Canonical Allele Identifier: CA2832542900

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325911dup , CM000664.2:g.156325911dup	GRCh38
NC_000002.11:g.157182423dup , CM000664.1:g.157182423dup	GRCh37
NC_000002.10:g.156890669dup	NCBI36
NG_011821.1:g.11870dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1431dup	ENSP00000514865.1:p.Leu478ValfsTer?
ENST00000700229.1:c.599dup
ENST00000700230.1:c.1175dup	ENSP00000514867.1:n.1175dup
ENST00000700231.1:c.1560dup	ENSP00000514868.1:p.Leu521ValfsTer?
ENST00000339562.9:c.1635dup MANE Select	ENSP00000344479.4:p.Leu546ValfsTer?
ENST00000675870.1:c.*146dup	ENSP00000502739.1:n.*146dup
ENST00000339562.8:c.1635dup	ENSP00000344479.4:p.Leu546ValfsTer?
ENST00000409108.6:c.1531dup	ENSP00000386993.2:p.Val511GlyfsTer2
ENST00000409572.5:c.1635dup	ENSP00000386747.1:p.Leu546ValfsTer?
ENST00000417764.5:c.*146dup	ENSP00000415632.1:n.*146dup
ENST00000417972.5:c.*146dup	ENSP00000394671.1:n.*146dup
ENST00000426264.5:c.1446dup	ENSP00000389986.1:p.Leu483ValfsTer?
ENST00000429376.5:c.1342dup	ENSP00000410952.1:p.Val448GlyfsTer2
NM_006186.3:c.1635dup	NP_006177.1:p.Leu546ValfsTer?
XM_005246621.2:c.1668dup	XP_005246678.1:p.Leu557ValfsTer?
XM_005246622.2:c.1446dup	XP_005246679.1:p.Leu483ValfsTer?
XM_005246623.1:c.1446dup	XP_005246680.1:p.Leu483ValfsTer?
XM_006712553.2:c.1593dup	XP_006712616.1:p.Leu532ValfsTer?
XM_011511246.1:c.1564dup	XP_011509548.1:p.Val522GlyfsTer2
NM_173173.2:c.1446dup	NP_775265.1:p.Leu483ValfsTer?
XM_005246621.4:c.1668dup	XP_005246678.1:p.Leu557ValfsTer?
XM_006712553.4:c.1593dup	XP_006712616.1:p.Leu532ValfsTer?
XM_011511246.2:c.1564dup	XP_011509548.1:p.Val522GlyfsTer2
XM_017004219.2:c.1635dup	XP_016859708.1:p.Leu546ValfsTer?
XM_017004220.2:c.1560dup	XP_016859709.1:p.Leu521ValfsTer?
XR_001738751.2:n.1882dup
XR_001738752.2:n.1704dup
XR_427087.4:n.1761dup
NM_006186.4:c.1635dup MANE Select	NP_006177.1:p.Leu546ValfsTer?
NM_173173.3:c.1446dup	NP_775265.1:p.Leu483ValfsTer?