Canonical Allele Identifier: CA1300459025

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326201T= , CM000664.2:g.156326201T=	GRCh38
NC_000002.11:g.157182713T= , CM000664.1:g.157182713T=	GRCh37
NC_000002.10:g.156890959T=	NCBI36
NG_011821.1:g.11575A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1285A=	ENSP00000514865.1:p.Asn429=
ENST00000700229.1:c.453A=
ENST00000700230.1:c.1029A=	ENSP00000514867.1:n.1029A=
ENST00000700231.1:c.1414A=	ENSP00000514868.1:p.Asn472=
ENST00000339562.9:c.1489A= MANE Select	ENSP00000344479.4:p.Asn497=
ENST00000675870.1:c.1179A=	ENSP00000502739.1:p.Ter393=
ENST00000339562.8:c.1489A=	ENSP00000344479.4:p.Asn497=
ENST00000409108.6:c.1385A=	ENSP00000386993.2:p.Glu462=
ENST00000409572.5:c.1489A=	ENSP00000386747.1:p.Asn497=
ENST00000417764.5:c.1179A=	ENSP00000415632.1:p.Ter393=
ENST00000417972.5:c.1179A=	ENSP00000394671.1:p.Ter393=
ENST00000426264.5:c.1300A=	ENSP00000389986.1:p.Asn434=
ENST00000429376.5:c.1196A=	ENSP00000410952.1:p.Glu399=
NM_006186.3:c.1489A=	NP_006177.1:p.Asn497=
XM_005246621.2:c.1522A=	XP_005246678.1:p.Asn508=
XM_005246622.2:c.1300A=	XP_005246679.1:p.Asn434=
XM_005246623.1:c.1300A=	XP_005246680.1:p.Asn434=
XM_006712553.2:c.1447A=	XP_006712616.1:p.Asn483=
XM_011511246.1:c.1418A=	XP_011509548.1:p.Glu473=
XR_427087.2:n.3574A=
NM_173173.2:c.1300A=	NP_775265.1:p.Asn434=
XM_005246621.4:c.1522A=	XP_005246678.1:p.Asn508=
XM_006712553.4:c.1447A=	XP_006712616.1:p.Asn483=
XM_011511246.2:c.1418A=	XP_011509548.1:p.Glu473=
XM_017004219.2:c.1489A=	XP_016859708.1:p.Asn497=
XM_017004220.2:c.1414A=	XP_016859709.1:p.Asn472=
XR_001738751.2:n.1736A=
XR_001738752.2:n.1558A=
XR_427087.4:n.1615A=
NM_006186.4:c.1489A= MANE Select	NP_006177.1:p.Asn497=
NM_173173.3:c.1300A=	NP_775265.1:p.Asn434=