Canonical Allele Identifier: CA429586160

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182267A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325755A>G , CM000664.2:g.156325755A>G	GRCh38
NC_000002.11:g.157182267A>G , CM000664.1:g.157182267A>G	GRCh37
NC_000002.10:g.156890513A>G	NCBI36
NG_011821.1:g.12021T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1582T>C	ENSP00000514865.1:p.Leu528=
ENST00000700229.1:c.750T>C
ENST00000700230.1:c.1326T>C	ENSP00000514867.1:n.1326T>C
ENST00000700231.1:c.1711T>C	ENSP00000514868.1:p.Leu571=
ENST00000339562.9:c.1786T>C MANE Select	ENSP00000344479.4:p.Leu596=
ENST00000675870.1:c.*297T>C	ENSP00000502739.1:n.*297T>C
ENST00000339562.8:c.1786T>C	ENSP00000344479.4:p.Leu596=
ENST00000409108.6:c.*20T>C	ENSP00000386993.2:n.*20T>C
ENST00000409572.5:c.1786T>C	ENSP00000386747.1:p.Leu596=
ENST00000417764.5:c.*297T>C	ENSP00000415632.1:n.*297T>C
ENST00000417972.5:c.*297T>C	ENSP00000394671.1:n.*297T>C
ENST00000426264.5:c.1597T>C	ENSP00000389986.1:p.Leu533=
ENST00000429376.5:c.*20T>C	ENSP00000410952.1:n.*20T>C
NM_006186.3:c.1786T>C	NP_006177.1:p.Leu596=
XM_005246621.2:c.1819T>C	XP_005246678.1:p.Leu607=
XM_005246622.2:c.1597T>C	XP_005246679.1:p.Leu533=
XM_005246623.1:c.1597T>C	XP_005246680.1:p.Leu533=
XM_006712553.2:c.1744T>C	XP_006712616.1:p.Leu582=
XM_011511246.1:c.*20T>C	XP_011509548.1:n.*20T>C
NM_173173.2:c.1597T>C	NP_775265.1:p.Leu533=
XM_005246621.4:c.1819T>C	XP_005246678.1:p.Leu607=
XM_006712553.4:c.1744T>C	XP_006712616.1:p.Leu582=
XM_011511246.2:c.*20T>C	XP_011509548.1:n.*20T>C
XM_017004219.2:c.1786T>C	XP_016859708.1:p.Leu596=
XM_017004220.2:c.1711T>C	XP_016859709.1:p.Leu571=
XR_001738751.2:n.2033T>C
XR_001738752.2:n.1855T>C
XR_427087.4:n.1912T>C
NM_006186.4:c.1786T>C MANE Select	NP_006177.1:p.Leu596=
NM_173173.3:c.1597T>C	NP_775265.1:p.Leu533=