Canonical Allele Identifier: CA1300460587
Gene: NR4A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156329761C= , CM000664.2:g.156329761C= GRCh38
NC_000002.11:g.157186273C= , CM000664.1:g.157186273C= GRCh37
NC_000002.10:g.156894519C= NCBI36
NG_011821.1:g.8015G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000421709.2:c.237G= ENSP00000388120.2:p.Met79=
ENST00000700228.1:c.297G= ENSP00000514865.1:p.Met99=
ENST00000700231.1:c.426G= ENSP00000514868.1:p.Met142=
ENST00000339562.9:c.426G= MANE Select ENSP00000344479.4:p.Met142=
ENST00000675870.1:c.237G= ENSP00000502739.1:p.Met79=
ENST00000339562.8:c.426G= ENSP00000344479.4:p.Met142=
ENST00000406048.2:c.208+153G=
ENST00000409108.6:c.426G= ENSP00000386993.2:p.Met142=
ENST00000409572.5:c.426G= ENSP00000386747.1:p.Met142=
ENST00000417764.5:c.237G= ENSP00000415632.1:p.Met79=
ENST00000417972.5:c.237G= ENSP00000394671.1:p.Met79=
ENST00000421709.1:c.237G= ENSP00000388120.1:p.Met79=
ENST00000424077.1:c.426G= ENSP00000406808.1:p.Met142=
ENST00000426264.5:c.237G= ENSP00000389986.1:p.Met79=
ENST00000429376.5:c.237G= ENSP00000410952.1:p.Met79=
NM_006186.3:c.426G= NP_006177.1:p.Met142=
XM_005246621.2:c.459G= XP_005246678.1:p.Met153=
XM_005246622.2:c.237G= XP_005246679.1:p.Met79=
XM_005246623.1:c.237G= XP_005246680.1:p.Met79=
XM_006712553.2:c.459G= XP_006712616.1:p.Met153=
XM_011511246.1:c.459G= XP_011509548.1:p.Met153=
XR_427087.2:n.2632G=
NM_173173.2:c.237G= NP_775265.1:p.Met79=
XM_005246621.4:c.459G= XP_005246678.1:p.Met153=
XM_006712553.4:c.459G= XP_006712616.1:p.Met153=
XM_011511246.2:c.459G= XP_011509548.1:p.Met153=
XM_017004219.2:c.426G= XP_016859708.1:p.Met142=
XM_017004220.2:c.426G= XP_016859709.1:p.Met142=
XR_001738751.2:n.794G=
XR_001738752.2:n.616G=
XR_427087.4:n.673G=
NM_006186.4:c.426G= MANE Select NP_006177.1:p.Met142=
NM_173173.3:c.237G= NP_775265.1:p.Met79=