Canonical Allele Identifier: CA429727836

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157186373_157186374insC (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329861_156329862insC , CM000664.2:g.156329861_156329862insC	GRCh38
NC_000002.11:g.157186373_157186374insC , CM000664.1:g.157186373_157186374insC	GRCh37
NC_000002.10:g.156894619_156894620insC	NCBI36
NG_011821.1:g.7914_7915insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.136_137insG	ENSP00000388120.2:p.Gln46ArgfsTer3
ENST00000700228.1:c.196_197insG	ENSP00000514865.1:p.Gln66ArgfsTer3
ENST00000700231.1:c.325_326insG	ENSP00000514868.1:p.Gln109ArgfsTer3
ENST00000339562.9:c.325_326insG MANE Select	ENSP00000344479.4:p.Gln109ArgfsTer3
ENST00000675870.1:c.136_137insG	ENSP00000502739.1:p.Gln46ArgfsTer3
ENST00000339562.8:c.325_326insG	ENSP00000344479.4:p.Gln109ArgfsTer3
ENST00000406048.2:c.208+52_208+53insG
ENST00000409108.6:c.325_326insG	ENSP00000386993.2:p.Gln109ArgfsTer3
ENST00000409572.5:c.325_326insG	ENSP00000386747.1:p.Gln109ArgfsTer3
ENST00000417764.5:c.136_137insG	ENSP00000415632.1:p.Gln46ArgfsTer3
ENST00000417972.5:c.136_137insG	ENSP00000394671.1:p.Gln46ArgfsTer3
ENST00000421709.1:c.136_137insG	ENSP00000388120.1:p.Gln46ArgfsTer3
ENST00000424077.1:c.325_326insG	ENSP00000406808.1:p.Gln109ArgfsTer3
ENST00000426264.5:c.136_137insG	ENSP00000389986.1:p.Gln46ArgfsTer3
ENST00000429376.5:c.136_137insG	ENSP00000410952.1:p.Gln46ArgfsTer3
NM_006186.3:c.325_326insG	NP_006177.1:p.Gln109ArgfsTer3
XM_005246621.2:c.358_359insG	XP_005246678.1:p.Gln120ArgfsTer3
XM_005246622.2:c.136_137insG	XP_005246679.1:p.Gln46ArgfsTer3
XM_005246623.1:c.136_137insG	XP_005246680.1:p.Gln46ArgfsTer3
XM_006712553.2:c.358_359insG	XP_006712616.1:p.Gln120ArgfsTer3
XM_011511246.1:c.358_359insG	XP_011509548.1:p.Gln120ArgfsTer3
XR_427087.2:n.2531_2532insG
NM_173173.2:c.136_137insG	NP_775265.1:p.Gln46ArgfsTer3
XM_005246621.4:c.358_359insG	XP_005246678.1:p.Gln120ArgfsTer3
XM_006712553.4:c.358_359insG	XP_006712616.1:p.Gln120ArgfsTer3
XM_011511246.2:c.358_359insG	XP_011509548.1:p.Gln120ArgfsTer3
XM_017004219.2:c.325_326insG	XP_016859708.1:p.Gln109ArgfsTer3
XM_017004220.2:c.325_326insG	XP_016859709.1:p.Gln109ArgfsTer3
XR_001738751.2:n.693_694insG
XR_001738752.2:n.515_516insG
XR_427087.4:n.572_573insG
NM_006186.4:c.325_326insG MANE Select	NP_006177.1:p.Gln109ArgfsTer3
NM_173173.3:c.136_137insG	NP_775265.1:p.Gln46ArgfsTer3