Canonical Allele Identifier: CA348679307
Gene: NR4A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156325781A>G , CM000664.2:g.156325781A>G GRCh38
NC_000002.11:g.157182293A>G , CM000664.1:g.157182293A>G GRCh37
NC_000002.10:g.156890539A>G NCBI36
NG_011821.1:g.11995T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000700228.1:c.1556T>C ENSP00000514865.1:p.Ile519Thr
ENST00000700229.1:c.724T>C
ENST00000700230.1:c.1300T>C ENSP00000514867.1:n.1300T>C
ENST00000700231.1:c.1685T>C ENSP00000514868.1:p.Ile562Thr
ENST00000339562.9:c.1760T>C MANE Select ENSP00000344479.4:p.Ile587Thr
ENST00000675870.1:c.*271T>C ENSP00000502739.1:n.*271T>C
ENST00000339562.8:c.1760T>C ENSP00000344479.4:p.Ile587Thr
ENST00000409108.6:c.1656T>C ENSP00000386993.2:p.Asn552=
ENST00000409572.5:c.1760T>C ENSP00000386747.1:p.Ile587Thr
ENST00000417764.5:c.*271T>C ENSP00000415632.1:n.*271T>C
ENST00000417972.5:c.*271T>C ENSP00000394671.1:n.*271T>C
ENST00000426264.5:c.1571T>C ENSP00000389986.1:p.Ile524Thr
ENST00000429376.5:c.1467T>C ENSP00000410952.1:p.Asn489=
NM_006186.3:c.1760T>C NP_006177.1:p.Ile587Thr
XM_005246621.2:c.1793T>C XP_005246678.1:p.Ile598Thr
XM_005246622.2:c.1571T>C XP_005246679.1:p.Ile524Thr
XM_005246623.1:c.1571T>C XP_005246680.1:p.Ile524Thr
XM_006712553.2:c.1718T>C XP_006712616.1:p.Ile573Thr
XM_011511246.1:c.1689T>C XP_011509548.1:p.Asn563=
NM_173173.2:c.1571T>C NP_775265.1:p.Ile524Thr
XM_005246621.4:c.1793T>C XP_005246678.1:p.Ile598Thr
XM_006712553.4:c.1718T>C XP_006712616.1:p.Ile573Thr
XM_011511246.2:c.1689T>C XP_011509548.1:p.Asn563=
XM_017004219.2:c.1760T>C XP_016859708.1:p.Ile587Thr
XM_017004220.2:c.1685T>C XP_016859709.1:p.Ile562Thr
XR_001738751.2:n.2007T>C
XR_001738752.2:n.1829T>C
XR_427087.4:n.1886T>C
NM_006186.4:c.1760T>C MANE Select NP_006177.1:p.Ile587Thr
NM_173173.3:c.1571T>C NP_775265.1:p.Ile524Thr