Canonical Allele Identifier: CA348679929

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182662C>G (hg19) ; chr2:g.156326150C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326150C>G , CM000664.2:g.156326150C>G	GRCh38
NC_000002.11:g.157182662C>G , CM000664.1:g.157182662C>G	GRCh37
NC_000002.10:g.156890908C>G	NCBI36
NG_011821.1:g.11626G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1336G>C	ENSP00000514865.1:p.Glu446Gln
ENST00000700229.1:c.504G>C
ENST00000700230.1:c.1080G>C	ENSP00000514867.1:n.1080G>C
ENST00000700231.1:c.1465G>C	ENSP00000514868.1:p.Glu489Gln
ENST00000339562.9:c.1540G>C MANE Select	ENSP00000344479.4:p.Glu514Gln
ENST00000675870.1:c.*51G>C	ENSP00000502739.1:n.*51G>C
ENST00000339562.8:c.1540G>C	ENSP00000344479.4:p.Glu514Gln
ENST00000409108.6:c.1436G>C	ENSP00000386993.2:p.Arg479Thr
ENST00000409572.5:c.1540G>C	ENSP00000386747.1:p.Glu514Gln
ENST00000417764.5:c.*51G>C	ENSP00000415632.1:n.*51G>C
ENST00000417972.5:c.*51G>C	ENSP00000394671.1:n.*51G>C
ENST00000426264.5:c.1351G>C	ENSP00000389986.1:p.Glu451Gln
ENST00000429376.5:c.1247G>C	ENSP00000410952.1:p.Arg416Thr
NM_006186.3:c.1540G>C	NP_006177.1:p.Glu514Gln
XM_005246621.2:c.1573G>C	XP_005246678.1:p.Glu525Gln
XM_005246622.2:c.1351G>C	XP_005246679.1:p.Glu451Gln
XM_005246623.1:c.1351G>C	XP_005246680.1:p.Glu451Gln
XM_006712553.2:c.1498G>C	XP_006712616.1:p.Glu500Gln
XM_011511246.1:c.1469G>C	XP_011509548.1:p.Arg490Thr
XR_427087.2:n.3625G>C
NM_173173.2:c.1351G>C	NP_775265.1:p.Glu451Gln
XM_005246621.4:c.1573G>C	XP_005246678.1:p.Glu525Gln
XM_006712553.4:c.1498G>C	XP_006712616.1:p.Glu500Gln
XM_011511246.2:c.1469G>C	XP_011509548.1:p.Arg490Thr
XM_017004219.2:c.1540G>C	XP_016859708.1:p.Glu514Gln
XM_017004220.2:c.1465G>C	XP_016859709.1:p.Glu489Gln
XR_001738751.2:n.1787G>C
XR_001738752.2:n.1609G>C
XR_427087.4:n.1666G>C
NM_006186.4:c.1540G>C MANE Select	NP_006177.1:p.Glu514Gln
NM_173173.3:c.1351G>C	NP_775265.1:p.Glu451Gln