Canonical Allele Identifier: CA1300460730

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156330181A= , CM000664.2:g.156330181A=	GRCh38
NC_000002.11:g.157186693A= , CM000664.1:g.157186693A=	GRCh37
NC_000002.10:g.156894939A=	NCBI36
NG_011821.1:g.7595T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.-13-171T=	ENSP00000388120.2:n.-13-171T=
ENST00000700228.1:c.-114-10T=	ENSP00000514865.1:n.-114-10T=
ENST00000700231.1:c.6T=	ENSP00000514868.1:p.Pro2=
ENST00000339562.9:c.6T= MANE Select	ENSP00000344479.4:p.Pro2=
ENST00000675870.1:c.-13-171T=	ENSP00000502739.1:n.-13-171T=
ENST00000339562.8:c.6T=	ENSP00000344479.4:p.Pro2=
ENST00000409108.6:c.6T=	ENSP00000386993.2:p.Pro2=
ENST00000409572.5:c.6T=	ENSP00000386747.1:p.Pro2=
ENST00000417764.5:c.-13-171T=	ENSP00000415632.1:n.-13-171T=
ENST00000417972.5:c.-13-171T=	ENSP00000394671.1:n.-13-171T=
ENST00000421709.1:c.-13-171T=	ENSP00000388120.1:n.-13-171T=
ENST00000424077.1:c.6T=	ENSP00000406808.1:p.Pro2=
ENST00000426264.5:c.-13-171T=	ENSP00000389986.1:n.-13-171T=
ENST00000429376.5:c.-13-171T=	ENSP00000410952.1:n.-13-171T=
NM_006186.3:c.6T=	NP_006177.1:p.Pro2=
XM_005246621.2:c.39T=	XP_005246678.1:p.Pro13=
XM_005246622.2:c.-13-171T=	XP_005246679.1:n.-13-171T=
XM_005246623.1:c.-13-171T=	XP_005246680.1:n.-13-171T=
XM_006712553.2:c.39T=	XP_006712616.1:p.Pro13=
XM_011511246.1:c.39T=	XP_011509548.1:p.Pro13=
XR_427087.2:n.2212T=
NM_173173.2:c.-13-171T=	NP_775265.1:n.-13-171T=
XM_005246621.4:c.39T=	XP_005246678.1:p.Pro13=
XM_006712553.4:c.39T=	XP_006712616.1:p.Pro13=
XM_011511246.2:c.39T=	XP_011509548.1:p.Pro13=
XM_017004219.2:c.6T=	XP_016859708.1:p.Pro2=
XM_017004220.2:c.6T=	XP_016859709.1:p.Pro2=
XR_001738751.2:n.374T=
XR_001738752.2:n.367-171T=
XR_427087.4:n.253T=
NM_006186.4:c.6T= MANE Select	NP_006177.1:p.Pro2=
NM_173173.3:c.-13-171T=	NP_775265.1:n.-13-171T=