Canonical Allele Identifier: CA1300459015

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326185G= , CM000664.2:g.156326185G=	GRCh38
NC_000002.11:g.157182697G= , CM000664.1:g.157182697G=	GRCh37
NC_000002.10:g.156890943G=	NCBI36
NG_011821.1:g.11591C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1301C=	ENSP00000514865.1:p.Ala434=
ENST00000700229.1:c.469C=
ENST00000700230.1:c.1045C=	ENSP00000514867.1:n.1045C=
ENST00000700231.1:c.1430C=	ENSP00000514868.1:p.Ala477=
ENST00000339562.9:c.1505C= MANE Select	ENSP00000344479.4:p.Ala502=
ENST00000675870.1:c.*16C=	ENSP00000502739.1:n.*16C=
ENST00000339562.8:c.1505C=	ENSP00000344479.4:p.Ala502=
ENST00000409108.6:c.1401C=	ENSP00000386993.2:p.Cys467=
ENST00000409572.5:c.1505C=	ENSP00000386747.1:p.Ala502=
ENST00000417764.5:c.*16C=	ENSP00000415632.1:n.*16C=
ENST00000417972.5:c.*16C=	ENSP00000394671.1:n.*16C=
ENST00000426264.5:c.1316C=	ENSP00000389986.1:p.Ala439=
ENST00000429376.5:c.1212C=	ENSP00000410952.1:p.Cys404=
NM_006186.3:c.1505C=	NP_006177.1:p.Ala502=
XM_005246621.2:c.1538C=	XP_005246678.1:p.Ala513=
XM_005246622.2:c.1316C=	XP_005246679.1:p.Ala439=
XM_005246623.1:c.1316C=	XP_005246680.1:p.Ala439=
XM_006712553.2:c.1463C=	XP_006712616.1:p.Ala488=
XM_011511246.1:c.1434C=	XP_011509548.1:p.Cys478=
XR_427087.2:n.3590C=
NM_173173.2:c.1316C=	NP_775265.1:p.Ala439=
XM_005246621.4:c.1538C=	XP_005246678.1:p.Ala513=
XM_006712553.4:c.1463C=	XP_006712616.1:p.Ala488=
XM_011511246.2:c.1434C=	XP_011509548.1:p.Cys478=
XM_017004219.2:c.1505C=	XP_016859708.1:p.Ala502=
XM_017004220.2:c.1430C=	XP_016859709.1:p.Ala477=
XR_001738751.2:n.1752C=
XR_001738752.2:n.1574C=
XR_427087.4:n.1631C=
NM_006186.4:c.1505C= MANE Select	NP_006177.1:p.Ala502=
NM_173173.3:c.1316C=	NP_775265.1:p.Ala439=