Canonical Allele Identifier: CA348679815

Gene: NR4A2

Linked Data

• ClinVar Variation Id: 1339811
• ClinVar RCV Id: RCV001825194
• dbSNP Id: rs2105591753
• MyVariant Identifiers: chr2:g.157182477C>A (hg19) ; chr2:g.156325965C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325965C>A , CM000664.2:g.156325965C>A	GRCh38
NC_000002.11:g.157182477C>A , CM000664.1:g.157182477C>A	GRCh37
NC_000002.10:g.156890723C>A	NCBI36
NG_011821.1:g.11811G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1372G>T	ENSP00000514865.1:p.Glu458Ter
ENST00000700229.1:c.540G>T
ENST00000700230.1:c.1116G>T	ENSP00000514867.1:n.1116G>T
ENST00000700231.1:c.1501G>T	ENSP00000514868.1:p.Glu501Ter
ENST00000339562.9:c.1576G>T MANE Select	ENSP00000344479.4:p.Glu526Ter
ENST00000675870.1:c.*87G>T	ENSP00000502739.1:n.*87G>T
ENST00000339562.8:c.1576G>T	ENSP00000344479.4:p.Glu526Ter
ENST00000409108.6:c.1472G>T	ENSP00000386993.2:p.Arg491Ile
ENST00000409572.5:c.1576G>T	ENSP00000386747.1:p.Glu526Ter
ENST00000417764.5:c.*87G>T	ENSP00000415632.1:n.*87G>T
ENST00000417972.5:c.*87G>T	ENSP00000394671.1:n.*87G>T
ENST00000426264.5:c.1387G>T	ENSP00000389986.1:p.Glu463Ter
ENST00000429376.5:c.1283G>T	ENSP00000410952.1:p.Arg428Ile
NM_006186.3:c.1576G>T	NP_006177.1:p.Glu526Ter
XM_005246621.2:c.1609G>T	XP_005246678.1:p.Glu537Ter
XM_005246622.2:c.1387G>T	XP_005246679.1:p.Glu463Ter
XM_005246623.1:c.1387G>T	XP_005246680.1:p.Glu463Ter
XM_006712553.2:c.1534G>T	XP_006712616.1:p.Glu512Ter
XM_011511246.1:c.1505G>T	XP_011509548.1:p.Arg502Ile
NM_173173.2:c.1387G>T	NP_775265.1:p.Glu463Ter
XM_005246621.4:c.1609G>T	XP_005246678.1:p.Glu537Ter
XM_006712553.4:c.1534G>T	XP_006712616.1:p.Glu512Ter
XM_011511246.2:c.1505G>T	XP_011509548.1:p.Arg502Ile
XM_017004219.2:c.1576G>T	XP_016859708.1:p.Glu526Ter
XM_017004220.2:c.1501G>T	XP_016859709.1:p.Glu501Ter
XR_001738751.2:n.1823G>T
XR_001738752.2:n.1645G>T
XR_427087.4:n.1702G>T
NM_006186.4:c.1576G>T MANE Select	NP_006177.1:p.Glu526Ter
NM_173173.3:c.1387G>T	NP_775265.1:p.Glu463Ter