Canonical Allele Identifier: CA1300458870

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325737G= , CM000664.2:g.156325737G=	GRCh38
NC_000002.11:g.157182249G= , CM000664.1:g.157182249G=	GRCh37
NC_000002.10:g.156890495G=	NCBI36
NG_011821.1:g.12039C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.*7C=	ENSP00000514865.1:n.*7C=
ENST00000700229.1:c.768C=
ENST00000700230.1:c.1344C=	ENSP00000514867.1:n.1344C=
ENST00000700231.1:c.*7C=	ENSP00000514868.1:n.*7C=
ENST00000339562.9:c.*7C= MANE Select	ENSP00000344479.4:n.*7C=
ENST00000675870.1:c.*315C=	ENSP00000502739.1:n.*315C=
ENST00000339562.8:c.*7C=	ENSP00000344479.4:n.*7C=
ENST00000409572.5:c.*7C=	ENSP00000386747.1:n.*7C=
ENST00000417764.5:c.*315C=	ENSP00000415632.1:n.*315C=
ENST00000417972.5:c.*315C=	ENSP00000394671.1:n.*315C=
ENST00000426264.5:c.*7C=	ENSP00000389986.1:n.*7C=
NM_006186.3:c.*7C=	NP_006177.1:n.*7C=
XM_005246621.2:c.*7C=	XP_005246678.1:n.*7C=
XM_005246622.2:c.*7C=	XP_005246679.1:n.*7C=
XM_005246623.1:c.*7C=	XP_005246680.1:n.*7C=
XM_006712553.2:c.*7C=	XP_006712616.1:n.*7C=
XM_011511246.1:c.*38C=	XP_011509548.1:n.*38C=
NM_173173.2:c.*7C=	NP_775265.1:n.*7C=
XM_005246621.4:c.*7C=	XP_005246678.1:n.*7C=
XM_006712553.4:c.*7C=	XP_006712616.1:n.*7C=
XM_011511246.2:c.*38C=	XP_011509548.1:n.*38C=
XM_017004219.2:c.*7C=	XP_016859708.1:n.*7C=
XM_017004220.2:c.*7C=	XP_016859709.1:n.*7C=
XR_001738751.2:n.2051C=
XR_001738752.2:n.1873C=
XR_427087.4:n.1930C=
NM_006186.4:c.*7C= MANE Select	NP_006177.1:n.*7C=
NM_173173.3:c.*7C=	NP_775265.1:n.*7C=