Canonical Allele Identifier: CA2661538853

Gene: NR4A2

Linked Data

• gnomAD v4: 2-156325947-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325949del , CM000664.2:g.156325949del	GRCh38
NC_000002.11:g.157182461del , CM000664.1:g.157182461del	GRCh37
NC_000002.10:g.156890707del	NCBI36
NG_011821.1:g.11828del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1389del	ENSP00000514865.1:p.Ile463MetfsTer2
ENST00000700229.1:c.557del
ENST00000700230.1:c.1133del	ENSP00000514867.1:n.1133del
ENST00000700231.1:c.1518del	ENSP00000514868.1:p.Ile506MetfsTer2
ENST00000339562.9:c.1593del MANE Select	ENSP00000344479.4:p.Ile531MetfsTer2
ENST00000675870.1:c.*104del	ENSP00000502739.1:n.*104del
ENST00000339562.8:c.1593del	ENSP00000344479.4:p.Ile531MetfsTer2
ENST00000409108.6:c.1489del	ENSP00000386993.2:p.Cys497ValfsTer?
ENST00000409572.5:c.1593del	ENSP00000386747.1:p.Ile531MetfsTer2
ENST00000417764.5:c.*104del	ENSP00000415632.1:n.*104del
ENST00000417972.5:c.*104del	ENSP00000394671.1:n.*104del
ENST00000426264.5:c.1404del	ENSP00000389986.1:p.Ile468MetfsTer2
ENST00000429376.5:c.1300del	ENSP00000410952.1:p.Cys434ValfsTer?
NM_006186.3:c.1593del	NP_006177.1:p.Ile531MetfsTer2
XM_005246621.2:c.1626del	XP_005246678.1:p.Ile542MetfsTer2
XM_005246622.2:c.1404del	XP_005246679.1:p.Ile468MetfsTer2
XM_005246623.1:c.1404del	XP_005246680.1:p.Ile468MetfsTer2
XM_006712553.2:c.1551del	XP_006712616.1:p.Ile517MetfsTer2
XM_011511246.1:c.1522del	XP_011509548.1:p.Cys508ValfsTer?
NM_173173.2:c.1404del	NP_775265.1:p.Ile468MetfsTer2
XM_005246621.4:c.1626del	XP_005246678.1:p.Ile542MetfsTer2
XM_006712553.4:c.1551del	XP_006712616.1:p.Ile517MetfsTer2
XM_011511246.2:c.1522del	XP_011509548.1:p.Cys508ValfsTer?
XM_017004219.2:c.1593del	XP_016859708.1:p.Ile531MetfsTer2
XM_017004220.2:c.1518del	XP_016859709.1:p.Ile506MetfsTer2
XR_001738751.2:n.1840del
XR_001738752.2:n.1662del
XR_427087.4:n.1719del
NM_006186.4:c.1593del MANE Select	NP_006177.1:p.Ile531MetfsTer2
NM_173173.3:c.1404del	NP_775265.1:p.Ile468MetfsTer2