Canonical Allele Identifier: CA1300460655
Gene: NR4A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156329906T= , CM000664.2:g.156329906T= GRCh38
NC_000002.11:g.157186418T= , CM000664.1:g.157186418T= GRCh37
NC_000002.10:g.156894664T= NCBI36
NG_011821.1:g.7870A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000421709.2:c.92A= ENSP00000388120.2:p.Asp31=
ENST00000700228.1:c.152A= ENSP00000514865.1:p.Asp51=
ENST00000700231.1:c.281A= ENSP00000514868.1:p.Asp94=
ENST00000339562.9:c.281A= MANE Select ENSP00000344479.4:p.Asp94=
ENST00000675870.1:c.92A= ENSP00000502739.1:p.Asp31=
ENST00000339562.8:c.281A= ENSP00000344479.4:p.Asp94=
ENST00000406048.2:c.208+8A=
ENST00000409108.6:c.281A= ENSP00000386993.2:p.Asp94=
ENST00000409572.5:c.281A= ENSP00000386747.1:p.Asp94=
ENST00000417764.5:c.92A= ENSP00000415632.1:p.Asp31=
ENST00000417972.5:c.92A= ENSP00000394671.1:p.Asp31=
ENST00000421709.1:c.92A= ENSP00000388120.1:p.Asp31=
ENST00000424077.1:c.281A= ENSP00000406808.1:p.Asp94=
ENST00000426264.5:c.92A= ENSP00000389986.1:p.Asp31=
ENST00000429376.5:c.92A= ENSP00000410952.1:p.Asp31=
NM_006186.3:c.281A= NP_006177.1:p.Asp94=
XM_005246621.2:c.314A= XP_005246678.1:p.Asp105=
XM_005246622.2:c.92A= XP_005246679.1:p.Asp31=
XM_005246623.1:c.92A= XP_005246680.1:p.Asp31=
XM_006712553.2:c.314A= XP_006712616.1:p.Asp105=
XM_011511246.1:c.314A= XP_011509548.1:p.Asp105=
XR_427087.2:n.2487A=
NM_173173.2:c.92A= NP_775265.1:p.Asp31=
XM_005246621.4:c.314A= XP_005246678.1:p.Asp105=
XM_006712553.4:c.314A= XP_006712616.1:p.Asp105=
XM_011511246.2:c.314A= XP_011509548.1:p.Asp105=
XM_017004219.2:c.281A= XP_016859708.1:p.Asp94=
XM_017004220.2:c.281A= XP_016859709.1:p.Asp94=
XR_001738751.2:n.649A=
XR_001738752.2:n.471A=
XR_427087.4:n.528A=
NM_006186.4:c.281A= MANE Select NP_006177.1:p.Asp94=
NM_173173.3:c.92A= NP_775265.1:p.Asp31=