Canonical Allele Identifier: CA1300458950

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326000T= , CM000664.2:g.156326000T=	GRCh38
NC_000002.11:g.157182512T= , CM000664.1:g.157182512T=	GRCh37
NC_000002.10:g.156890758T=	NCBI36
NG_011821.1:g.11776A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1337A=	ENSP00000514865.1:p.Glu446=
ENST00000700229.1:c.505A=
ENST00000700230.1:c.1081A=	ENSP00000514867.1:n.1081A=
ENST00000700231.1:c.1466A=	ENSP00000514868.1:p.Glu489=
ENST00000339562.9:c.1541A= MANE Select	ENSP00000344479.4:p.Glu514=
ENST00000675870.1:c.*52A=	ENSP00000502739.1:n.*52A=
ENST00000339562.8:c.1541A=	ENSP00000344479.4:p.Glu514=
ENST00000409108.6:c.1437A=	ENSP00000386993.2:p.Arg479=
ENST00000409572.5:c.1541A=	ENSP00000386747.1:p.Glu514=
ENST00000417764.5:c.*52A=	ENSP00000415632.1:n.*52A=
ENST00000417972.5:c.*52A=	ENSP00000394671.1:n.*52A=
ENST00000426264.5:c.1352A=	ENSP00000389986.1:p.Glu451=
ENST00000429376.5:c.1248A=	ENSP00000410952.1:p.Arg416=
NM_006186.3:c.1541A=	NP_006177.1:p.Glu514=
XM_005246621.2:c.1574A=	XP_005246678.1:p.Glu525=
XM_005246622.2:c.1352A=	XP_005246679.1:p.Glu451=
XM_005246623.1:c.1352A=	XP_005246680.1:p.Glu451=
XM_006712553.2:c.1499A=	XP_006712616.1:p.Glu500=
XM_011511246.1:c.1470A=	XP_011509548.1:p.Arg490=
XR_427087.2:n.3626A=
NM_173173.2:c.1352A=	NP_775265.1:p.Glu451=
XM_005246621.4:c.1574A=	XP_005246678.1:p.Glu525=
XM_006712553.4:c.1499A=	XP_006712616.1:p.Glu500=
XM_011511246.2:c.1470A=	XP_011509548.1:p.Arg490=
XM_017004219.2:c.1541A=	XP_016859708.1:p.Glu514=
XM_017004220.2:c.1466A=	XP_016859709.1:p.Glu489=
XR_001738751.2:n.1788A=
XR_001738752.2:n.1610A=
XR_427087.4:n.1667A=
NM_006186.4:c.1541A= MANE Select	NP_006177.1:p.Glu514=
NM_173173.3:c.1352A=	NP_775265.1:p.Glu451=