Canonical Allele Identifier: CA348679426

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182335A>C (hg19) ; chr2:g.156325823A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325823A>C , CM000664.2:g.156325823A>C	GRCh38
NC_000002.11:g.157182335A>C , CM000664.1:g.157182335A>C	GRCh37
NC_000002.10:g.156890581A>C	NCBI36
NG_011821.1:g.11953T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1514T>G	ENSP00000514865.1:p.Ile505Ser
ENST00000700229.1:c.682T>G
ENST00000700230.1:c.1258T>G	ENSP00000514867.1:n.1258T>G
ENST00000700231.1:c.1643T>G	ENSP00000514868.1:p.Ile548Ser
ENST00000339562.9:c.1718T>G MANE Select	ENSP00000344479.4:p.Ile573Ser
ENST00000675870.1:c.*229T>G	ENSP00000502739.1:n.*229T>G
ENST00000339562.8:c.1718T>G	ENSP00000344479.4:p.Ile573Ser
ENST00000409108.6:c.1614T>G	ENSP00000386993.2:p.His538Gln
ENST00000409572.5:c.1718T>G	ENSP00000386747.1:p.Ile573Ser
ENST00000417764.5:c.*229T>G	ENSP00000415632.1:n.*229T>G
ENST00000417972.5:c.*229T>G	ENSP00000394671.1:n.*229T>G
ENST00000426264.5:c.1529T>G	ENSP00000389986.1:p.Ile510Ser
ENST00000429376.5:c.1425T>G	ENSP00000410952.1:p.His475Gln
NM_006186.3:c.1718T>G	NP_006177.1:p.Ile573Ser
XM_005246621.2:c.1751T>G	XP_005246678.1:p.Ile584Ser
XM_005246622.2:c.1529T>G	XP_005246679.1:p.Ile510Ser
XM_005246623.1:c.1529T>G	XP_005246680.1:p.Ile510Ser
XM_006712553.2:c.1676T>G	XP_006712616.1:p.Ile559Ser
XM_011511246.1:c.1647T>G	XP_011509548.1:p.His549Gln
NM_173173.2:c.1529T>G	NP_775265.1:p.Ile510Ser
XM_005246621.4:c.1751T>G	XP_005246678.1:p.Ile584Ser
XM_006712553.4:c.1676T>G	XP_006712616.1:p.Ile559Ser
XM_011511246.2:c.1647T>G	XP_011509548.1:p.His549Gln
XM_017004219.2:c.1718T>G	XP_016859708.1:p.Ile573Ser
XM_017004220.2:c.1643T>G	XP_016859709.1:p.Ile548Ser
XR_001738751.2:n.1965T>G
XR_001738752.2:n.1787T>G
XR_427087.4:n.1844T>G
NM_006186.4:c.1718T>G MANE Select	NP_006177.1:p.Ile573Ser
NM_173173.3:c.1529T>G	NP_775265.1:p.Ile510Ser