Canonical Allele Identifier: CA1300458894

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325829T= , CM000664.2:g.156325829T=	GRCh38
NC_000002.11:g.157182341T= , CM000664.1:g.157182341T=	GRCh37
NC_000002.10:g.156890587T=	NCBI36
NG_011821.1:g.11947A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1508A=	ENSP00000514865.1:p.Gln503=
ENST00000700229.1:c.676A=
ENST00000700230.1:c.1252A=	ENSP00000514867.1:n.1252A=
ENST00000700231.1:c.1637A=	ENSP00000514868.1:p.Gln546=
ENST00000339562.9:c.1712A= MANE Select	ENSP00000344479.4:p.Gln571=
ENST00000675870.1:c.*223A=	ENSP00000502739.1:n.*223A=
ENST00000339562.8:c.1712A=	ENSP00000344479.4:p.Gln571=
ENST00000409108.6:c.1608A=	ENSP00000386993.2:p.Thr536=
ENST00000409572.5:c.1712A=	ENSP00000386747.1:p.Gln571=
ENST00000417764.5:c.*223A=	ENSP00000415632.1:n.*223A=
ENST00000417972.5:c.*223A=	ENSP00000394671.1:n.*223A=
ENST00000426264.5:c.1523A=	ENSP00000389986.1:p.Gln508=
ENST00000429376.5:c.1419A=	ENSP00000410952.1:p.Thr473=
NM_006186.3:c.1712A=	NP_006177.1:p.Gln571=
XM_005246621.2:c.1745A=	XP_005246678.1:p.Gln582=
XM_005246622.2:c.1523A=	XP_005246679.1:p.Gln508=
XM_005246623.1:c.1523A=	XP_005246680.1:p.Gln508=
XM_006712553.2:c.1670A=	XP_006712616.1:p.Gln557=
XM_011511246.1:c.1641A=	XP_011509548.1:p.Thr547=
NM_173173.2:c.1523A=	NP_775265.1:p.Gln508=
XM_005246621.4:c.1745A=	XP_005246678.1:p.Gln582=
XM_006712553.4:c.1670A=	XP_006712616.1:p.Gln557=
XM_011511246.2:c.1641A=	XP_011509548.1:p.Thr547=
XM_017004219.2:c.1712A=	XP_016859708.1:p.Gln571=
XM_017004220.2:c.1637A=	XP_016859709.1:p.Gln546=
XR_001738751.2:n.1959A=
XR_001738752.2:n.1781A=
XR_427087.4:n.1838A=
NM_006186.4:c.1712A= MANE Select	NP_006177.1:p.Gln571=
NM_173173.3:c.1523A=	NP_775265.1:p.Gln508=