Canonical Allele Identifier: CA1300458884

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325794G= , CM000664.2:g.156325794G=	GRCh38
NC_000002.11:g.157182306G= , CM000664.1:g.157182306G=	GRCh37
NC_000002.10:g.156890552G=	NCBI36
NG_011821.1:g.11982C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1543C=	ENSP00000514865.1:p.Pro515=
ENST00000700229.1:c.711C=
ENST00000700230.1:c.1287C=	ENSP00000514867.1:n.1287C=
ENST00000700231.1:c.1672C=	ENSP00000514868.1:p.Pro558=
ENST00000339562.9:c.1747C= MANE Select	ENSP00000344479.4:p.Pro583=
ENST00000675870.1:c.*258C=	ENSP00000502739.1:n.*258C=
ENST00000339562.8:c.1747C=	ENSP00000344479.4:p.Pro583=
ENST00000409108.6:c.1643C=	ENSP00000386993.2:p.Ala548=
ENST00000409572.5:c.1747C=	ENSP00000386747.1:p.Pro583=
ENST00000417764.5:c.*258C=	ENSP00000415632.1:n.*258C=
ENST00000417972.5:c.*258C=	ENSP00000394671.1:n.*258C=
ENST00000426264.5:c.1558C=	ENSP00000389986.1:p.Pro520=
ENST00000429376.5:c.1454C=	ENSP00000410952.1:p.Ala485=
NM_006186.3:c.1747C=	NP_006177.1:p.Pro583=
XM_005246621.2:c.1780C=	XP_005246678.1:p.Pro594=
XM_005246622.2:c.1558C=	XP_005246679.1:p.Pro520=
XM_005246623.1:c.1558C=	XP_005246680.1:p.Pro520=
XM_006712553.2:c.1705C=	XP_006712616.1:p.Pro569=
XM_011511246.1:c.1676C=	XP_011509548.1:p.Ala559=
NM_173173.2:c.1558C=	NP_775265.1:p.Pro520=
XM_005246621.4:c.1780C=	XP_005246678.1:p.Pro594=
XM_006712553.4:c.1705C=	XP_006712616.1:p.Pro569=
XM_011511246.2:c.1676C=	XP_011509548.1:p.Ala559=
XM_017004219.2:c.1747C=	XP_016859708.1:p.Pro583=
XM_017004220.2:c.1672C=	XP_016859709.1:p.Pro558=
XR_001738751.2:n.1994C=
XR_001738752.2:n.1816C=
XR_427087.4:n.1873C=
NM_006186.4:c.1747C= MANE Select	NP_006177.1:p.Pro583=
NM_173173.3:c.1558C=	NP_775265.1:p.Pro520=