Canonical Allele Identifier: CA1300458936

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325954G= , CM000664.2:g.156325954G=	GRCh38
NC_000002.11:g.157182466G= , CM000664.1:g.157182466G=	GRCh37
NC_000002.10:g.156890712G=	NCBI36
NG_011821.1:g.11822C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1383C=	ENSP00000514865.1:p.Asn461=
ENST00000700229.1:c.551C=
ENST00000700230.1:c.1127C=	ENSP00000514867.1:n.1127C=
ENST00000700231.1:c.1512C=	ENSP00000514868.1:p.Asn504=
ENST00000339562.9:c.1587C= MANE Select	ENSP00000344479.4:p.Asn529=
ENST00000675870.1:c.*98C=	ENSP00000502739.1:n.*98C=
ENST00000339562.8:c.1587C=	ENSP00000344479.4:p.Asn529=
ENST00000409108.6:c.1483C=	ENSP00000386993.2:p.Gln495=
ENST00000409572.5:c.1587C=	ENSP00000386747.1:p.Asn529=
ENST00000417764.5:c.*98C=	ENSP00000415632.1:n.*98C=
ENST00000417972.5:c.*98C=	ENSP00000394671.1:n.*98C=
ENST00000426264.5:c.1398C=	ENSP00000389986.1:p.Asn466=
ENST00000429376.5:c.1294C=	ENSP00000410952.1:p.Gln432=
NM_006186.3:c.1587C=	NP_006177.1:p.Asn529=
XM_005246621.2:c.1620C=	XP_005246678.1:p.Asn540=
XM_005246622.2:c.1398C=	XP_005246679.1:p.Asn466=
XM_005246623.1:c.1398C=	XP_005246680.1:p.Asn466=
XM_006712553.2:c.1545C=	XP_006712616.1:p.Asn515=
XM_011511246.1:c.1516C=	XP_011509548.1:p.Gln506=
NM_173173.2:c.1398C=	NP_775265.1:p.Asn466=
XM_005246621.4:c.1620C=	XP_005246678.1:p.Asn540=
XM_006712553.4:c.1545C=	XP_006712616.1:p.Asn515=
XM_011511246.2:c.1516C=	XP_011509548.1:p.Gln506=
XM_017004219.2:c.1587C=	XP_016859708.1:p.Asn529=
XM_017004220.2:c.1512C=	XP_016859709.1:p.Asn504=
XR_001738751.2:n.1834C=
XR_001738752.2:n.1656C=
XR_427087.4:n.1713C=
NM_006186.4:c.1587C= MANE Select	NP_006177.1:p.Asn529=
NM_173173.3:c.1398C=	NP_775265.1:p.Asn466=