Canonical Allele Identifier: CA1300458990

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326119_156326120delinsAG , CM000664.2:g.156326119_156326120delinsAG	GRCh38
NC_000002.11:g.157182631_157182632delinsAG , CM000664.1:g.157182631_157182632delinsAG	GRCh37
NC_000002.10:g.156890877_156890878delinsAG	NCBI36
NG_011821.1:g.11656_11657delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1336+30_1336+31delinsCT	ENSP00000514865.1:n.1336+30_1336+31delinsCT
ENST00000700229.1:c.504+30_504+31delinsCT
ENST00000700230.1:c.1080+30_1080+31delinsCT	ENSP00000514867.1:n.1080+30_1080+31delinsCT
ENST00000700231.1:c.1465+30_1465+31delinsCT	ENSP00000514868.1:n.1465+30_1465+31delinsCT
ENST00000339562.9:c.1540+30_1540+31delinsCT MANE Select	ENSP00000344479.4:n.1540+30_1540+31delinsCT
ENST00000675870.1:c.*51+30_*51+31delinsCT	ENSP00000502739.1:n.*51+30_*51+31delinsCT
ENST00000339562.8:c.1540+30_1540+31delinsCT	ENSP00000344479.4:n.1540+30_1540+31delinsCT
ENST00000409108.6:c.1436+30_1436+31delinsCT	ENSP00000386993.2:n.1436+30_1436+31delinsCT
ENST00000409572.5:c.1540+30_1540+31delinsCT	ENSP00000386747.1:n.1540+30_1540+31delinsCT
ENST00000417764.5:c.*51+30_*51+31delinsCT	ENSP00000415632.1:n.*51+30_*51+31delinsCT
ENST00000417972.5:c.*51+30_*51+31delinsCT	ENSP00000394671.1:n.*51+30_*51+31delinsCT
ENST00000426264.5:c.1351+30_1351+31delinsCT	ENSP00000389986.1:n.1351+30_1351+31delinsCT
ENST00000429376.5:c.1247+30_1247+31delinsCT	ENSP00000410952.1:n.1247+30_1247+31delinsCT
NM_006186.3:c.1540+30_1540+31delinsCT	NP_006177.1:n.1540+30_1540+31delinsCT
XM_005246621.2:c.1573+30_1573+31delinsCT	XP_005246678.1:n.1573+30_1573+31delinsCT
XM_005246622.2:c.1351+30_1351+31delinsCT	XP_005246679.1:n.1351+30_1351+31delinsCT
XM_005246623.1:c.1351+30_1351+31delinsCT	XP_005246680.1:n.1351+30_1351+31delinsCT
XM_006712553.2:c.1498+30_1498+31delinsCT	XP_006712616.1:n.1498+30_1498+31delinsCT
XM_011511246.1:c.1469+30_1469+31delinsCT	XP_011509548.1:n.1469+30_1469+31delinsCT
XR_427087.2:n.3625+30_3625+31delinsCT
NM_173173.2:c.1351+30_1351+31delinsCT	NP_775265.1:n.1351+30_1351+31delinsCT
XM_005246621.4:c.1573+30_1573+31delinsCT	XP_005246678.1:n.1573+30_1573+31delinsCT
XM_006712553.4:c.1498+30_1498+31delinsCT	XP_006712616.1:n.1498+30_1498+31delinsCT
XM_011511246.2:c.1469+30_1469+31delinsCT	XP_011509548.1:n.1469+30_1469+31delinsCT
XM_017004219.2:c.1540+30_1540+31delinsCT	XP_016859708.1:n.1540+30_1540+31delinsCT
XM_017004220.2:c.1465+30_1465+31delinsCT	XP_016859709.1:n.1465+30_1465+31delinsCT
XR_001738751.2:n.1787+30_1787+31delinsCT
XR_001738752.2:n.1609+30_1609+31delinsCT
XR_427087.4:n.1666+30_1666+31delinsCT
NM_006186.4:c.1540+30_1540+31delinsCT MANE Select	NP_006177.1:n.1540+30_1540+31delinsCT
NM_173173.3:c.1351+30_1351+31delinsCT	NP_775265.1:n.1351+30_1351+31delinsCT