Canonical Allele Identifier: CA1300459019

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326193G= , CM000664.2:g.156326193G=	GRCh38
NC_000002.11:g.157182705G= , CM000664.1:g.157182705G=	GRCh37
NC_000002.10:g.156890951G=	NCBI36
NG_011821.1:g.11583C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1293C=	ENSP00000514865.1:p.Asp431=
ENST00000700229.1:c.461C=
ENST00000700230.1:c.1037C=	ENSP00000514867.1:n.1037C=
ENST00000700231.1:c.1422C=	ENSP00000514868.1:p.Asp474=
ENST00000339562.9:c.1497C= MANE Select	ENSP00000344479.4:p.Asp499=
ENST00000675870.1:c.*8C=	ENSP00000502739.1:n.*8C=
ENST00000339562.8:c.1497C=	ENSP00000344479.4:p.Asp499=
ENST00000409108.6:c.1393C=	ENSP00000386993.2:p.His465=
ENST00000409572.5:c.1497C=	ENSP00000386747.1:p.Asp499=
ENST00000417764.5:c.*8C=	ENSP00000415632.1:n.*8C=
ENST00000417972.5:c.*8C=	ENSP00000394671.1:n.*8C=
ENST00000426264.5:c.1308C=	ENSP00000389986.1:p.Asp436=
ENST00000429376.5:c.1204C=	ENSP00000410952.1:p.His402=
NM_006186.3:c.1497C=	NP_006177.1:p.Asp499=
XM_005246621.2:c.1530C=	XP_005246678.1:p.Asp510=
XM_005246622.2:c.1308C=	XP_005246679.1:p.Asp436=
XM_005246623.1:c.1308C=	XP_005246680.1:p.Asp436=
XM_006712553.2:c.1455C=	XP_006712616.1:p.Asp485=
XM_011511246.1:c.1426C=	XP_011509548.1:p.His476=
XR_427087.2:n.3582C=
NM_173173.2:c.1308C=	NP_775265.1:p.Asp436=
XM_005246621.4:c.1530C=	XP_005246678.1:p.Asp510=
XM_006712553.4:c.1455C=	XP_006712616.1:p.Asp485=
XM_011511246.2:c.1426C=	XP_011509548.1:p.His476=
XM_017004219.2:c.1497C=	XP_016859708.1:p.Asp499=
XM_017004220.2:c.1422C=	XP_016859709.1:p.Asp474=
XR_001738751.2:n.1744C=
XR_001738752.2:n.1566C=
XR_427087.4:n.1623C=
NM_006186.4:c.1497C= MANE Select	NP_006177.1:p.Asp499=
NM_173173.3:c.1308C=	NP_775265.1:p.Asp436=