Canonical Allele Identifier: CA1300458904

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325863G= , CM000664.2:g.156325863G=	GRCh38
NC_000002.11:g.157182375G= , CM000664.1:g.157182375G=	GRCh37
NC_000002.10:g.156890621G=	NCBI36
NG_011821.1:g.11913C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1474C=	ENSP00000514865.1:p.Pro492=
ENST00000700229.1:c.642C=
ENST00000700230.1:c.1218C=	ENSP00000514867.1:n.1218C=
ENST00000700231.1:c.1603C=	ENSP00000514868.1:p.Pro535=
ENST00000339562.9:c.1678C= MANE Select	ENSP00000344479.4:p.Pro560=
ENST00000675870.1:c.*189C=	ENSP00000502739.1:n.*189C=
ENST00000339562.8:c.1678C=	ENSP00000344479.4:p.Pro560=
ENST00000409108.6:c.1574C=	ENSP00000386993.2:p.Pro525=
ENST00000409572.5:c.1678C=	ENSP00000386747.1:p.Pro560=
ENST00000417764.5:c.*189C=	ENSP00000415632.1:n.*189C=
ENST00000417972.5:c.*189C=	ENSP00000394671.1:n.*189C=
ENST00000426264.5:c.1489C=	ENSP00000389986.1:p.Pro497=
ENST00000429376.5:c.1385C=	ENSP00000410952.1:p.Pro462=
NM_006186.3:c.1678C=	NP_006177.1:p.Pro560=
XM_005246621.2:c.1711C=	XP_005246678.1:p.Pro571=
XM_005246622.2:c.1489C=	XP_005246679.1:p.Pro497=
XM_005246623.1:c.1489C=	XP_005246680.1:p.Pro497=
XM_006712553.2:c.1636C=	XP_006712616.1:p.Pro546=
XM_011511246.1:c.1607C=	XP_011509548.1:p.Pro536=
NM_173173.2:c.1489C=	NP_775265.1:p.Pro497=
XM_005246621.4:c.1711C=	XP_005246678.1:p.Pro571=
XM_006712553.4:c.1636C=	XP_006712616.1:p.Pro546=
XM_011511246.2:c.1607C=	XP_011509548.1:p.Pro536=
XM_017004219.2:c.1678C=	XP_016859708.1:p.Pro560=
XM_017004220.2:c.1603C=	XP_016859709.1:p.Pro535=
XR_001738751.2:n.1925C=
XR_001738752.2:n.1747C=
XR_427087.4:n.1804C=
NM_006186.4:c.1678C= MANE Select	NP_006177.1:p.Pro560=
NM_173173.3:c.1489C=	NP_775265.1:p.Pro497=