Canonical Allele Identifier: CA59154808
Gene: NR4A2 HGNC NCBI

Linked Data

dbSNP Id: rs557351028

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156326198T>C , CM000664.2:g.156326198T>C GRCh38
NC_000002.11:g.157182710T>C , CM000664.1:g.157182710T>C GRCh37
NC_000002.10:g.156890956T>C NCBI36
NG_011821.1:g.11578A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000700228.1:c.1288A>G ENSP00000514865.1:p.Ile430Val
ENST00000700229.1:c.456A>G
ENST00000700230.1:c.1032A>G ENSP00000514867.1:n.1032A>G
ENST00000700231.1:c.1417A>G ENSP00000514868.1:p.Ile473Val
ENST00000339562.9:c.1492A>G MANE Select ENSP00000344479.4:p.Ile498Val
ENST00000675870.1:c.*3A>G ENSP00000502739.1:n.*3A>G
ENST00000339562.8:c.1492A>G ENSP00000344479.4:p.Ile498Val
ENST00000409108.6:c.1388A>G ENSP00000386993.2:p.His463Arg
ENST00000409572.5:c.1492A>G ENSP00000386747.1:p.Ile498Val
ENST00000417764.5:c.*3A>G ENSP00000415632.1:n.*3A>G
ENST00000417972.5:c.*3A>G ENSP00000394671.1:n.*3A>G
ENST00000426264.5:c.1303A>G ENSP00000389986.1:p.Ile435Val
ENST00000429376.5:c.1199A>G ENSP00000410952.1:p.His400Arg
NM_006186.3:c.1492A>G NP_006177.1:p.Ile498Val
XM_005246621.2:c.1525A>G XP_005246678.1:p.Ile509Val
XM_005246622.2:c.1303A>G XP_005246679.1:p.Ile435Val
XM_005246623.1:c.1303A>G XP_005246680.1:p.Ile435Val
XM_006712553.2:c.1450A>G XP_006712616.1:p.Ile484Val
XM_011511246.1:c.1421A>G XP_011509548.1:p.His474Arg
XR_427087.2:n.3577A>G
NM_173173.2:c.1303A>G NP_775265.1:p.Ile435Val
XM_005246621.4:c.1525A>G XP_005246678.1:p.Ile509Val
XM_006712553.4:c.1450A>G XP_006712616.1:p.Ile484Val
XM_011511246.2:c.1421A>G XP_011509548.1:p.His474Arg
XM_017004219.2:c.1492A>G XP_016859708.1:p.Ile498Val
XM_017004220.2:c.1417A>G XP_016859709.1:p.Ile473Val
XR_001738751.2:n.1739A>G
XR_001738752.2:n.1561A>G
XR_427087.4:n.1618A>G
NM_006186.4:c.1492A>G MANE Select NP_006177.1:p.Ile498Val
NM_173173.3:c.1303A>G NP_775265.1:p.Ile435Val