:c.844_853delinsCGTGTGAGCA
ENST00000700230.1:c.1420_1429delinsCGTGTGAGCA ENSP00000514867.1:n.1420_1429delinsCGTGTGAGCA
ENST00000700231.1:c.*83_*92delinsCGTGTGAGCA ENSP00000514868.1:n.*83_*92delinsCGTGTGAGCA
ENST00000339562.9:c.*83_*92delinsCGTGTGAGCA MANE Select ENSP00000344479.4:n.*83_*92delinsCGTGTGAGCA
ENST00000675870.1:c.*391_*400delinsCGTGTGAGCA ENSP00000502739.1:n.*391_*400delinsCGTGTGAGCA
ENST00000339562.8:c.*83_*92delinsCGTGTGAGCA ENSP00000344479.4:n.*83_*92delinsCGTGTGAGCA
ENST00000409572.5:c.*83_*92delinsCGTGTGAGCA ENSP00000386747.1:n.*83_*92delinsCGTGTGAGCA
ENST00000417764.5:c.*391_*400delinsCGTGTGAGCA ENSP00000415632.1:n.*391_*400delinsCGTGTGAGCA
ENST00000417972.5:c.*391_*400delinsCGTGTGAGCA ENSP00000394671.1:n.*391_*400delinsCGTGTGAGCA
ENST00000426264.5:c.*83_*92delinsCGTGTGAGCA ENSP00000389986.1:n.*83_*92delinsCGTGTGAGCA
NM_006186.3:c.*83_*92delinsCGTGTGAGCA NP_006177.1:n.*83_*92delinsCGTGTGAGCA
XM_005246621.2:c.*83_*92delinsCGTGTGAGCA XP_005246678.1:n.*83_*92delinsCGTGTGAGCA
XM_005246622.2:c.*83_*92delinsCGTGTGAGCA XP_005246679.1:n.*83_*92delinsCGTGTGAGCA
XM_005246623.1:c.*83_*92delinsCGTGTGAGCA XP_005246680.1:n.*83_*92delinsCGTGTGAGCA
XM_006712553.2:c.*83_*92delinsCGTGTGAGCA XP_006712616.1:n.*83_*92delinsCGTGTGAGCA
XM_011511246.1:c.*114_*123delinsCGTGTGAGCA XP_011509548.1:n.*114_*123delinsCGTGTGAGCA
NM_173173.2:c.*83_*92delinsCGTGTGAGCA NP_775265.1:n.*83_*92delinsCGTGTGAGCA
XM_005246621.4:c.*83_*92delinsCGTGTGAGCA XP_005246678.1:n.*83_*92delinsCGTGTGAGCA
XM_006712553.4:c.*83_*92delinsCGTGTGAGCA XP_006712616.1:n.*83_*92delinsCGTGTGAGCA
XM_011511246.2:c.*114_*123delinsCGTGTGAGCA XP_011509548.1:n.*114_*123delinsCGTGTGAGCA
XM_017004219.2:c.*83_*92delinsCGTGTGAGCA XP_016859708.1:n.*83_*92delinsCGTGTGAGCA
XM_017004220.2:c.*83_*92delinsCGTGTGAGCA XP_016859709.1:n.*83_*92delinsCGTGTGAGCA
XR_001738751.2:n.2127_2136delinsCGTGTGAGCA
XR_001738752.2:n.1949_1958delinsCGTGTGAGCA
XR_427087.4:n.2006_2015delinsCGTGTGAGCA
NM_006186.4:c.*83_*92delinsCGTGTGAGCA MANE Select NP_006177.1:n.*83_*92delinsCGTGTGAGCA
NM_173173.3:c.*83_*92delinsCGTGTGAGCA NP_775265.1:n.*83_*92delinsCGTGTGAGCA