Canonical Allele Identifier: CA1300458948

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325993G= , CM000664.2:g.156325993G=	GRCh38
NC_000002.11:g.157182505G= , CM000664.1:g.157182505G=	GRCh37
NC_000002.10:g.156890751G=	NCBI36
NG_011821.1:g.11783C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1344C=	ENSP00000514865.1:p.His448=
ENST00000700229.1:c.512C=
ENST00000700230.1:c.1088C=	ENSP00000514867.1:n.1088C=
ENST00000700231.1:c.1473C=	ENSP00000514868.1:p.His491=
ENST00000339562.9:c.1548C= MANE Select	ENSP00000344479.4:p.His516=
ENST00000675870.1:c.*59C=	ENSP00000502739.1:n.*59C=
ENST00000339562.8:c.1548C=	ENSP00000344479.4:p.His516=
ENST00000409108.6:c.1444C=	ENSP00000386993.2:p.Arg482=
ENST00000409572.5:c.1548C=	ENSP00000386747.1:p.His516=
ENST00000417764.5:c.*59C=	ENSP00000415632.1:n.*59C=
ENST00000417972.5:c.*59C=	ENSP00000394671.1:n.*59C=
ENST00000426264.5:c.1359C=	ENSP00000389986.1:p.His453=
ENST00000429376.5:c.1255C=	ENSP00000410952.1:p.Arg419=
NM_006186.3:c.1548C=	NP_006177.1:p.His516=
XM_005246621.2:c.1581C=	XP_005246678.1:p.His527=
XM_005246622.2:c.1359C=	XP_005246679.1:p.His453=
XM_005246623.1:c.1359C=	XP_005246680.1:p.His453=
XM_006712553.2:c.1506C=	XP_006712616.1:p.His502=
XM_011511246.1:c.1477C=	XP_011509548.1:p.Arg493=
XR_427087.2:n.3633C=
NM_173173.2:c.1359C=	NP_775265.1:p.His453=
XM_005246621.4:c.1581C=	XP_005246678.1:p.His527=
XM_006712553.4:c.1506C=	XP_006712616.1:p.His502=
XM_011511246.2:c.1477C=	XP_011509548.1:p.Arg493=
XM_017004219.2:c.1548C=	XP_016859708.1:p.His516=
XM_017004220.2:c.1473C=	XP_016859709.1:p.His491=
XR_001738751.2:n.1795C=
XR_001738752.2:n.1617C=
XR_427087.4:n.1674C=
NM_006186.4:c.1548C= MANE Select	NP_006177.1:p.His516=
NM_173173.3:c.1359C=	NP_775265.1:p.His453=