Canonical Allele Identifier: CA1300458854

Gene: NR4A2

Linked Data

• dbSNP Id: rs1194516616

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325703_156325704insTGTTGATAACTGGAATGACA , CM000664.2:g.156325703_156325704insTGTTGATAACTGGAATGACA	GRCh38
NC_000002.11:g.157182215_157182216insTGTTGATAACTGGAATGACA , CM000664.1:g.157182215_157182216insTGTTGATAACTGGAATGACA	GRCh37
NC_000002.10:g.156890461_156890462insTGTTGATAACTGGAATGACA	NCBI36
NG_011821.1:g.12072_12073insTGTCATTCCAGTTATCAACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.*40_*41insTGTCATTCCAGTTATCAACA	ENSP00000514865.1:n.*40_*41insTGTCATTCCAGTTATCAACA
ENST00000700229.1:c.801_802insTGTCATTCCAGTTATCAACA
ENST00000700230.1:c.1377_1378insTGTCATTCCAGTTATCAACA	ENSP00000514867.1:n.1377_1378insTGTCATTCCAGTTATCAACA
ENST00000700231.1:c.*40_*41insTGTCATTCCAGTTATCAACA	ENSP00000514868.1:n.*40_*41insTGTCATTCCAGTTATCAACA
ENST00000339562.9:c.*40_*41insTGTCATTCCAGTTATCAACA MANE Select	ENSP00000344479.4:n.*40_*41insTGTCATTCCAGTTATCAACA
ENST00000675870.1:c.*348_*349insTGTCATTCCAGTTATCAACA	ENSP00000502739.1:n.*348_*349insTGTCATTCCAGTTATCAACA
ENST00000339562.8:c.*40_*41insTGTCATTCCAGTTATCAACA	ENSP00000344479.4:n.*40_*41insTGTCATTCCAGTTATCAACA
ENST00000409572.5:c.*40_*41insTGTCATTCCAGTTATCAACA	ENSP00000386747.1:n.*40_*41insTGTCATTCCAGTTATCAACA
ENST00000417764.5:c.*348_*349insTGTCATTCCAGTTATCAACA	ENSP00000415632.1:n.*348_*349insTGTCATTCCAGTTATCAACA
ENST00000417972.5:c.*348_*349insTGTCATTCCAGTTATCAACA	ENSP00000394671.1:n.*348_*349insTGTCATTCCAGTTATCAACA
ENST00000426264.5:c.*40_*41insTGTCATTCCAGTTATCAACA	ENSP00000389986.1:n.*40_*41insTGTCATTCCAGTTATCAACA
NM_006186.3:c.*40_*41insTGTCATTCCAGTTATCAACA	NP_006177.1:n.*40_*41insTGTCATTCCAGTTATCAACA
XM_005246621.2:c.*40_*41insTGTCATTCCAGTTATCAACA	XP_005246678.1:n.*40_*41insTGTCATTCCAGTTATCAACA
XM_005246622.2:c.*40_*41insTGTCATTCCAGTTATCAACA	XP_005246679.1:n.*40_*41insTGTCATTCCAGTTATCAACA
XM_005246623.1:c.*40_*41insTGTCATTCCAGTTATCAACA	XP_005246680.1:n.*40_*41insTGTCATTCCAGTTATCAACA
XM_006712553.2:c.*40_*41insTGTCATTCCAGTTATCAACA	XP_006712616.1:n.*40_*41insTGTCATTCCAGTTATCAACA
XM_011511246.1:c.*71_*72insTGTCATTCCAGTTATCAACA	XP_011509548.1:n.*71_*72insTGTCATTCCAGTTATCAACA
NM_173173.2:c.*40_*41insTGTCATTCCAGTTATCAACA	NP_775265.1:n.*40_*41insTGTCATTCCAGTTATCAACA
XM_005246621.4:c.*40_*41insTGTCATTCCAGTTATCAACA	XP_005246678.1:n.*40_*41insTGTCATTCCAGTTATCAACA
XM_006712553.4:c.*40_*41insTGTCATTCCAGTTATCAACA	XP_006712616.1:n.*40_*41insTGTCATTCCAGTTATCAACA
XM_011511246.2:c.*71_*72insTGTCATTCCAGTTATCAACA	XP_011509548.1:n.*71_*72insTGTCATTCCAGTTATCAACA
XM_017004219.2:c.*40_*41insTGTCATTCCAGTTATCAACA	XP_016859708.1:n.*40_*41insTGTCATTCCAGTTATCAACA
XM_017004220.2:c.*40_*41insTGTCATTCCAGTTATCAACA	XP_016859709.1:n.*40_*41insTGTCATTCCAGTTATCAACA
XR_001738751.2:n.2084_2085insTGTCATTCCAGTTATCAACA
XR_001738752.2:n.1906_1907insTGTCATTCCAGTTATCAACA
XR_427087.4:n.1963_1964insTGTCATTCCAGTTATCAACA
NM_006186.4:c.*40_*41insTGTCATTCCAGTTATCAACA MANE Select	NP_006177.1:n.*40_*41insTGTCATTCCAGTTATCAACA
NM_173173.3:c.*40_*41insTGTCATTCCAGTTATCAACA	NP_775265.1:n.*40_*41insTGTCATTCCAGTTATCAACA