Canonical Allele Identifier: CA1300460559

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329696T= , CM000664.2:g.156329696T=	GRCh38
NC_000002.11:g.157186208T= , CM000664.1:g.157186208T=	GRCh37
NC_000002.10:g.156894454T=	NCBI36
NG_011821.1:g.8080A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.302A=	ENSP00000388120.2:p.Glu101=
ENST00000700228.1:c.362A=	ENSP00000514865.1:p.Glu121=
ENST00000700231.1:c.491A=	ENSP00000514868.1:p.Glu164=
ENST00000339562.9:c.491A= MANE Select	ENSP00000344479.4:p.Glu164=
ENST00000675870.1:c.302A=	ENSP00000502739.1:p.Glu101=
ENST00000339562.8:c.491A=	ENSP00000344479.4:p.Glu164=
ENST00000406048.2:c.208+218A=
ENST00000409108.6:c.491A=	ENSP00000386993.2:p.Glu164=
ENST00000409572.5:c.491A=	ENSP00000386747.1:p.Glu164=
ENST00000417764.5:c.302A=	ENSP00000415632.1:p.Glu101=
ENST00000417972.5:c.302A=	ENSP00000394671.1:p.Glu101=
ENST00000421709.1:c.302A=	ENSP00000388120.1:p.Glu101=
ENST00000424077.1:c.491A=	ENSP00000406808.1:p.Glu164=
ENST00000426264.5:c.302A=	ENSP00000389986.1:p.Glu101=
ENST00000429376.5:c.302A=	ENSP00000410952.1:p.Glu101=
NM_006186.3:c.491A=	NP_006177.1:p.Glu164=
XM_005246621.2:c.524A=	XP_005246678.1:p.Glu175=
XM_005246622.2:c.302A=	XP_005246679.1:p.Glu101=
XM_005246623.1:c.302A=	XP_005246680.1:p.Glu101=
XM_006712553.2:c.524A=	XP_006712616.1:p.Glu175=
XM_011511246.1:c.524A=	XP_011509548.1:p.Glu175=
XR_427087.2:n.2697A=
NM_173173.2:c.302A=	NP_775265.1:p.Glu101=
XM_005246621.4:c.524A=	XP_005246678.1:p.Glu175=
XM_006712553.4:c.524A=	XP_006712616.1:p.Glu175=
XM_011511246.2:c.524A=	XP_011509548.1:p.Glu175=
XM_017004219.2:c.491A=	XP_016859708.1:p.Glu164=
XM_017004220.2:c.491A=	XP_016859709.1:p.Glu164=
XR_001738751.2:n.859A=
XR_001738752.2:n.681A=
XR_427087.4:n.738A=
NM_006186.4:c.491A= MANE Select	NP_006177.1:p.Glu164=
NM_173173.3:c.302A=	NP_775265.1:p.Glu101=