Canonical Allele Identifier: CA348679864

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182494T>C (hg19) ; chr2:g.156325982T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325982T>C , CM000664.2:g.156325982T>C	GRCh38
NC_000002.11:g.157182494T>C , CM000664.1:g.157182494T>C	GRCh37
NC_000002.10:g.156890740T>C	NCBI36
NG_011821.1:g.11794A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1355A>G	ENSP00000514865.1:p.Glu452Gly
ENST00000700229.1:c.523A>G
ENST00000700230.1:c.1099A>G	ENSP00000514867.1:n.1099A>G
ENST00000700231.1:c.1484A>G	ENSP00000514868.1:p.Glu495Gly
ENST00000339562.9:c.1559A>G MANE Select	ENSP00000344479.4:p.Glu520Gly
ENST00000675870.1:c.*70A>G	ENSP00000502739.1:n.*70A>G
ENST00000339562.8:c.1559A>G	ENSP00000344479.4:p.Glu520Gly
ENST00000409108.6:c.1455A>G	ENSP00000386993.2:p.Gly485=
ENST00000409572.5:c.1559A>G	ENSP00000386747.1:p.Glu520Gly
ENST00000417764.5:c.*70A>G	ENSP00000415632.1:n.*70A>G
ENST00000417972.5:c.*70A>G	ENSP00000394671.1:n.*70A>G
ENST00000426264.5:c.1370A>G	ENSP00000389986.1:p.Glu457Gly
ENST00000429376.5:c.1266A>G	ENSP00000410952.1:p.Gly422=
NM_006186.3:c.1559A>G	NP_006177.1:p.Glu520Gly
XM_005246621.2:c.1592A>G	XP_005246678.1:p.Glu531Gly
XM_005246622.2:c.1370A>G	XP_005246679.1:p.Glu457Gly
XM_005246623.1:c.1370A>G	XP_005246680.1:p.Glu457Gly
XM_006712553.2:c.1517A>G	XP_006712616.1:p.Glu506Gly
XM_011511246.1:c.1488A>G	XP_011509548.1:p.Gly496=
XR_427087.2:n.3644A>G
NM_173173.2:c.1370A>G	NP_775265.1:p.Glu457Gly
XM_005246621.4:c.1592A>G	XP_005246678.1:p.Glu531Gly
XM_006712553.4:c.1517A>G	XP_006712616.1:p.Glu506Gly
XM_011511246.2:c.1488A>G	XP_011509548.1:p.Gly496=
XM_017004219.2:c.1559A>G	XP_016859708.1:p.Glu520Gly
XM_017004220.2:c.1484A>G	XP_016859709.1:p.Glu495Gly
XR_001738751.2:n.1806A>G
XR_001738752.2:n.1628A>G
XR_427087.4:n.1685A>G
NM_006186.4:c.1559A>G MANE Select	NP_006177.1:p.Glu520Gly
NM_173173.3:c.1370A>G	NP_775265.1:p.Glu457Gly