Canonical Allele Identifier: CA1300460517

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329591T= , CM000664.2:g.156329591T=	GRCh38
NC_000002.11:g.157186103T= , CM000664.1:g.157186103T=	GRCh37
NC_000002.10:g.156894349T=	NCBI36
NG_011821.1:g.8185A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.407A=	ENSP00000388120.2:p.His136=
ENST00000700228.1:c.467A=	ENSP00000514865.1:p.His156=
ENST00000700230.1:c.29A=	ENSP00000514867.1:p.His10=
ENST00000700231.1:c.596A=	ENSP00000514868.1:p.His199=
ENST00000339562.9:c.596A= MANE Select	ENSP00000344479.4:p.His199=
ENST00000675870.1:c.407A=	ENSP00000502739.1:p.His136=
ENST00000339562.8:c.596A=	ENSP00000344479.4:p.His199=
ENST00000406048.2:c.208+323A=
ENST00000409108.6:c.596A=	ENSP00000386993.2:p.His199=
ENST00000409572.5:c.596A=	ENSP00000386747.1:p.His199=
ENST00000417764.5:c.407A=	ENSP00000415632.1:p.His136=
ENST00000417972.5:c.407A=	ENSP00000394671.1:p.His136=
ENST00000424077.1:c.596A=	ENSP00000406808.1:p.His199=
ENST00000426264.5:c.407A=	ENSP00000389986.1:p.His136=
ENST00000429376.5:c.407A=	ENSP00000410952.1:p.His136=
NM_006186.3:c.596A=	NP_006177.1:p.His199=
XM_005246621.2:c.629A=	XP_005246678.1:p.His210=
XM_005246622.2:c.407A=	XP_005246679.1:p.His136=
XM_005246623.1:c.407A=	XP_005246680.1:p.His136=
XM_006712553.2:c.629A=	XP_006712616.1:p.His210=
XM_011511246.1:c.629A=	XP_011509548.1:p.His210=
XR_427087.2:n.2802A=
NM_173173.2:c.407A=	NP_775265.1:p.His136=
XM_005246621.4:c.629A=	XP_005246678.1:p.His210=
XM_006712553.4:c.629A=	XP_006712616.1:p.His210=
XM_011511246.2:c.629A=	XP_011509548.1:p.His210=
XM_017004219.2:c.596A=	XP_016859708.1:p.His199=
XM_017004220.2:c.596A=	XP_016859709.1:p.His199=
XR_001738751.2:n.964A=
XR_001738752.2:n.786A=
XR_427087.4:n.843A=
NM_006186.4:c.596A= MANE Select	NP_006177.1:p.His199=
NM_173173.3:c.407A=	NP_775265.1:p.His136=