Canonical Allele Identifier: CA348682858
Gene: NR4A2 HGNC NCBI

Linked Data

dbSNP Id: rs1403697315

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156329942G>A , CM000664.2:g.156329942G>A GRCh38
NC_000002.11:g.157186454G>A , CM000664.1:g.157186454G>A GRCh37
NC_000002.10:g.156894700G>A NCBI36
NG_011821.1:g.7834C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000421709.2:c.56C>T ENSP00000388120.2:p.Pro19Leu
ENST00000700228.1:c.116C>T ENSP00000514865.1:p.Pro39Leu
ENST00000700231.1:c.245C>T ENSP00000514868.1:p.Pro82Leu
ENST00000339562.9:c.245C>T MANE Select ENSP00000344479.4:p.Pro82Leu
ENST00000675870.1:c.56C>T ENSP00000502739.1:p.Pro19Leu
ENST00000339562.8:c.245C>T ENSP00000344479.4:p.Pro82Leu
ENST00000406048.2:c.180C>T
ENST00000409108.6:c.245C>T ENSP00000386993.2:p.Pro82Leu
ENST00000409572.5:c.245C>T ENSP00000386747.1:p.Pro82Leu
ENST00000417764.5:c.56C>T ENSP00000415632.1:p.Pro19Leu
ENST00000417972.5:c.56C>T ENSP00000394671.1:p.Pro19Leu
ENST00000421709.1:c.56C>T ENSP00000388120.1:p.Pro19Leu
ENST00000424077.1:c.245C>T ENSP00000406808.1:p.Pro82Leu
ENST00000426264.5:c.56C>T ENSP00000389986.1:p.Pro19Leu
ENST00000429376.5:c.56C>T ENSP00000410952.1:p.Pro19Leu
NM_006186.3:c.245C>T NP_006177.1:p.Pro82Leu
XM_005246621.2:c.278C>T XP_005246678.1:p.Pro93Leu
XM_005246622.2:c.56C>T XP_005246679.1:p.Pro19Leu
XM_005246623.1:c.56C>T XP_005246680.1:p.Pro19Leu
XM_006712553.2:c.278C>T XP_006712616.1:p.Pro93Leu
XM_011511246.1:c.278C>T XP_011509548.1:p.Pro93Leu
XR_427087.2:n.2451C>T
NM_173173.2:c.56C>T NP_775265.1:p.Pro19Leu
XM_005246621.4:c.278C>T XP_005246678.1:p.Pro93Leu
XM_006712553.4:c.278C>T XP_006712616.1:p.Pro93Leu
XM_011511246.2:c.278C>T XP_011509548.1:p.Pro93Leu
XM_017004219.2:c.245C>T XP_016859708.1:p.Pro82Leu
XM_017004220.2:c.245C>T XP_016859709.1:p.Pro82Leu
XR_001738751.2:n.613C>T
XR_001738752.2:n.435C>T
XR_427087.4:n.492C>T
NM_006186.4:c.245C>T MANE Select NP_006177.1:p.Pro82Leu
NM_173173.3:c.56C>T NP_775265.1:p.Pro19Leu