Canonical Allele Identifier: CA1300460442

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329454C= , CM000664.2:g.156329454C=	GRCh38
NC_000002.11:g.157185966C= , CM000664.1:g.157185966C=	GRCh37
NC_000002.10:g.156894212C=	NCBI36
NG_011821.1:g.8322G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.604G=	ENSP00000514865.1:p.Asp202=
ENST00000700230.1:c.166G=	ENSP00000514867.1:p.Asp56=
ENST00000700231.1:c.733G=	ENSP00000514868.1:p.Asp245=
ENST00000339562.9:c.733G= MANE Select	ENSP00000344479.4:p.Asp245=
ENST00000675870.1:c.544G=	ENSP00000502739.1:p.Asp182=
ENST00000339562.8:c.733G=	ENSP00000344479.4:p.Asp245=
ENST00000406048.2:c.208+460G=
ENST00000409108.6:c.733G=	ENSP00000386993.2:p.Asp245=
ENST00000409572.5:c.733G=	ENSP00000386747.1:p.Asp245=
ENST00000417764.5:c.544G=	ENSP00000415632.1:p.Asp182=
ENST00000417972.5:c.544G=	ENSP00000394671.1:p.Asp182=
ENST00000424077.1:c.733G=	ENSP00000406808.1:p.Asp245=
ENST00000426264.5:c.544G=	ENSP00000389986.1:p.Asp182=
ENST00000429376.5:c.544G=	ENSP00000410952.1:p.Asp182=
NM_006186.3:c.733G=	NP_006177.1:p.Asp245=
XM_005246621.2:c.766G=	XP_005246678.1:p.Asp256=
XM_005246622.2:c.544G=	XP_005246679.1:p.Asp182=
XM_005246623.1:c.544G=	XP_005246680.1:p.Asp182=
XM_006712553.2:c.766G=	XP_006712616.1:p.Asp256=
XM_011511246.1:c.766G=	XP_011509548.1:p.Asp256=
XR_427087.2:n.2939G=
NM_173173.2:c.544G=	NP_775265.1:p.Asp182=
XM_005246621.4:c.766G=	XP_005246678.1:p.Asp256=
XM_006712553.4:c.766G=	XP_006712616.1:p.Asp256=
XM_011511246.2:c.766G=	XP_011509548.1:p.Asp256=
XM_017004219.2:c.733G=	XP_016859708.1:p.Asp245=
XM_017004220.2:c.733G=	XP_016859709.1:p.Asp245=
XR_001738751.2:n.1101G=
XR_001738752.2:n.923G=
XR_427087.4:n.980G=
NM_006186.4:c.733G= MANE Select	NP_006177.1:p.Asp245=
NM_173173.3:c.544G=	NP_775265.1:p.Asp182=