Canonical Allele Identifier: CA429586164

Gene: NR4A2

Linked Data

• dbSNP Id: rs1686614480
• MyVariant Identifiers: chr2:g.157182271G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325759G>A , CM000664.2:g.156325759G>A	GRCh38
NC_000002.11:g.157182271G>A , CM000664.1:g.157182271G>A	GRCh37
NC_000002.10:g.156890517G>A	NCBI36
NG_011821.1:g.12017C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1578C>T	ENSP00000514865.1:p.Asp526=
ENST00000700229.1:c.746C>T
ENST00000700230.1:c.1322C>T	ENSP00000514867.1:n.1322C>T
ENST00000700231.1:c.1707C>T	ENSP00000514868.1:p.Asp569=
ENST00000339562.9:c.1782C>T MANE Select	ENSP00000344479.4:p.Asp594=
ENST00000675870.1:c.*293C>T	ENSP00000502739.1:n.*293C>T
ENST00000339562.8:c.1782C>T	ENSP00000344479.4:p.Asp594=
ENST00000409108.6:c.*16C>T	ENSP00000386993.2:n.*16C>T
ENST00000409572.5:c.1782C>T	ENSP00000386747.1:p.Asp594=
ENST00000417764.5:c.*293C>T	ENSP00000415632.1:n.*293C>T
ENST00000417972.5:c.*293C>T	ENSP00000394671.1:n.*293C>T
ENST00000426264.5:c.1593C>T	ENSP00000389986.1:p.Asp531=
ENST00000429376.5:c.*16C>T	ENSP00000410952.1:n.*16C>T
NM_006186.3:c.1782C>T	NP_006177.1:p.Asp594=
XM_005246621.2:c.1815C>T	XP_005246678.1:p.Asp605=
XM_005246622.2:c.1593C>T	XP_005246679.1:p.Asp531=
XM_005246623.1:c.1593C>T	XP_005246680.1:p.Asp531=
XM_006712553.2:c.1740C>T	XP_006712616.1:p.Asp580=
XM_011511246.1:c.*16C>T	XP_011509548.1:n.*16C>T
NM_173173.2:c.1593C>T	NP_775265.1:p.Asp531=
XM_005246621.4:c.1815C>T	XP_005246678.1:p.Asp605=
XM_006712553.4:c.1740C>T	XP_006712616.1:p.Asp580=
XM_011511246.2:c.*16C>T	XP_011509548.1:n.*16C>T
XM_017004219.2:c.1782C>T	XP_016859708.1:p.Asp594=
XM_017004220.2:c.1707C>T	XP_016859709.1:p.Asp569=
XR_001738751.2:n.2029C>T
XR_001738752.2:n.1851C>T
XR_427087.4:n.1908C>T
NM_006186.4:c.1782C>T MANE Select	NP_006177.1:p.Asp594=
NM_173173.3:c.1593C>T	NP_775265.1:p.Asp531=