Canonical Allele Identifier: CA429727837
Gene: NR4A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156329862_156329863insC , CM000664.2:g.156329862_156329863insC GRCh38
NC_000002.11:g.157186374_157186375insC , CM000664.1:g.157186374_157186375insC GRCh37
NC_000002.10:g.156894620_156894621insC NCBI36
NG_011821.1:g.7913_7914insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000421709.2:c.135_136insG ENSP00000388120.2:p.Gln46AlafsTer3
ENST00000700228.1:c.195_196insG ENSP00000514865.1:p.Gln66AlafsTer3
ENST00000700231.1:c.324_325insG ENSP00000514868.1:p.Gln109AlafsTer3
ENST00000339562.9:c.324_325insG MANE Select ENSP00000344479.4:p.Gln109AlafsTer3
ENST00000675870.1:c.135_136insG ENSP00000502739.1:p.Gln46AlafsTer3
ENST00000339562.8:c.324_325insG ENSP00000344479.4:p.Gln109AlafsTer3
ENST00000406048.2:c.208+51_208+52insG
ENST00000409108.6:c.324_325insG ENSP00000386993.2:p.Gln109AlafsTer3
ENST00000409572.5:c.324_325insG ENSP00000386747.1:p.Gln109AlafsTer3
ENST00000417764.5:c.135_136insG ENSP00000415632.1:p.Gln46AlafsTer3
ENST00000417972.5:c.135_136insG ENSP00000394671.1:p.Gln46AlafsTer3
ENST00000421709.1:c.135_136insG ENSP00000388120.1:p.Gln46AlafsTer3
ENST00000424077.1:c.324_325insG ENSP00000406808.1:p.Gln109AlafsTer3
ENST00000426264.5:c.135_136insG ENSP00000389986.1:p.Gln46AlafsTer3
ENST00000429376.5:c.135_136insG ENSP00000410952.1:p.Gln46AlafsTer3
NM_006186.3:c.324_325insG NP_006177.1:p.Gln109AlafsTer3
XM_005246621.2:c.357_358insG XP_005246678.1:p.Gln120AlafsTer3
XM_005246622.2:c.135_136insG XP_005246679.1:p.Gln46AlafsTer3
XM_005246623.1:c.135_136insG XP_005246680.1:p.Gln46AlafsTer3
XM_006712553.2:c.357_358insG XP_006712616.1:p.Gln120AlafsTer3
XM_011511246.1:c.357_358insG XP_011509548.1:p.Gln120AlafsTer3
XR_427087.2:n.2530_2531insG
NM_173173.2:c.135_136insG NP_775265.1:p.Gln46AlafsTer3
XM_005246621.4:c.357_358insG XP_005246678.1:p.Gln120AlafsTer3
XM_006712553.4:c.357_358insG XP_006712616.1:p.Gln120AlafsTer3
XM_011511246.2:c.357_358insG XP_011509548.1:p.Gln120AlafsTer3
XM_017004219.2:c.324_325insG XP_016859708.1:p.Gln109AlafsTer3
XM_017004220.2:c.324_325insG XP_016859709.1:p.Gln109AlafsTer3
XR_001738751.2:n.692_693insG
XR_001738752.2:n.514_515insG
XR_427087.4:n.571_572insG
NM_006186.4:c.324_325insG MANE Select NP_006177.1:p.Gln109AlafsTer3
NM_173173.3:c.135_136insG NP_775265.1:p.Gln46AlafsTer3