Canonical Allele Identifier: CA1300458876

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325762C= , CM000664.2:g.156325762C=	GRCh38
NC_000002.11:g.157182274C= , CM000664.1:g.157182274C=	GRCh37
NC_000002.10:g.156890520C=	NCBI36
NG_011821.1:g.12014G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1575G=	ENSP00000514865.1:p.Leu525=
ENST00000700229.1:c.743G=
ENST00000700230.1:c.1319G=	ENSP00000514867.1:n.1319G=
ENST00000700231.1:c.1704G=	ENSP00000514868.1:p.Leu568=
ENST00000339562.9:c.1779G= MANE Select	ENSP00000344479.4:p.Leu593=
ENST00000675870.1:c.*290G=	ENSP00000502739.1:n.*290G=
ENST00000339562.8:c.1779G=	ENSP00000344479.4:p.Leu593=
ENST00000409108.6:c.*13G=	ENSP00000386993.2:n.*13G=
ENST00000409572.5:c.1779G=	ENSP00000386747.1:p.Leu593=
ENST00000417764.5:c.*290G=	ENSP00000415632.1:n.*290G=
ENST00000417972.5:c.*290G=	ENSP00000394671.1:n.*290G=
ENST00000426264.5:c.1590G=	ENSP00000389986.1:p.Leu530=
ENST00000429376.5:c.*13G=	ENSP00000410952.1:n.*13G=
NM_006186.3:c.1779G=	NP_006177.1:p.Leu593=
XM_005246621.2:c.1812G=	XP_005246678.1:p.Leu604=
XM_005246622.2:c.1590G=	XP_005246679.1:p.Leu530=
XM_005246623.1:c.1590G=	XP_005246680.1:p.Leu530=
XM_006712553.2:c.1737G=	XP_006712616.1:p.Leu579=
XM_011511246.1:c.*13G=	XP_011509548.1:n.*13G=
NM_173173.2:c.1590G=	NP_775265.1:p.Leu530=
XM_005246621.4:c.1812G=	XP_005246678.1:p.Leu604=
XM_006712553.4:c.1737G=	XP_006712616.1:p.Leu579=
XM_011511246.2:c.*13G=	XP_011509548.1:n.*13G=
XM_017004219.2:c.1779G=	XP_016859708.1:p.Leu593=
XM_017004220.2:c.1704G=	XP_016859709.1:p.Leu568=
XR_001738751.2:n.2026G=
XR_001738752.2:n.1848G=
XR_427087.4:n.1905G=
NM_006186.4:c.1779G= MANE Select	NP_006177.1:p.Leu593=
NM_173173.3:c.1590G=	NP_775265.1:p.Leu530=