Canonical Allele Identifier: CA2752797394

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329407del , CM000664.2:g.156329407del	GRCh38
NC_000002.11:g.157185919del , CM000664.1:g.157185919del	GRCh37
NC_000002.10:g.156894165del	NCBI36
NG_011821.1:g.8372del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.654del	ENSP00000514865.1:p.Leu219CysfsTer?
ENST00000700230.1:c.216del	ENSP00000514867.1:p.Leu73CysfsTer?
ENST00000700231.1:c.783del	ENSP00000514868.1:p.Leu262CysfsTer?
ENST00000339562.9:c.783del MANE Select	ENSP00000344479.4:p.Leu262CysfsTer?
ENST00000675870.1:c.594del	ENSP00000502739.1:p.Leu199CysfsTer?
ENST00000339562.8:c.783del	ENSP00000344479.4:p.Leu262CysfsTer?
ENST00000406048.2:c.208+510del
ENST00000409108.6:c.783del	ENSP00000386993.2:p.Leu262CysfsTer?
ENST00000409572.5:c.783del	ENSP00000386747.1:p.Leu262CysfsTer?
ENST00000417764.5:c.594del	ENSP00000415632.1:p.Leu199CysfsTer?
ENST00000417972.5:c.594del	ENSP00000394671.1:p.Leu199CysfsTer?
ENST00000426264.5:c.594del	ENSP00000389986.1:p.Leu199CysfsTer?
ENST00000429376.5:c.594del	ENSP00000410952.1:p.Leu199CysfsTer?
NM_006186.3:c.783del	NP_006177.1:p.Leu262CysfsTer?
XM_005246621.2:c.816del	XP_005246678.1:p.Leu273CysfsTer?
XM_005246622.2:c.594del	XP_005246679.1:p.Leu199CysfsTer?
XM_005246623.1:c.594del	XP_005246680.1:p.Leu199CysfsTer?
XM_006712553.2:c.816del	XP_006712616.1:p.Leu273CysfsTer?
XM_011511246.1:c.816del	XP_011509548.1:p.Leu273CysfsTer?
XR_427087.2:n.2989del
NM_173173.2:c.594del	NP_775265.1:p.Leu199CysfsTer?
XM_005246621.4:c.816del	XP_005246678.1:p.Leu273CysfsTer?
XM_006712553.4:c.816del	XP_006712616.1:p.Leu273CysfsTer?
XM_011511246.2:c.816del	XP_011509548.1:p.Leu273CysfsTer?
XM_017004219.2:c.783del	XP_016859708.1:p.Leu262CysfsTer?
XM_017004220.2:c.783del	XP_016859709.1:p.Leu262CysfsTer?
XR_001738751.2:n.1151del
XR_001738752.2:n.973del
XR_427087.4:n.1030del
NM_006186.4:c.783del MANE Select	NP_006177.1:p.Leu262CysfsTer?
NM_173173.3:c.594del	NP_775265.1:p.Leu199CysfsTer?