Canonical Allele Identifier: CA2577126847
Gene: NR4A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156330116dup , CM000664.2:g.156330116dup GRCh38
NC_000002.11:g.157186628dup , CM000664.1:g.157186628dup GRCh37
NC_000002.10:g.156894874dup NCBI36
NG_011821.1:g.7660dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000421709.2:c.-13-106dup ENSP00000388120.2:n.-13-106dup
ENST00000700228.1:c.-59dup ENSP00000514865.1:n.-59dup
ENST00000700231.1:c.71dup ENSP00000514868.1:p.Tyr24Ter
ENST00000339562.9:c.71dup MANE Select ENSP00000344479.4:p.Tyr24Ter
ENST00000675870.1:c.-13-106dup ENSP00000502739.1:n.-13-106dup
ENST00000339562.8:c.71dup ENSP00000344479.4:p.Tyr24Ter
ENST00000406048.2:c.6dup
ENST00000409108.6:c.71dup ENSP00000386993.2:p.Tyr24Ter
ENST00000409572.5:c.71dup ENSP00000386747.1:p.Tyr24Ter
ENST00000417764.5:c.-13-106dup ENSP00000415632.1:n.-13-106dup
ENST00000417972.5:c.-13-106dup ENSP00000394671.1:n.-13-106dup
ENST00000421709.1:c.-13-106dup ENSP00000388120.1:n.-13-106dup
ENST00000424077.1:c.71dup ENSP00000406808.1:p.Tyr24Ter
ENST00000426264.5:c.-13-106dup ENSP00000389986.1:n.-13-106dup
ENST00000429376.5:c.-13-106dup ENSP00000410952.1:n.-13-106dup
NM_006186.3:c.71dup NP_006177.1:p.Tyr24Ter
XM_005246621.2:c.104dup XP_005246678.1:p.Tyr35Ter
XM_005246622.2:c.-13-106dup XP_005246679.1:n.-13-106dup
XM_005246623.1:c.-13-106dup XP_005246680.1:n.-13-106dup
XM_006712553.2:c.104dup XP_006712616.1:p.Tyr35Ter
XM_011511246.1:c.104dup XP_011509548.1:p.Tyr35Ter
XR_427087.2:n.2277dup
NM_173173.2:c.-13-106dup NP_775265.1:n.-13-106dup
XM_005246621.4:c.104dup XP_005246678.1:p.Tyr35Ter
XM_006712553.4:c.104dup XP_006712616.1:p.Tyr35Ter
XM_011511246.2:c.104dup XP_011509548.1:p.Tyr35Ter
XM_017004219.2:c.71dup XP_016859708.1:p.Tyr24Ter
XM_017004220.2:c.71dup XP_016859709.1:p.Tyr24Ter
XR_001738751.2:n.439dup
XR_001738752.2:n.367-106dup
XR_427087.4:n.318dup
NM_006186.4:c.71dup MANE Select NP_006177.1:p.Tyr24Ter
NM_173173.3:c.-13-106dup NP_775265.1:n.-13-106dup