Canonical Allele Identifier: CA348682546
Gene: NR4A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156329801G>A , CM000664.2:g.156329801G>A GRCh38
NC_000002.11:g.157186313G>A , CM000664.1:g.157186313G>A GRCh37
NC_000002.10:g.156894559G>A NCBI36
NG_011821.1:g.7975C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000421709.2:c.197C>T ENSP00000388120.2:p.Thr66Met
ENST00000700228.1:c.257C>T ENSP00000514865.1:p.Thr86Met
ENST00000700231.1:c.386C>T ENSP00000514868.1:p.Thr129Met
ENST00000339562.9:c.386C>T MANE Select ENSP00000344479.4:p.Thr129Met
ENST00000675870.1:c.197C>T ENSP00000502739.1:p.Thr66Met
ENST00000339562.8:c.386C>T ENSP00000344479.4:p.Thr129Met
ENST00000406048.2:c.208+113C>T
ENST00000409108.6:c.386C>T ENSP00000386993.2:p.Thr129Met
ENST00000409572.5:c.386C>T ENSP00000386747.1:p.Thr129Met
ENST00000417764.5:c.197C>T ENSP00000415632.1:p.Thr66Met
ENST00000417972.5:c.197C>T ENSP00000394671.1:p.Thr66Met
ENST00000421709.1:c.197C>T ENSP00000388120.1:p.Thr66Met
ENST00000424077.1:c.386C>T ENSP00000406808.1:p.Thr129Met
ENST00000426264.5:c.197C>T ENSP00000389986.1:p.Thr66Met
ENST00000429376.5:c.197C>T ENSP00000410952.1:p.Thr66Met
NM_006186.3:c.386C>T NP_006177.1:p.Thr129Met
XM_005246621.2:c.419C>T XP_005246678.1:p.Thr140Met
XM_005246622.2:c.197C>T XP_005246679.1:p.Thr66Met
XM_005246623.1:c.197C>T XP_005246680.1:p.Thr66Met
XM_006712553.2:c.419C>T XP_006712616.1:p.Thr140Met
XM_011511246.1:c.419C>T XP_011509548.1:p.Thr140Met
XR_427087.2:n.2592C>T
NM_173173.2:c.197C>T NP_775265.1:p.Thr66Met
XM_005246621.4:c.419C>T XP_005246678.1:p.Thr140Met
XM_006712553.4:c.419C>T XP_006712616.1:p.Thr140Met
XM_011511246.2:c.419C>T XP_011509548.1:p.Thr140Met
XM_017004219.2:c.386C>T XP_016859708.1:p.Thr129Met
XM_017004220.2:c.386C>T XP_016859709.1:p.Thr129Met
XR_001738751.2:n.754C>T
XR_001738752.2:n.576C>T
XR_427087.4:n.633C>T
NM_006186.4:c.386C>T MANE Select NP_006177.1:p.Thr129Met
NM_173173.3:c.197C>T NP_775265.1:p.Thr66Met