Canonical Allele Identifier: CA348679961
Gene: NR4A2 HGNC NCBI

Linked Data

dbSNP Id: rs1371554953

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156326162C>T , CM000664.2:g.156326162C>T GRCh38
NC_000002.11:g.157182674C>T , CM000664.1:g.157182674C>T GRCh37
NC_000002.10:g.156890920C>T NCBI36
NG_011821.1:g.11614G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700228.1:c.1324G>A ENSP00000514865.1:p.Ala442Thr
ENST00000700229.1:c.492G>A
ENST00000700230.1:c.1068G>A ENSP00000514867.1:n.1068G>A
ENST00000700231.1:c.1453G>A ENSP00000514868.1:p.Ala485Thr
ENST00000339562.9:c.1528G>A MANE Select ENSP00000344479.4:p.Ala510Thr
ENST00000675870.1:c.*39G>A ENSP00000502739.1:n.*39G>A
ENST00000339562.8:c.1528G>A ENSP00000344479.4:p.Ala510Thr
ENST00000409108.6:c.1424G>A ENSP00000386993.2:p.Gly475Asp
ENST00000409572.5:c.1528G>A ENSP00000386747.1:p.Ala510Thr
ENST00000417764.5:c.*39G>A ENSP00000415632.1:n.*39G>A
ENST00000417972.5:c.*39G>A ENSP00000394671.1:n.*39G>A
ENST00000426264.5:c.1339G>A ENSP00000389986.1:p.Ala447Thr
ENST00000429376.5:c.1235G>A ENSP00000410952.1:p.Gly412Asp
NM_006186.3:c.1528G>A NP_006177.1:p.Ala510Thr
XM_005246621.2:c.1561G>A XP_005246678.1:p.Ala521Thr
XM_005246622.2:c.1339G>A XP_005246679.1:p.Ala447Thr
XM_005246623.1:c.1339G>A XP_005246680.1:p.Ala447Thr
XM_006712553.2:c.1486G>A XP_006712616.1:p.Ala496Thr
XM_011511246.1:c.1457G>A XP_011509548.1:p.Gly486Asp
XR_427087.2:n.3613G>A
NM_173173.2:c.1339G>A NP_775265.1:p.Ala447Thr
XM_005246621.4:c.1561G>A XP_005246678.1:p.Ala521Thr
XM_006712553.4:c.1486G>A XP_006712616.1:p.Ala496Thr
XM_011511246.2:c.1457G>A XP_011509548.1:p.Gly486Asp
XM_017004219.2:c.1528G>A XP_016859708.1:p.Ala510Thr
XM_017004220.2:c.1453G>A XP_016859709.1:p.Ala485Thr
XR_001738751.2:n.1775G>A
XR_001738752.2:n.1597G>A
XR_427087.4:n.1654G>A
NM_006186.4:c.1528G>A MANE Select NP_006177.1:p.Ala510Thr
NM_173173.3:c.1339G>A NP_775265.1:p.Ala447Thr