Canonical Allele Identifier: CA1300459013

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326180A= , CM000664.2:g.156326180A=	GRCh38
NC_000002.11:g.157182692A= , CM000664.1:g.157182692A=	GRCh37
NC_000002.10:g.156890938A=	NCBI36
NG_011821.1:g.11596T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1306T=	ENSP00000514865.1:p.Ser436=
ENST00000700229.1:c.474T=
ENST00000700230.1:c.1050T=	ENSP00000514867.1:n.1050T=
ENST00000700231.1:c.1435T=	ENSP00000514868.1:p.Ser479=
ENST00000339562.9:c.1510T= MANE Select	ENSP00000344479.4:p.Ser504=
ENST00000675870.1:c.*21T=	ENSP00000502739.1:n.*21T=
ENST00000339562.8:c.1510T=	ENSP00000344479.4:p.Ser504=
ENST00000409108.6:c.1406T=	ENSP00000386993.2:p.Leu469=
ENST00000409572.5:c.1510T=	ENSP00000386747.1:p.Ser504=
ENST00000417764.5:c.*21T=	ENSP00000415632.1:n.*21T=
ENST00000417972.5:c.*21T=	ENSP00000394671.1:n.*21T=
ENST00000426264.5:c.1321T=	ENSP00000389986.1:p.Ser441=
ENST00000429376.5:c.1217T=	ENSP00000410952.1:p.Leu406=
NM_006186.3:c.1510T=	NP_006177.1:p.Ser504=
XM_005246621.2:c.1543T=	XP_005246678.1:p.Ser515=
XM_005246622.2:c.1321T=	XP_005246679.1:p.Ser441=
XM_005246623.1:c.1321T=	XP_005246680.1:p.Ser441=
XM_006712553.2:c.1468T=	XP_006712616.1:p.Ser490=
XM_011511246.1:c.1439T=	XP_011509548.1:p.Leu480=
XR_427087.2:n.3595T=
NM_173173.2:c.1321T=	NP_775265.1:p.Ser441=
XM_005246621.4:c.1543T=	XP_005246678.1:p.Ser515=
XM_006712553.4:c.1468T=	XP_006712616.1:p.Ser490=
XM_011511246.2:c.1439T=	XP_011509548.1:p.Leu480=
XM_017004219.2:c.1510T=	XP_016859708.1:p.Ser504=
XM_017004220.2:c.1435T=	XP_016859709.1:p.Ser479=
XR_001738751.2:n.1757T=
XR_001738752.2:n.1579T=
XR_427087.4:n.1636T=
NM_006186.4:c.1510T= MANE Select	NP_006177.1:p.Ser504=
NM_173173.3:c.1321T=	NP_775265.1:p.Ser441=