Canonical Allele Identifier: CA1300459014

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326184G= , CM000664.2:g.156326184G=	GRCh38
NC_000002.11:g.157182696G= , CM000664.1:g.157182696G=	GRCh37
NC_000002.10:g.156890942G=	NCBI36
NG_011821.1:g.11592C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1302C=	ENSP00000514865.1:p.Ala434=
ENST00000700229.1:c.470C=
ENST00000700230.1:c.1046C=	ENSP00000514867.1:n.1046C=
ENST00000700231.1:c.1431C=	ENSP00000514868.1:p.Ala477=
ENST00000339562.9:c.1506C= MANE Select	ENSP00000344479.4:p.Ala502=
ENST00000675870.1:c.*17C=	ENSP00000502739.1:n.*17C=
ENST00000339562.8:c.1506C=	ENSP00000344479.4:p.Ala502=
ENST00000409108.6:c.1402C=	ENSP00000386993.2:p.Leu468=
ENST00000409572.5:c.1506C=	ENSP00000386747.1:p.Ala502=
ENST00000417764.5:c.*17C=	ENSP00000415632.1:n.*17C=
ENST00000417972.5:c.*17C=	ENSP00000394671.1:n.*17C=
ENST00000426264.5:c.1317C=	ENSP00000389986.1:p.Ala439=
ENST00000429376.5:c.1213C=	ENSP00000410952.1:p.Leu405=
NM_006186.3:c.1506C=	NP_006177.1:p.Ala502=
XM_005246621.2:c.1539C=	XP_005246678.1:p.Ala513=
XM_005246622.2:c.1317C=	XP_005246679.1:p.Ala439=
XM_005246623.1:c.1317C=	XP_005246680.1:p.Ala439=
XM_006712553.2:c.1464C=	XP_006712616.1:p.Ala488=
XM_011511246.1:c.1435C=	XP_011509548.1:p.Leu479=
XR_427087.2:n.3591C=
NM_173173.2:c.1317C=	NP_775265.1:p.Ala439=
XM_005246621.4:c.1539C=	XP_005246678.1:p.Ala513=
XM_006712553.4:c.1464C=	XP_006712616.1:p.Ala488=
XM_011511246.2:c.1435C=	XP_011509548.1:p.Leu479=
XM_017004219.2:c.1506C=	XP_016859708.1:p.Ala502=
XM_017004220.2:c.1431C=	XP_016859709.1:p.Ala477=
XR_001738751.2:n.1753C=
XR_001738752.2:n.1575C=
XR_427087.4:n.1632C=
NM_006186.4:c.1506C= MANE Select	NP_006177.1:p.Ala502=
NM_173173.3:c.1317C=	NP_775265.1:p.Ala439=