Canonical Allele Identifier: CA645529280

Gene: NR4A2

Linked Data

• COSMIC: COSM1641669

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329860_156329861insG , CM000664.2:g.156329860_156329861insG	GRCh38
NC_000002.11:g.157186372_157186373insG , CM000664.1:g.157186372_157186373insG	GRCh37
NC_000002.10:g.156894618_156894619insG	NCBI36
NG_011821.1:g.7915_7916insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.137_138insC	ENSP00000388120.2:p.Gln46HisfsTer3
ENST00000700228.1:c.197_198insC	ENSP00000514865.1:p.Gln66HisfsTer3
ENST00000700231.1:c.326_327insC	ENSP00000514868.1:p.Gln109HisfsTer3
ENST00000339562.9:c.326_327insC MANE Select	ENSP00000344479.4:p.Gln109HisfsTer3
ENST00000675870.1:c.137_138insC	ENSP00000502739.1:p.Gln46HisfsTer3
ENST00000339562.8:c.326_327insC	ENSP00000344479.4:p.Gln109HisfsTer3
ENST00000406048.2:c.208+53_208+54insC
ENST00000409108.6:c.326_327insC	ENSP00000386993.2:p.Gln109HisfsTer3
ENST00000409572.5:c.326_327insC	ENSP00000386747.1:p.Gln109HisfsTer3
ENST00000417764.5:c.137_138insC	ENSP00000415632.1:p.Gln46HisfsTer3
ENST00000417972.5:c.137_138insC	ENSP00000394671.1:p.Gln46HisfsTer3
ENST00000421709.1:c.137_138insC	ENSP00000388120.1:p.Gln46HisfsTer3
ENST00000424077.1:c.326_327insC	ENSP00000406808.1:p.Gln109HisfsTer3
ENST00000426264.5:c.137_138insC	ENSP00000389986.1:p.Gln46HisfsTer3
ENST00000429376.5:c.137_138insC	ENSP00000410952.1:p.Gln46HisfsTer3
NM_006186.3:c.326_327insC	NP_006177.1:p.Gln109HisfsTer3
XM_005246621.2:c.359_360insC	XP_005246678.1:p.Gln120HisfsTer3
XM_005246622.2:c.137_138insC	XP_005246679.1:p.Gln46HisfsTer3
XM_005246623.1:c.137_138insC	XP_005246680.1:p.Gln46HisfsTer3
XM_006712553.2:c.359_360insC	XP_006712616.1:p.Gln120HisfsTer3
XM_011511246.1:c.359_360insC	XP_011509548.1:p.Gln120HisfsTer3
XR_427087.2:n.2532_2533insC
NM_173173.2:c.137_138insC	NP_775265.1:p.Gln46HisfsTer3
XM_005246621.4:c.359_360insC	XP_005246678.1:p.Gln120HisfsTer3
XM_006712553.4:c.359_360insC	XP_006712616.1:p.Gln120HisfsTer3
XM_011511246.2:c.359_360insC	XP_011509548.1:p.Gln120HisfsTer3
XM_017004219.2:c.326_327insC	XP_016859708.1:p.Gln109HisfsTer3
XM_017004220.2:c.326_327insC	XP_016859709.1:p.Gln109HisfsTer3
XR_001738751.2:n.694_695insC
XR_001738752.2:n.516_517insC
XR_427087.4:n.573_574insC
NM_006186.4:c.326_327insC MANE Select	NP_006177.1:p.Gln109HisfsTer3
NM_173173.3:c.137_138insC	NP_775265.1:p.Gln46HisfsTer3