Canonical Allele Identifier: CA2577127023

Gene: NR4A2

Linked Data

• gnomAD v4: 2-156329572-CTCCGGGTTCATGGGGACG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329574_156329591del , CM000664.2:g.156329574_156329591del	GRCh38
NC_000002.11:g.157186086_157186103del , CM000664.1:g.157186086_157186103del	GRCh37
NC_000002.10:g.156894332_156894349del	NCBI36
NG_011821.1:g.8186_8203del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.408_425del	ENSP00000388120.2:p.His136_Glu142delinsGln
ENST00000700228.1:c.468_485del	ENSP00000514865.1:p.His156_Glu162delinsGln
ENST00000700230.1:c.30_47del	ENSP00000514867.1:p.His10_Glu16delinsGln
ENST00000700231.1:c.597_614del	ENSP00000514868.1:p.His199_Glu205delinsGln
ENST00000339562.9:c.597_614del MANE Select	ENSP00000344479.4:p.His199_Glu205delinsGln
ENST00000675870.1:c.408_425del	ENSP00000502739.1:p.His136_Glu142delinsGln
ENST00000339562.8:c.597_614del	ENSP00000344479.4:p.His199_Glu205delinsGln
ENST00000406048.2:c.208+324_208+341del
ENST00000409108.6:c.597_614del	ENSP00000386993.2:p.His199_Glu205delinsGln
ENST00000409572.5:c.597_614del	ENSP00000386747.1:p.His199_Glu205delinsGln
ENST00000417764.5:c.408_425del	ENSP00000415632.1:p.His136_Glu142delinsGln
ENST00000417972.5:c.408_425del	ENSP00000394671.1:p.His136_Glu142delinsGln
ENST00000424077.1:c.597_614del	ENSP00000406808.1:p.His199_Glu205delinsGln
ENST00000426264.5:c.408_425del	ENSP00000389986.1:p.His136_Glu142delinsGln
ENST00000429376.5:c.408_425del	ENSP00000410952.1:p.His136_Glu142delinsGln
NM_006186.3:c.597_614del	NP_006177.1:p.His199_Glu205delinsGln
XM_005246621.2:c.630_647del	XP_005246678.1:p.His210_Glu216delinsGln
XM_005246622.2:c.408_425del	XP_005246679.1:p.His136_Glu142delinsGln
XM_005246623.1:c.408_425del	XP_005246680.1:p.His136_Glu142delinsGln
XM_006712553.2:c.630_647del	XP_006712616.1:p.His210_Glu216delinsGln
XM_011511246.1:c.630_647del	XP_011509548.1:p.His210_Glu216delinsGln
XR_427087.2:n.2803_2820del
NM_173173.2:c.408_425del	NP_775265.1:p.His136_Glu142delinsGln
XM_005246621.4:c.630_647del	XP_005246678.1:p.His210_Glu216delinsGln
XM_006712553.4:c.630_647del	XP_006712616.1:p.His210_Glu216delinsGln
XM_011511246.2:c.630_647del	XP_011509548.1:p.His210_Glu216delinsGln
XM_017004219.2:c.597_614del	XP_016859708.1:p.His199_Glu205delinsGln
XM_017004220.2:c.597_614del	XP_016859709.1:p.His199_Glu205delinsGln
XR_001738751.2:n.965_982del
XR_001738752.2:n.787_804del
XR_427087.4:n.844_861del
NM_006186.4:c.597_614del MANE Select	NP_006177.1:p.His199_Glu205delinsGln
NM_173173.3:c.408_425del	NP_775265.1:p.His136_Glu142delinsGln