Canonical Allele Identifier: CA348679838

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182485C>G (hg19) ; chr2:g.156325973C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325973C>G , CM000664.2:g.156325973C>G	GRCh38
NC_000002.11:g.157182485C>G , CM000664.1:g.157182485C>G	GRCh37
NC_000002.10:g.156890731C>G	NCBI36
NG_011821.1:g.11803G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1364G>C	ENSP00000514865.1:p.Arg455Thr
ENST00000700229.1:c.532G>C
ENST00000700230.1:c.1108G>C	ENSP00000514867.1:n.1108G>C
ENST00000700231.1:c.1493G>C	ENSP00000514868.1:p.Arg498Thr
ENST00000339562.9:c.1568G>C MANE Select	ENSP00000344479.4:p.Arg523Thr
ENST00000675870.1:c.*79G>C	ENSP00000502739.1:n.*79G>C
ENST00000339562.8:c.1568G>C	ENSP00000344479.4:p.Arg523Thr
ENST00000409108.6:c.1464G>C	ENSP00000386993.2:p.Glu488Asp
ENST00000409572.5:c.1568G>C	ENSP00000386747.1:p.Arg523Thr
ENST00000417764.5:c.*79G>C	ENSP00000415632.1:n.*79G>C
ENST00000417972.5:c.*79G>C	ENSP00000394671.1:n.*79G>C
ENST00000426264.5:c.1379G>C	ENSP00000389986.1:p.Arg460Thr
ENST00000429376.5:c.1275G>C	ENSP00000410952.1:p.Glu425Asp
NM_006186.3:c.1568G>C	NP_006177.1:p.Arg523Thr
XM_005246621.2:c.1601G>C	XP_005246678.1:p.Arg534Thr
XM_005246622.2:c.1379G>C	XP_005246679.1:p.Arg460Thr
XM_005246623.1:c.1379G>C	XP_005246680.1:p.Arg460Thr
XM_006712553.2:c.1526G>C	XP_006712616.1:p.Arg509Thr
XM_011511246.1:c.1497G>C	XP_011509548.1:p.Glu499Asp
XR_427087.2:n.3653G>C
NM_173173.2:c.1379G>C	NP_775265.1:p.Arg460Thr
XM_005246621.4:c.1601G>C	XP_005246678.1:p.Arg534Thr
XM_006712553.4:c.1526G>C	XP_006712616.1:p.Arg509Thr
XM_011511246.2:c.1497G>C	XP_011509548.1:p.Glu499Asp
XM_017004219.2:c.1568G>C	XP_016859708.1:p.Arg523Thr
XM_017004220.2:c.1493G>C	XP_016859709.1:p.Arg498Thr
XR_001738751.2:n.1815G>C
XR_001738752.2:n.1637G>C
XR_427087.4:n.1694G>C
NM_006186.4:c.1568G>C MANE Select	NP_006177.1:p.Arg523Thr
NM_173173.3:c.1379G>C	NP_775265.1:p.Arg460Thr