Canonical Allele Identifier: CA348679343

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182305G>T (hg19) ; chr2:g.156325793G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325793G>T , CM000664.2:g.156325793G>T	GRCh38
NC_000002.11:g.157182305G>T , CM000664.1:g.157182305G>T	GRCh37
NC_000002.10:g.156890551G>T	NCBI36
NG_011821.1:g.11983C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1544C>A	ENSP00000514865.1:p.Pro515Gln
ENST00000700229.1:c.712C>A
ENST00000700230.1:c.1288C>A	ENSP00000514867.1:n.1288C>A
ENST00000700231.1:c.1673C>A	ENSP00000514868.1:p.Pro558Gln
ENST00000339562.9:c.1748C>A MANE Select	ENSP00000344479.4:p.Pro583Gln
ENST00000675870.1:c.*259C>A	ENSP00000502739.1:n.*259C>A
ENST00000339562.8:c.1748C>A	ENSP00000344479.4:p.Pro583Gln
ENST00000409108.6:c.1644C>A	ENSP00000386993.2:p.Ala548=
ENST00000409572.5:c.1748C>A	ENSP00000386747.1:p.Pro583Gln
ENST00000417764.5:c.*259C>A	ENSP00000415632.1:n.*259C>A
ENST00000417972.5:c.*259C>A	ENSP00000394671.1:n.*259C>A
ENST00000426264.5:c.1559C>A	ENSP00000389986.1:p.Pro520Gln
ENST00000429376.5:c.1455C>A	ENSP00000410952.1:p.Ala485=
NM_006186.3:c.1748C>A	NP_006177.1:p.Pro583Gln
XM_005246621.2:c.1781C>A	XP_005246678.1:p.Pro594Gln
XM_005246622.2:c.1559C>A	XP_005246679.1:p.Pro520Gln
XM_005246623.1:c.1559C>A	XP_005246680.1:p.Pro520Gln
XM_006712553.2:c.1706C>A	XP_006712616.1:p.Pro569Gln
XM_011511246.1:c.1677C>A	XP_011509548.1:p.Ala559=
NM_173173.2:c.1559C>A	NP_775265.1:p.Pro520Gln
XM_005246621.4:c.1781C>A	XP_005246678.1:p.Pro594Gln
XM_006712553.4:c.1706C>A	XP_006712616.1:p.Pro569Gln
XM_011511246.2:c.1677C>A	XP_011509548.1:p.Ala559=
XM_017004219.2:c.1748C>A	XP_016859708.1:p.Pro583Gln
XM_017004220.2:c.1673C>A	XP_016859709.1:p.Pro558Gln
XR_001738751.2:n.1995C>A
XR_001738752.2:n.1817C>A
XR_427087.4:n.1874C>A
NM_006186.4:c.1748C>A MANE Select	NP_006177.1:p.Pro583Gln
NM_173173.3:c.1559C>A	NP_775265.1:p.Pro520Gln