Canonical Allele Identifier: CA1300458822

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325642G= , CM000664.2:g.156325642G=	GRCh38
NC_000002.11:g.157182154G= , CM000664.1:g.157182154G=	GRCh37
NC_000002.10:g.156890400G=	NCBI36
NG_011821.1:g.12134C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.*102C=	ENSP00000514865.1:n.*102C=
ENST00000700229.1:c.863C=
ENST00000700230.1:c.1439C=	ENSP00000514867.1:n.1439C=
ENST00000700231.1:c.*102C=	ENSP00000514868.1:n.*102C=
ENST00000339562.9:c.*102C= MANE Select	ENSP00000344479.4:n.*102C=
ENST00000675870.1:c.*410C=	ENSP00000502739.1:n.*410C=
ENST00000339562.8:c.*102C=	ENSP00000344479.4:n.*102C=
ENST00000409572.5:c.*102C=	ENSP00000386747.1:n.*102C=
ENST00000417764.5:c.*410C=	ENSP00000415632.1:n.*410C=
ENST00000417972.5:c.*410C=	ENSP00000394671.1:n.*410C=
ENST00000426264.5:c.*102C=	ENSP00000389986.1:n.*102C=
NM_006186.3:c.*102C=	NP_006177.1:n.*102C=
XM_005246621.2:c.*102C=	XP_005246678.1:n.*102C=
XM_005246622.2:c.*102C=	XP_005246679.1:n.*102C=
XM_005246623.1:c.*102C=	XP_005246680.1:n.*102C=
XM_006712553.2:c.*102C=	XP_006712616.1:n.*102C=
XM_011511246.1:c.*133C=	XP_011509548.1:n.*133C=
NM_173173.2:c.*102C=	NP_775265.1:n.*102C=
XM_005246621.4:c.*102C=	XP_005246678.1:n.*102C=
XM_006712553.4:c.*102C=	XP_006712616.1:n.*102C=
XM_011511246.2:c.*133C=	XP_011509548.1:n.*133C=
XM_017004219.2:c.*102C=	XP_016859708.1:n.*102C=
XM_017004220.2:c.*102C=	XP_016859709.1:n.*102C=
XR_001738751.2:n.2146C=
XR_001738752.2:n.1968C=
XR_427087.4:n.2025C=
NM_006186.4:c.*102C= MANE Select	NP_006177.1:n.*102C=
NM_173173.3:c.*102C=	NP_775265.1:n.*102C=