Canonical Allele Identifier: CA348679811

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325963T>G , CM000664.2:g.156325963T>G	GRCh38
NC_000002.11:g.157182475T>G , CM000664.1:g.157182475T>G	GRCh37
NC_000002.10:g.156890721T>G	NCBI36
NG_011821.1:g.11813A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006186.4:c.1578A>C MANE Select	NP_006177.1:p.Glu526Asp
ENST00000339562.9:c.1578A>C MANE Select	ENSP00000344479.4:p.Glu526Asp
NM_006186.3:c.1578A>C	NP_006177.1:p.Glu526Asp
NM_173173.2:c.1389A>C	NP_775265.1:p.Glu463Asp
NM_173173.3:c.1389A>C	NP_775265.1:p.Glu463Asp
ENST00000339562.8:c.1578A>C	ENSP00000344479.4:p.Glu526Asp
ENST00000409108.6:c.1474A>C	ENSP00000386993.2:p.Thr492Pro
ENST00000409572.5:c.1578A>C	ENSP00000386747.1:p.Glu526Asp
ENST00000417764.5:c.*89A>C	ENSP00000415632.1:n.*89A>C
ENST00000417972.5:c.*89A>C	ENSP00000394671.1:n.*89A>C
ENST00000426264.5:c.1389A>C	ENSP00000389986.1:p.Glu463Asp
ENST00000429376.5:c.1285A>C	ENSP00000410952.1:p.Thr429Pro
ENST00000675870.1:c.*89A>C	ENSP00000502739.1:n.*89A>C
ENST00000700228.1:c.1374A>C	ENSP00000514865.1:p.Glu458Asp
ENST00000700229.1:c.542A>C
ENST00000700230.1:c.1118A>C	ENSP00000514867.1:n.1118A>C
ENST00000700231.1:c.1503A>C	ENSP00000514868.1:p.Glu501Asp
XM_005246621.2:c.1611A>C	XP_005246678.1:p.Glu537Asp
XM_005246621.4:c.1611A>C	XP_005246678.1:p.Glu537Asp
XM_005246622.2:c.1389A>C	XP_005246679.1:p.Glu463Asp
XM_005246623.1:c.1389A>C	XP_005246680.1:p.Glu463Asp
XM_006712553.2:c.1536A>C	XP_006712616.1:p.Glu512Asp
XM_006712553.4:c.1536A>C	XP_006712616.1:p.Glu512Asp
XM_011511246.1:c.1507A>C	XP_011509548.1:p.Thr503Pro
XM_011511246.2:c.1507A>C	XP_011509548.1:p.Thr503Pro
XM_017004219.2:c.1578A>C	XP_016859708.1:p.Glu526Asp
XM_017004220.2:c.1503A>C	XP_016859709.1:p.Glu501Asp
XR_001738751.2:n.1825A>C
XR_001738752.2:n.1647A>C
XR_427087.4:n.1704A>C