Canonical Allele Identifier: CA1300458907

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325880T= , CM000664.2:g.156325880T=	GRCh38
NC_000002.11:g.157182392T= , CM000664.1:g.157182392T=	GRCh37
NC_000002.10:g.156890638T=	NCBI36
NG_011821.1:g.11896A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1457A=	ENSP00000514865.1:p.Lys486=
ENST00000700229.1:c.625A=
ENST00000700230.1:c.1201A=	ENSP00000514867.1:n.1201A=
ENST00000700231.1:c.1586A=	ENSP00000514868.1:p.Lys529=
ENST00000339562.9:c.1661A= MANE Select	ENSP00000344479.4:p.Lys554=
ENST00000675870.1:c.*172A=	ENSP00000502739.1:n.*172A=
ENST00000339562.8:c.1661A=	ENSP00000344479.4:p.Lys554=
ENST00000409108.6:c.1557A=	ENSP00000386993.2:p.Gln519=
ENST00000409572.5:c.1661A=	ENSP00000386747.1:p.Lys554=
ENST00000417764.5:c.*172A=	ENSP00000415632.1:n.*172A=
ENST00000417972.5:c.*172A=	ENSP00000394671.1:n.*172A=
ENST00000426264.5:c.1472A=	ENSP00000389986.1:p.Lys491=
ENST00000429376.5:c.1368A=	ENSP00000410952.1:p.Gln456=
NM_006186.3:c.1661A=	NP_006177.1:p.Lys554=
XM_005246621.2:c.1694A=	XP_005246678.1:p.Lys565=
XM_005246622.2:c.1472A=	XP_005246679.1:p.Lys491=
XM_005246623.1:c.1472A=	XP_005246680.1:p.Lys491=
XM_006712553.2:c.1619A=	XP_006712616.1:p.Lys540=
XM_011511246.1:c.1590A=	XP_011509548.1:p.Gln530=
NM_173173.2:c.1472A=	NP_775265.1:p.Lys491=
XM_005246621.4:c.1694A=	XP_005246678.1:p.Lys565=
XM_006712553.4:c.1619A=	XP_006712616.1:p.Lys540=
XM_011511246.2:c.1590A=	XP_011509548.1:p.Gln530=
XM_017004219.2:c.1661A=	XP_016859708.1:p.Lys554=
XM_017004220.2:c.1586A=	XP_016859709.1:p.Lys529=
XR_001738751.2:n.1908A=
XR_001738752.2:n.1730A=
XR_427087.4:n.1787A=
NM_006186.4:c.1661A= MANE Select	NP_006177.1:p.Lys554=
NM_173173.3:c.1472A=	NP_775265.1:p.Lys491=