Canonical Allele Identifier: CA348679488

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182357A>C (hg19) ; chr2:g.156325845A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325845A>C , CM000664.2:g.156325845A>C	GRCh38
NC_000002.11:g.157182357A>C , CM000664.1:g.157182357A>C	GRCh37
NC_000002.10:g.156890603A>C	NCBI36
NG_011821.1:g.11931T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1492T>G	ENSP00000514865.1:p.Cys498Gly
ENST00000700229.1:c.660T>G
ENST00000700230.1:c.1236T>G	ENSP00000514867.1:n.1236T>G
ENST00000700231.1:c.1621T>G	ENSP00000514868.1:p.Cys541Gly
ENST00000339562.9:c.1696T>G MANE Select	ENSP00000344479.4:p.Cys566Gly
ENST00000675870.1:c.*207T>G	ENSP00000502739.1:n.*207T>G
ENST00000339562.8:c.1696T>G	ENSP00000344479.4:p.Cys566Gly
ENST00000409108.6:c.1592T>G	ENSP00000386993.2:p.Leu531Trp
ENST00000409572.5:c.1696T>G	ENSP00000386747.1:p.Cys566Gly
ENST00000417764.5:c.*207T>G	ENSP00000415632.1:n.*207T>G
ENST00000417972.5:c.*207T>G	ENSP00000394671.1:n.*207T>G
ENST00000426264.5:c.1507T>G	ENSP00000389986.1:p.Cys503Gly
ENST00000429376.5:c.1403T>G	ENSP00000410952.1:p.Leu468Trp
NM_006186.3:c.1696T>G	NP_006177.1:p.Cys566Gly
XM_005246621.2:c.1729T>G	XP_005246678.1:p.Cys577Gly
XM_005246622.2:c.1507T>G	XP_005246679.1:p.Cys503Gly
XM_005246623.1:c.1507T>G	XP_005246680.1:p.Cys503Gly
XM_006712553.2:c.1654T>G	XP_006712616.1:p.Cys552Gly
XM_011511246.1:c.1625T>G	XP_011509548.1:p.Leu542Trp
NM_173173.2:c.1507T>G	NP_775265.1:p.Cys503Gly
XM_005246621.4:c.1729T>G	XP_005246678.1:p.Cys577Gly
XM_006712553.4:c.1654T>G	XP_006712616.1:p.Cys552Gly
XM_011511246.2:c.1625T>G	XP_011509548.1:p.Leu542Trp
XM_017004219.2:c.1696T>G	XP_016859708.1:p.Cys566Gly
XM_017004220.2:c.1621T>G	XP_016859709.1:p.Cys541Gly
XR_001738751.2:n.1943T>G
XR_001738752.2:n.1765T>G
XR_427087.4:n.1822T>G
NM_006186.4:c.1696T>G MANE Select	NP_006177.1:p.Cys566Gly
NM_173173.3:c.1507T>G	NP_775265.1:p.Cys503Gly