Canonical Allele Identifier: CA348682565
Gene: NR4A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156329810G>A , CM000664.2:g.156329810G>A GRCh38
NC_000002.11:g.157186322G>A , CM000664.1:g.157186322G>A GRCh37
NC_000002.10:g.156894568G>A NCBI36
NG_011821.1:g.7966C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000421709.2:c.188C>T ENSP00000388120.2:p.Ser63Leu
ENST00000700228.1:c.248C>T ENSP00000514865.1:p.Ser83Leu
ENST00000700231.1:c.377C>T ENSP00000514868.1:p.Ser126Leu
ENST00000339562.9:c.377C>T MANE Select ENSP00000344479.4:p.Ser126Leu
ENST00000675870.1:c.188C>T ENSP00000502739.1:p.Ser63Leu
ENST00000339562.8:c.377C>T ENSP00000344479.4:p.Ser126Leu
ENST00000406048.2:c.208+104C>T
ENST00000409108.6:c.377C>T ENSP00000386993.2:p.Ser126Leu
ENST00000409572.5:c.377C>T ENSP00000386747.1:p.Ser126Leu
ENST00000417764.5:c.188C>T ENSP00000415632.1:p.Ser63Leu
ENST00000417972.5:c.188C>T ENSP00000394671.1:p.Ser63Leu
ENST00000421709.1:c.188C>T ENSP00000388120.1:p.Ser63Leu
ENST00000424077.1:c.377C>T ENSP00000406808.1:p.Ser126Leu
ENST00000426264.5:c.188C>T ENSP00000389986.1:p.Ser63Leu
ENST00000429376.5:c.188C>T ENSP00000410952.1:p.Ser63Leu
NM_006186.3:c.377C>T NP_006177.1:p.Ser126Leu
XM_005246621.2:c.410C>T XP_005246678.1:p.Ser137Leu
XM_005246622.2:c.188C>T XP_005246679.1:p.Ser63Leu
XM_005246623.1:c.188C>T XP_005246680.1:p.Ser63Leu
XM_006712553.2:c.410C>T XP_006712616.1:p.Ser137Leu
XM_011511246.1:c.410C>T XP_011509548.1:p.Ser137Leu
XR_427087.2:n.2583C>T
NM_173173.2:c.188C>T NP_775265.1:p.Ser63Leu
XM_005246621.4:c.410C>T XP_005246678.1:p.Ser137Leu
XM_006712553.4:c.410C>T XP_006712616.1:p.Ser137Leu
XM_011511246.2:c.410C>T XP_011509548.1:p.Ser137Leu
XM_017004219.2:c.377C>T XP_016859708.1:p.Ser126Leu
XM_017004220.2:c.377C>T XP_016859709.1:p.Ser126Leu
XR_001738751.2:n.745C>T
XR_001738752.2:n.567C>T
XR_427087.4:n.624C>T
NM_006186.4:c.377C>T MANE Select NP_006177.1:p.Ser126Leu
NM_173173.3:c.188C>T NP_775265.1:p.Ser63Leu