Canonical Allele Identifier: CA348682033
Gene: NR4A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156329565C>A , CM000664.2:g.156329565C>A GRCh38
NC_000002.11:g.157186077C>A , CM000664.1:g.157186077C>A GRCh37
NC_000002.10:g.156894323C>A NCBI36
NG_011821.1:g.8211G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000421709.2:c.433G>T ENSP00000388120.2:p.Gly145Cys
ENST00000700228.1:c.493G>T ENSP00000514865.1:p.Gly165Cys
ENST00000700230.1:c.55G>T ENSP00000514867.1:p.Gly19Cys
ENST00000700231.1:c.622G>T ENSP00000514868.1:p.Gly208Cys
ENST00000339562.9:c.622G>T MANE Select ENSP00000344479.4:p.Gly208Cys
ENST00000675870.1:c.433G>T ENSP00000502739.1:p.Gly145Cys
ENST00000339562.8:c.622G>T ENSP00000344479.4:p.Gly208Cys
ENST00000406048.2:c.208+349G>T
ENST00000409108.6:c.622G>T ENSP00000386993.2:p.Gly208Cys
ENST00000409572.5:c.622G>T ENSP00000386747.1:p.Gly208Cys
ENST00000417764.5:c.433G>T ENSP00000415632.1:p.Gly145Cys
ENST00000417972.5:c.433G>T ENSP00000394671.1:p.Gly145Cys
ENST00000424077.1:c.622G>T ENSP00000406808.1:p.Gly208Cys
ENST00000426264.5:c.433G>T ENSP00000389986.1:p.Gly145Cys
ENST00000429376.5:c.433G>T ENSP00000410952.1:p.Gly145Cys
NM_006186.3:c.622G>T NP_006177.1:p.Gly208Cys
XM_005246621.2:c.655G>T XP_005246678.1:p.Gly219Cys
XM_005246622.2:c.433G>T XP_005246679.1:p.Gly145Cys
XM_005246623.1:c.433G>T XP_005246680.1:p.Gly145Cys
XM_006712553.2:c.655G>T XP_006712616.1:p.Gly219Cys
XM_011511246.1:c.655G>T XP_011509548.1:p.Gly219Cys
XR_427087.2:n.2828G>T
NM_173173.2:c.433G>T NP_775265.1:p.Gly145Cys
XM_005246621.4:c.655G>T XP_005246678.1:p.Gly219Cys
XM_006712553.4:c.655G>T XP_006712616.1:p.Gly219Cys
XM_011511246.2:c.655G>T XP_011509548.1:p.Gly219Cys
XM_017004219.2:c.622G>T XP_016859708.1:p.Gly208Cys
XM_017004220.2:c.622G>T XP_016859709.1:p.Gly208Cys
XR_001738751.2:n.990G>T
XR_001738752.2:n.812G>T
XR_427087.4:n.869G>T
NM_006186.4:c.622G>T MANE Select NP_006177.1:p.Gly208Cys
NM_173173.3:c.433G>T NP_775265.1:p.Gly145Cys