Canonical Allele Identifier: CA348682960
Gene: NR4A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156329985T>G , CM000664.2:g.156329985T>G GRCh38
NC_000002.11:g.157186497T>G , CM000664.1:g.157186497T>G GRCh37
NC_000002.10:g.156894743T>G NCBI36
NG_011821.1:g.7791A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000421709.2:c.13A>C ENSP00000388120.2:p.Ser5Arg
ENST00000700228.1:c.73A>C ENSP00000514865.1:p.Ser25Arg
ENST00000700231.1:c.202A>C ENSP00000514868.1:p.Ser68Arg
ENST00000339562.9:c.202A>C MANE Select ENSP00000344479.4:p.Ser68Arg
ENST00000675870.1:c.13A>C ENSP00000502739.1:p.Ser5Arg
ENST00000339562.8:c.202A>C ENSP00000344479.4:p.Ser68Arg
ENST00000406048.2:c.137A>C
ENST00000409108.6:c.202A>C ENSP00000386993.2:p.Ser68Arg
ENST00000409572.5:c.202A>C ENSP00000386747.1:p.Ser68Arg
ENST00000417764.5:c.13A>C ENSP00000415632.1:p.Ser5Arg
ENST00000417972.5:c.13A>C ENSP00000394671.1:p.Ser5Arg
ENST00000421709.1:c.13A>C ENSP00000388120.1:p.Ser5Arg
ENST00000424077.1:c.202A>C ENSP00000406808.1:p.Ser68Arg
ENST00000426264.5:c.13A>C ENSP00000389986.1:p.Ser5Arg
ENST00000429376.5:c.13A>C ENSP00000410952.1:p.Ser5Arg
NM_006186.3:c.202A>C NP_006177.1:p.Ser68Arg
XM_005246621.2:c.235A>C XP_005246678.1:p.Ser79Arg
XM_005246622.2:c.13A>C XP_005246679.1:p.Ser5Arg
XM_005246623.1:c.13A>C XP_005246680.1:p.Ser5Arg
XM_006712553.2:c.235A>C XP_006712616.1:p.Ser79Arg
XM_011511246.1:c.235A>C XP_011509548.1:p.Ser79Arg
XR_427087.2:n.2408A>C
NM_173173.2:c.13A>C NP_775265.1:p.Ser5Arg
XM_005246621.4:c.235A>C XP_005246678.1:p.Ser79Arg
XM_006712553.4:c.235A>C XP_006712616.1:p.Ser79Arg
XM_011511246.2:c.235A>C XP_011509548.1:p.Ser79Arg
XM_017004219.2:c.202A>C XP_016859708.1:p.Ser68Arg
XM_017004220.2:c.202A>C XP_016859709.1:p.Ser68Arg
XR_001738751.2:n.570A>C
XR_001738752.2:n.392A>C
XR_427087.4:n.449A>C
NM_006186.4:c.202A>C MANE Select NP_006177.1:p.Ser68Arg
NM_173173.3:c.13A>C NP_775265.1:p.Ser5Arg