Canonical Allele Identifier: CA1300458832

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325660_156325661delinsCG , CM000664.2:g.156325660_156325661delinsCG	GRCh38
NC_000002.11:g.157182172_157182173delinsCG , CM000664.1:g.157182172_157182173delinsCG	GRCh37
NC_000002.10:g.156890418_156890419delinsCG	NCBI36
NG_011821.1:g.12115_12116delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.*83_*84delinsCG	ENSP00000514865.1:n.*83_*84delinsCG
ENST00000700229.1:c.844_845delinsCG
ENST00000700230.1:c.1420_1421delinsCG	ENSP00000514867.1:n.1420_1421delinsCG
ENST00000700231.1:c.*83_*84delinsCG	ENSP00000514868.1:n.*83_*84delinsCG
ENST00000339562.9:c.*83_*84delinsCG MANE Select	ENSP00000344479.4:n.*83_*84delinsCG
ENST00000675870.1:c.*391_*392delinsCG	ENSP00000502739.1:n.*391_*392delinsCG
ENST00000339562.8:c.*83_*84delinsCG	ENSP00000344479.4:n.*83_*84delinsCG
ENST00000409572.5:c.*83_*84delinsCG	ENSP00000386747.1:n.*83_*84delinsCG
ENST00000417764.5:c.*391_*392delinsCG	ENSP00000415632.1:n.*391_*392delinsCG
ENST00000417972.5:c.*391_*392delinsCG	ENSP00000394671.1:n.*391_*392delinsCG
ENST00000426264.5:c.*83_*84delinsCG	ENSP00000389986.1:n.*83_*84delinsCG
NM_006186.3:c.*83_*84delinsCG	NP_006177.1:n.*83_*84delinsCG
XM_005246621.2:c.*83_*84delinsCG	XP_005246678.1:n.*83_*84delinsCG
XM_005246622.2:c.*83_*84delinsCG	XP_005246679.1:n.*83_*84delinsCG
XM_005246623.1:c.*83_*84delinsCG	XP_005246680.1:n.*83_*84delinsCG
XM_006712553.2:c.*83_*84delinsCG	XP_006712616.1:n.*83_*84delinsCG
XM_011511246.1:c.*114_*115delinsCG	XP_011509548.1:n.*114_*115delinsCG
NM_173173.2:c.*83_*84delinsCG	NP_775265.1:n.*83_*84delinsCG
XM_005246621.4:c.*83_*84delinsCG	XP_005246678.1:n.*83_*84delinsCG
XM_006712553.4:c.*83_*84delinsCG	XP_006712616.1:n.*83_*84delinsCG
XM_011511246.2:c.*114_*115delinsCG	XP_011509548.1:n.*114_*115delinsCG
XM_017004219.2:c.*83_*84delinsCG	XP_016859708.1:n.*83_*84delinsCG
XM_017004220.2:c.*83_*84delinsCG	XP_016859709.1:n.*83_*84delinsCG
XR_001738751.2:n.2127_2128delinsCG
XR_001738752.2:n.1949_1950delinsCG
XR_427087.4:n.2006_2007delinsCG
NM_006186.4:c.*83_*84delinsCG MANE Select	NP_006177.1:n.*83_*84delinsCG
NM_173173.3:c.*83_*84delinsCG	NP_775265.1:n.*83_*84delinsCG