Canonical Allele Identifier: CA348679939
Gene: NR4A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156326154G>A , CM000664.2:g.156326154G>A GRCh38
NC_000002.11:g.157182666G>A , CM000664.1:g.157182666G>A GRCh37
NC_000002.10:g.156890912G>A NCBI36
NG_011821.1:g.11622C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700228.1:c.1332C>T ENSP00000514865.1:p.Val444=
ENST00000700229.1:c.500C>T
ENST00000700230.1:c.1076C>T ENSP00000514867.1:n.1076C>T
ENST00000700231.1:c.1461C>T ENSP00000514868.1:p.Val487=
ENST00000339562.9:c.1536C>T MANE Select ENSP00000344479.4:p.Val512=
ENST00000675870.1:c.*47C>T ENSP00000502739.1:n.*47C>T
ENST00000339562.8:c.1536C>T ENSP00000344479.4:p.Val512=
ENST00000409108.6:c.1432C>T ENSP00000386993.2:p.His478Tyr
ENST00000409572.5:c.1536C>T ENSP00000386747.1:p.Val512=
ENST00000417764.5:c.*47C>T ENSP00000415632.1:n.*47C>T
ENST00000417972.5:c.*47C>T ENSP00000394671.1:n.*47C>T
ENST00000426264.5:c.1347C>T ENSP00000389986.1:p.Val449=
ENST00000429376.5:c.1243C>T ENSP00000410952.1:p.His415Tyr
NM_006186.3:c.1536C>T NP_006177.1:p.Val512=
XM_005246621.2:c.1569C>T XP_005246678.1:p.Val523=
XM_005246622.2:c.1347C>T XP_005246679.1:p.Val449=
XM_005246623.1:c.1347C>T XP_005246680.1:p.Val449=
XM_006712553.2:c.1494C>T XP_006712616.1:p.Val498=
XM_011511246.1:c.1465C>T XP_011509548.1:p.His489Tyr
XR_427087.2:n.3621C>T
NM_173173.2:c.1347C>T NP_775265.1:p.Val449=
XM_005246621.4:c.1569C>T XP_005246678.1:p.Val523=
XM_006712553.4:c.1494C>T XP_006712616.1:p.Val498=
XM_011511246.2:c.1465C>T XP_011509548.1:p.His489Tyr
XM_017004219.2:c.1536C>T XP_016859708.1:p.Val512=
XM_017004220.2:c.1461C>T XP_016859709.1:p.Val487=
XR_001738751.2:n.1783C>T
XR_001738752.2:n.1605C>T
XR_427087.4:n.1662C>T
NM_006186.4:c.1536C>T MANE Select NP_006177.1:p.Val512=
NM_173173.3:c.1347C>T NP_775265.1:p.Val449=