Canonical Allele Identifier: CA1300458887

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325800A= , CM000664.2:g.156325800A=	GRCh38
NC_000002.11:g.157182312A= , CM000664.1:g.157182312A=	GRCh37
NC_000002.10:g.156890558A=	NCBI36
NG_011821.1:g.11976T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1537T=	ENSP00000514865.1:p.Leu513=
ENST00000700229.1:c.705T=
ENST00000700230.1:c.1281T=	ENSP00000514867.1:n.1281T=
ENST00000700231.1:c.1666T=	ENSP00000514868.1:p.Leu556=
ENST00000339562.9:c.1741T= MANE Select	ENSP00000344479.4:p.Leu581=
ENST00000675870.1:c.*252T=	ENSP00000502739.1:n.*252T=
ENST00000339562.8:c.1741T=	ENSP00000344479.4:p.Leu581=
ENST00000409108.6:c.1637T=	ENSP00000386993.2:p.Leu546=
ENST00000409572.5:c.1741T=	ENSP00000386747.1:p.Leu581=
ENST00000417764.5:c.*252T=	ENSP00000415632.1:n.*252T=
ENST00000417972.5:c.*252T=	ENSP00000394671.1:n.*252T=
ENST00000426264.5:c.1552T=	ENSP00000389986.1:p.Leu518=
ENST00000429376.5:c.1448T=	ENSP00000410952.1:p.Leu483=
NM_006186.3:c.1741T=	NP_006177.1:p.Leu581=
XM_005246621.2:c.1774T=	XP_005246678.1:p.Leu592=
XM_005246622.2:c.1552T=	XP_005246679.1:p.Leu518=
XM_005246623.1:c.1552T=	XP_005246680.1:p.Leu518=
XM_006712553.2:c.1699T=	XP_006712616.1:p.Leu567=
XM_011511246.1:c.1670T=	XP_011509548.1:p.Leu557=
NM_173173.2:c.1552T=	NP_775265.1:p.Leu518=
XM_005246621.4:c.1774T=	XP_005246678.1:p.Leu592=
XM_006712553.4:c.1699T=	XP_006712616.1:p.Leu567=
XM_011511246.2:c.1670T=	XP_011509548.1:p.Leu557=
XM_017004219.2:c.1741T=	XP_016859708.1:p.Leu581=
XM_017004220.2:c.1666T=	XP_016859709.1:p.Leu556=
XR_001738751.2:n.1988T=
XR_001738752.2:n.1810T=
XR_427087.4:n.1867T=
NM_006186.4:c.1741T= MANE Select	NP_006177.1:p.Leu581=
NM_173173.3:c.1552T=	NP_775265.1:p.Leu518=