Canonical Allele Identifier: CA348681722

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157185924T>C (hg19) ; chr2:g.156329412T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329412T>C , CM000664.2:g.156329412T>C	GRCh38
NC_000002.11:g.157185924T>C , CM000664.1:g.157185924T>C	GRCh37
NC_000002.10:g.156894170T>C	NCBI36
NG_011821.1:g.8364A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.646A>G	ENSP00000514865.1:p.Asn216Asp
ENST00000700230.1:c.208A>G	ENSP00000514867.1:p.Asn70Asp
ENST00000700231.1:c.775A>G	ENSP00000514868.1:p.Asn259Asp
ENST00000339562.9:c.775A>G MANE Select	ENSP00000344479.4:p.Asn259Asp
ENST00000675870.1:c.586A>G	ENSP00000502739.1:p.Asn196Asp
ENST00000339562.8:c.775A>G	ENSP00000344479.4:p.Asn259Asp
ENST00000406048.2:c.208+502A>G
ENST00000409108.6:c.775A>G	ENSP00000386993.2:p.Asn259Asp
ENST00000409572.5:c.775A>G	ENSP00000386747.1:p.Asn259Asp
ENST00000417764.5:c.586A>G	ENSP00000415632.1:p.Asn196Asp
ENST00000417972.5:c.586A>G	ENSP00000394671.1:p.Asn196Asp
ENST00000426264.5:c.586A>G	ENSP00000389986.1:p.Asn196Asp
ENST00000429376.5:c.586A>G	ENSP00000410952.1:p.Asn196Asp
NM_006186.3:c.775A>G	NP_006177.1:p.Asn259Asp
XM_005246621.2:c.808A>G	XP_005246678.1:p.Asn270Asp
XM_005246622.2:c.586A>G	XP_005246679.1:p.Asn196Asp
XM_005246623.1:c.586A>G	XP_005246680.1:p.Asn196Asp
XM_006712553.2:c.808A>G	XP_006712616.1:p.Asn270Asp
XM_011511246.1:c.808A>G	XP_011509548.1:p.Asn270Asp
XR_427087.2:n.2981A>G
NM_173173.2:c.586A>G	NP_775265.1:p.Asn196Asp
XM_005246621.4:c.808A>G	XP_005246678.1:p.Asn270Asp
XM_006712553.4:c.808A>G	XP_006712616.1:p.Asn270Asp
XM_011511246.2:c.808A>G	XP_011509548.1:p.Asn270Asp
XM_017004219.2:c.775A>G	XP_016859708.1:p.Asn259Asp
XM_017004220.2:c.775A>G	XP_016859709.1:p.Asn259Asp
XR_001738751.2:n.1143A>G
XR_001738752.2:n.965A>G
XR_427087.4:n.1022A>G
NM_006186.4:c.775A>G MANE Select	NP_006177.1:p.Asn259Asp
NM_173173.3:c.586A>G	NP_775265.1:p.Asn196Asp