Canonical Allele Identifier: CA1300460439

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329442G= , CM000664.2:g.156329442G=	GRCh38
NC_000002.11:g.157185954G= , CM000664.1:g.157185954G=	GRCh37
NC_000002.10:g.156894200G=	NCBI36
NG_011821.1:g.8334C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.616C=	ENSP00000514865.1:p.Pro206=
ENST00000700230.1:c.178C=	ENSP00000514867.1:p.Pro60=
ENST00000700231.1:c.745C=	ENSP00000514868.1:p.Pro249=
ENST00000339562.9:c.745C= MANE Select	ENSP00000344479.4:p.Pro249=
ENST00000675870.1:c.556C=	ENSP00000502739.1:p.Pro186=
ENST00000339562.8:c.745C=	ENSP00000344479.4:p.Pro249=
ENST00000406048.2:c.208+472C=
ENST00000409108.6:c.745C=	ENSP00000386993.2:p.Pro249=
ENST00000409572.5:c.745C=	ENSP00000386747.1:p.Pro249=
ENST00000417764.5:c.556C=	ENSP00000415632.1:p.Pro186=
ENST00000417972.5:c.556C=	ENSP00000394671.1:p.Pro186=
ENST00000424077.1:c.745C=	ENSP00000406808.1:p.Pro249=
ENST00000426264.5:c.556C=	ENSP00000389986.1:p.Pro186=
ENST00000429376.5:c.556C=	ENSP00000410952.1:p.Pro186=
NM_006186.3:c.745C=	NP_006177.1:p.Pro249=
XM_005246621.2:c.778C=	XP_005246678.1:p.Pro260=
XM_005246622.2:c.556C=	XP_005246679.1:p.Pro186=
XM_005246623.1:c.556C=	XP_005246680.1:p.Pro186=
XM_006712553.2:c.778C=	XP_006712616.1:p.Pro260=
XM_011511246.1:c.778C=	XP_011509548.1:p.Pro260=
XR_427087.2:n.2951C=
NM_173173.2:c.556C=	NP_775265.1:p.Pro186=
XM_005246621.4:c.778C=	XP_005246678.1:p.Pro260=
XM_006712553.4:c.778C=	XP_006712616.1:p.Pro260=
XM_011511246.2:c.778C=	XP_011509548.1:p.Pro260=
XM_017004219.2:c.745C=	XP_016859708.1:p.Pro249=
XM_017004220.2:c.745C=	XP_016859709.1:p.Pro249=
XR_001738751.2:n.1113C=
XR_001738752.2:n.935C=
XR_427087.4:n.992C=
NM_006186.4:c.745C= MANE Select	NP_006177.1:p.Pro249=
NM_173173.3:c.556C=	NP_775265.1:p.Pro186=