Canonical Allele Identifier: CA348679708

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182440T>C (hg19) ; chr2:g.156325928T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325928T>C , CM000664.2:g.156325928T>C	GRCh38
NC_000002.11:g.157182440T>C , CM000664.1:g.157182440T>C	GRCh37
NC_000002.10:g.156890686T>C	NCBI36
NG_011821.1:g.11848A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1409A>G	ENSP00000514865.1:p.His470Arg
ENST00000700229.1:c.577A>G
ENST00000700230.1:c.1153A>G	ENSP00000514867.1:n.1153A>G
ENST00000700231.1:c.1538A>G	ENSP00000514868.1:p.His513Arg
ENST00000339562.9:c.1613A>G MANE Select	ENSP00000344479.4:p.His538Arg
ENST00000675870.1:c.*124A>G	ENSP00000502739.1:n.*124A>G
ENST00000339562.8:c.1613A>G	ENSP00000344479.4:p.His538Arg
ENST00000409108.6:c.1509A>G	ENSP00000386993.2:p.Pro503=
ENST00000409572.5:c.1613A>G	ENSP00000386747.1:p.His538Arg
ENST00000417764.5:c.*124A>G	ENSP00000415632.1:n.*124A>G
ENST00000417972.5:c.*124A>G	ENSP00000394671.1:n.*124A>G
ENST00000426264.5:c.1424A>G	ENSP00000389986.1:p.His475Arg
ENST00000429376.5:c.1320A>G	ENSP00000410952.1:p.Pro440=
NM_006186.3:c.1613A>G	NP_006177.1:p.His538Arg
XM_005246621.2:c.1646A>G	XP_005246678.1:p.His549Arg
XM_005246622.2:c.1424A>G	XP_005246679.1:p.His475Arg
XM_005246623.1:c.1424A>G	XP_005246680.1:p.His475Arg
XM_006712553.2:c.1571A>G	XP_006712616.1:p.His524Arg
XM_011511246.1:c.1542A>G	XP_011509548.1:p.Pro514=
NM_173173.2:c.1424A>G	NP_775265.1:p.His475Arg
XM_005246621.4:c.1646A>G	XP_005246678.1:p.His549Arg
XM_006712553.4:c.1571A>G	XP_006712616.1:p.His524Arg
XM_011511246.2:c.1542A>G	XP_011509548.1:p.Pro514=
XM_017004219.2:c.1613A>G	XP_016859708.1:p.His538Arg
XM_017004220.2:c.1538A>G	XP_016859709.1:p.His513Arg
XR_001738751.2:n.1860A>G
XR_001738752.2:n.1682A>G
XR_427087.4:n.1739A>G
NM_006186.4:c.1613A>G MANE Select	NP_006177.1:p.His538Arg
NM_173173.3:c.1424A>G	NP_775265.1:p.His475Arg