Canonical Allele Identifier: CA1300458903

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325858T= , CM000664.2:g.156325858T=	GRCh38
NC_000002.11:g.157182370T= , CM000664.1:g.157182370T=	GRCh37
NC_000002.10:g.156890616T=	NCBI36
NG_011821.1:g.11918A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1479A=	ENSP00000514865.1:p.Glu493=
ENST00000700229.1:c.647A=
ENST00000700230.1:c.1223A=	ENSP00000514867.1:n.1223A=
ENST00000700231.1:c.1608A=	ENSP00000514868.1:p.Glu536=
ENST00000339562.9:c.1683A= MANE Select	ENSP00000344479.4:p.Glu561=
ENST00000675870.1:c.*194A=	ENSP00000502739.1:n.*194A=
ENST00000339562.8:c.1683A=	ENSP00000344479.4:p.Glu561=
ENST00000409108.6:c.1579A=	ENSP00000386993.2:p.Thr527=
ENST00000409572.5:c.1683A=	ENSP00000386747.1:p.Glu561=
ENST00000417764.5:c.*194A=	ENSP00000415632.1:n.*194A=
ENST00000417972.5:c.*194A=	ENSP00000394671.1:n.*194A=
ENST00000426264.5:c.1494A=	ENSP00000389986.1:p.Glu498=
ENST00000429376.5:c.1390A=	ENSP00000410952.1:p.Thr464=
NM_006186.3:c.1683A=	NP_006177.1:p.Glu561=
XM_005246621.2:c.1716A=	XP_005246678.1:p.Glu572=
XM_005246622.2:c.1494A=	XP_005246679.1:p.Glu498=
XM_005246623.1:c.1494A=	XP_005246680.1:p.Glu498=
XM_006712553.2:c.1641A=	XP_006712616.1:p.Glu547=
XM_011511246.1:c.1612A=	XP_011509548.1:p.Thr538=
NM_173173.2:c.1494A=	NP_775265.1:p.Glu498=
XM_005246621.4:c.1716A=	XP_005246678.1:p.Glu572=
XM_006712553.4:c.1641A=	XP_006712616.1:p.Glu547=
XM_011511246.2:c.1612A=	XP_011509548.1:p.Thr538=
XM_017004219.2:c.1683A=	XP_016859708.1:p.Glu561=
XM_017004220.2:c.1608A=	XP_016859709.1:p.Glu536=
XR_001738751.2:n.1930A=
XR_001738752.2:n.1752A=
XR_427087.4:n.1809A=
NM_006186.4:c.1683A= MANE Select	NP_006177.1:p.Glu561=
NM_173173.3:c.1494A=	NP_775265.1:p.Glu498=