Canonical Allele Identifier: CA1300459005

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326158A= , CM000664.2:g.156326158A=	GRCh38
NC_000002.11:g.157182670A= , CM000664.1:g.157182670A=	GRCh37
NC_000002.10:g.156890916A=	NCBI36
NG_011821.1:g.11618T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1328T=	ENSP00000514865.1:p.Met443=
ENST00000700229.1:c.496T=
ENST00000700230.1:c.1072T=	ENSP00000514867.1:n.1072T=
ENST00000700231.1:c.1457T=	ENSP00000514868.1:p.Met486=
ENST00000339562.9:c.1532T= MANE Select	ENSP00000344479.4:p.Met511=
ENST00000675870.1:c.*43T=	ENSP00000502739.1:n.*43T=
ENST00000339562.8:c.1532T=	ENSP00000344479.4:p.Met511=
ENST00000409108.6:c.1428T=	ENSP00000386993.2:p.Tyr476=
ENST00000409572.5:c.1532T=	ENSP00000386747.1:p.Met511=
ENST00000417764.5:c.*43T=	ENSP00000415632.1:n.*43T=
ENST00000417972.5:c.*43T=	ENSP00000394671.1:n.*43T=
ENST00000426264.5:c.1343T=	ENSP00000389986.1:p.Met448=
ENST00000429376.5:c.1239T=	ENSP00000410952.1:p.Tyr413=
NM_006186.3:c.1532T=	NP_006177.1:p.Met511=
XM_005246621.2:c.1565T=	XP_005246678.1:p.Met522=
XM_005246622.2:c.1343T=	XP_005246679.1:p.Met448=
XM_005246623.1:c.1343T=	XP_005246680.1:p.Met448=
XM_006712553.2:c.1490T=	XP_006712616.1:p.Met497=
XM_011511246.1:c.1461T=	XP_011509548.1:p.Tyr487=
XR_427087.2:n.3617T=
NM_173173.2:c.1343T=	NP_775265.1:p.Met448=
XM_005246621.4:c.1565T=	XP_005246678.1:p.Met522=
XM_006712553.4:c.1490T=	XP_006712616.1:p.Met497=
XM_011511246.2:c.1461T=	XP_011509548.1:p.Tyr487=
XM_017004219.2:c.1532T=	XP_016859708.1:p.Met511=
XM_017004220.2:c.1457T=	XP_016859709.1:p.Met486=
XR_001738751.2:n.1779T=
XR_001738752.2:n.1601T=
XR_427087.4:n.1658T=
NM_006186.4:c.1532T= MANE Select	NP_006177.1:p.Met511=
NM_173173.3:c.1343T=	NP_775265.1:p.Met448=