Canonical Allele Identifier: CA1300459026

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326204T= , CM000664.2:g.156326204T=	GRCh38
NC_000002.11:g.157182716T= , CM000664.1:g.157182716T=	GRCh37
NC_000002.10:g.156890962T=	NCBI36
NG_011821.1:g.11572A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1282A=	ENSP00000514865.1:p.Met428=
ENST00000700229.1:c.450A=
ENST00000700230.1:c.1026A=	ENSP00000514867.1:n.1026A=
ENST00000700231.1:c.1411A=	ENSP00000514868.1:p.Met471=
ENST00000339562.9:c.1486A= MANE Select	ENSP00000344479.4:p.Met496=
ENST00000675870.1:c.1176A=	ENSP00000502739.1:p.Ile392=
ENST00000339562.8:c.1486A=	ENSP00000344479.4:p.Met496=
ENST00000409108.6:c.1382A=	ENSP00000386993.2:p.Tyr461=
ENST00000409572.5:c.1486A=	ENSP00000386747.1:p.Met496=
ENST00000417764.5:c.1176A=	ENSP00000415632.1:p.Ile392=
ENST00000417972.5:c.1176A=	ENSP00000394671.1:p.Ile392=
ENST00000426264.5:c.1297A=	ENSP00000389986.1:p.Met433=
ENST00000429376.5:c.1193A=	ENSP00000410952.1:p.Tyr398=
NM_006186.3:c.1486A=	NP_006177.1:p.Met496=
XM_005246621.2:c.1519A=	XP_005246678.1:p.Met507=
XM_005246622.2:c.1297A=	XP_005246679.1:p.Met433=
XM_005246623.1:c.1297A=	XP_005246680.1:p.Met433=
XM_006712553.2:c.1444A=	XP_006712616.1:p.Met482=
XM_011511246.1:c.1415A=	XP_011509548.1:p.Tyr472=
XR_427087.2:n.3571A=
NM_173173.2:c.1297A=	NP_775265.1:p.Met433=
XM_005246621.4:c.1519A=	XP_005246678.1:p.Met507=
XM_006712553.4:c.1444A=	XP_006712616.1:p.Met482=
XM_011511246.2:c.1415A=	XP_011509548.1:p.Tyr472=
XM_017004219.2:c.1486A=	XP_016859708.1:p.Met496=
XM_017004220.2:c.1411A=	XP_016859709.1:p.Met471=
XR_001738751.2:n.1733A=
XR_001738752.2:n.1555A=
XR_427087.4:n.1612A=
NM_006186.4:c.1486A= MANE Select	NP_006177.1:p.Met496=
NM_173173.3:c.1297A=	NP_775265.1:p.Met433=