Canonical Allele Identifier: CA429727512

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182280A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325768A>G , CM000664.2:g.156325768A>G	GRCh38
NC_000002.11:g.157182280A>G , CM000664.1:g.157182280A>G	GRCh37
NC_000002.10:g.156890526A>G	NCBI36
NG_011821.1:g.12008T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1569T>C	ENSP00000514865.1:p.Leu523=
ENST00000700229.1:c.737T>C
ENST00000700230.1:c.1313T>C	ENSP00000514867.1:n.1313T>C
ENST00000700231.1:c.1698T>C	ENSP00000514868.1:p.Leu566=
ENST00000339562.9:c.1773T>C MANE Select	ENSP00000344479.4:p.Leu591=
ENST00000675870.1:c.*284T>C	ENSP00000502739.1:n.*284T>C
ENST00000339562.8:c.1773T>C	ENSP00000344479.4:p.Leu591=
ENST00000409108.6:c.*7T>C	ENSP00000386993.2:n.*7T>C
ENST00000409572.5:c.1773T>C	ENSP00000386747.1:p.Leu591=
ENST00000417764.5:c.*284T>C	ENSP00000415632.1:n.*284T>C
ENST00000417972.5:c.*284T>C	ENSP00000394671.1:n.*284T>C
ENST00000426264.5:c.1584T>C	ENSP00000389986.1:p.Leu528=
ENST00000429376.5:c.*7T>C	ENSP00000410952.1:n.*7T>C
NM_006186.3:c.1773T>C	NP_006177.1:p.Leu591=
XM_005246621.2:c.1806T>C	XP_005246678.1:p.Leu602=
XM_005246622.2:c.1584T>C	XP_005246679.1:p.Leu528=
XM_005246623.1:c.1584T>C	XP_005246680.1:p.Leu528=
XM_006712553.2:c.1731T>C	XP_006712616.1:p.Leu577=
XM_011511246.1:c.*7T>C	XP_011509548.1:n.*7T>C
NM_173173.2:c.1584T>C	NP_775265.1:p.Leu528=
XM_005246621.4:c.1806T>C	XP_005246678.1:p.Leu602=
XM_006712553.4:c.1731T>C	XP_006712616.1:p.Leu577=
XM_011511246.2:c.*7T>C	XP_011509548.1:n.*7T>C
XM_017004219.2:c.1773T>C	XP_016859708.1:p.Leu591=
XM_017004220.2:c.1698T>C	XP_016859709.1:p.Leu566=
XR_001738751.2:n.2020T>C
XR_001738752.2:n.1842T>C
XR_427087.4:n.1899T>C
NM_006186.4:c.1773T>C MANE Select	NP_006177.1:p.Leu591=
NM_173173.3:c.1584T>C	NP_775265.1:p.Leu528=