Canonical Allele Identifier: CA1300459022

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326196G= , CM000664.2:g.156326196G=	GRCh38
NC_000002.11:g.157182708G= , CM000664.1:g.157182708G=	GRCh37
NC_000002.10:g.156890954G=	NCBI36
NG_011821.1:g.11580C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1290C=	ENSP00000514865.1:p.Ile430=
ENST00000700229.1:c.458C=
ENST00000700230.1:c.1034C=	ENSP00000514867.1:n.1034C=
ENST00000700231.1:c.1419C=	ENSP00000514868.1:p.Ile473=
ENST00000339562.9:c.1494C= MANE Select	ENSP00000344479.4:p.Ile498=
ENST00000675870.1:c.*5C=	ENSP00000502739.1:n.*5C=
ENST00000339562.8:c.1494C=	ENSP00000344479.4:p.Ile498=
ENST00000409108.6:c.1390C=	ENSP00000386993.2:p.Arg464=
ENST00000409572.5:c.1494C=	ENSP00000386747.1:p.Ile498=
ENST00000417764.5:c.*5C=	ENSP00000415632.1:n.*5C=
ENST00000417972.5:c.*5C=	ENSP00000394671.1:n.*5C=
ENST00000426264.5:c.1305C=	ENSP00000389986.1:p.Ile435=
ENST00000429376.5:c.1201C=	ENSP00000410952.1:p.Arg401=
NM_006186.3:c.1494C=	NP_006177.1:p.Ile498=
XM_005246621.2:c.1527C=	XP_005246678.1:p.Ile509=
XM_005246622.2:c.1305C=	XP_005246679.1:p.Ile435=
XM_005246623.1:c.1305C=	XP_005246680.1:p.Ile435=
XM_006712553.2:c.1452C=	XP_006712616.1:p.Ile484=
XM_011511246.1:c.1423C=	XP_011509548.1:p.Arg475=
XR_427087.2:n.3579C=
NM_173173.2:c.1305C=	NP_775265.1:p.Ile435=
XM_005246621.4:c.1527C=	XP_005246678.1:p.Ile509=
XM_006712553.4:c.1452C=	XP_006712616.1:p.Ile484=
XM_011511246.2:c.1423C=	XP_011509548.1:p.Arg475=
XM_017004219.2:c.1494C=	XP_016859708.1:p.Ile498=
XM_017004220.2:c.1419C=	XP_016859709.1:p.Ile473=
XR_001738751.2:n.1741C=
XR_001738752.2:n.1563C=
XR_427087.4:n.1620C=
NM_006186.4:c.1494C= MANE Select	NP_006177.1:p.Ile498=
NM_173173.3:c.1305C=	NP_775265.1:p.Ile435=