Canonical Allele Identifier: CA348680064

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182713T>G (hg19) ; chr2:g.156326201T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326201T>G , CM000664.2:g.156326201T>G	GRCh38
NC_000002.11:g.157182713T>G , CM000664.1:g.157182713T>G	GRCh37
NC_000002.10:g.156890959T>G	NCBI36
NG_011821.1:g.11575A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1285A>C	ENSP00000514865.1:p.Asn429His
ENST00000700229.1:c.453A>C
ENST00000700230.1:c.1029A>C	ENSP00000514867.1:n.1029A>C
ENST00000700231.1:c.1414A>C	ENSP00000514868.1:p.Asn472His
ENST00000339562.9:c.1489A>C MANE Select	ENSP00000344479.4:p.Asn497His
ENST00000675870.1:c.1179A>C	ENSP00000502739.1:p.Ter393Cys
ENST00000339562.8:c.1489A>C	ENSP00000344479.4:p.Asn497His
ENST00000409108.6:c.1385A>C	ENSP00000386993.2:p.Glu462Ala
ENST00000409572.5:c.1489A>C	ENSP00000386747.1:p.Asn497His
ENST00000417764.5:c.1179A>C	ENSP00000415632.1:p.Ter393Cys
ENST00000417972.5:c.1179A>C	ENSP00000394671.1:p.Ter393Cys
ENST00000426264.5:c.1300A>C	ENSP00000389986.1:p.Asn434His
ENST00000429376.5:c.1196A>C	ENSP00000410952.1:p.Glu399Ala
NM_006186.3:c.1489A>C	NP_006177.1:p.Asn497His
XM_005246621.2:c.1522A>C	XP_005246678.1:p.Asn508His
XM_005246622.2:c.1300A>C	XP_005246679.1:p.Asn434His
XM_005246623.1:c.1300A>C	XP_005246680.1:p.Asn434His
XM_006712553.2:c.1447A>C	XP_006712616.1:p.Asn483His
XM_011511246.1:c.1418A>C	XP_011509548.1:p.Glu473Ala
XR_427087.2:n.3574A>C
NM_173173.2:c.1300A>C	NP_775265.1:p.Asn434His
XM_005246621.4:c.1522A>C	XP_005246678.1:p.Asn508His
XM_006712553.4:c.1447A>C	XP_006712616.1:p.Asn483His
XM_011511246.2:c.1418A>C	XP_011509548.1:p.Glu473Ala
XM_017004219.2:c.1489A>C	XP_016859708.1:p.Asn497His
XM_017004220.2:c.1414A>C	XP_016859709.1:p.Asn472His
XR_001738751.2:n.1736A>C
XR_001738752.2:n.1558A>C
XR_427087.4:n.1615A>C
NM_006186.4:c.1489A>C MANE Select	NP_006177.1:p.Asn497His
NM_173173.3:c.1300A>C	NP_775265.1:p.Asn434His