Canonical Allele Identifier: CA1300459009

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326169A= , CM000664.2:g.156326169A=	GRCh38
NC_000002.11:g.157182681A= , CM000664.1:g.157182681A=	GRCh37
NC_000002.10:g.156890927A=	NCBI36
NG_011821.1:g.11607T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1317T=	ENSP00000514865.1:p.Ala439=
ENST00000700229.1:c.485T=
ENST00000700230.1:c.1061T=	ENSP00000514867.1:n.1061T=
ENST00000700231.1:c.1446T=	ENSP00000514868.1:p.Ala482=
ENST00000339562.9:c.1521T= MANE Select	ENSP00000344479.4:p.Ala507=
ENST00000675870.1:c.*32T=	ENSP00000502739.1:n.*32T=
ENST00000339562.8:c.1521T=	ENSP00000344479.4:p.Ala507=
ENST00000409108.6:c.1417T=	ENSP00000386993.2:p.Cys473=
ENST00000409572.5:c.1521T=	ENSP00000386747.1:p.Ala507=
ENST00000417764.5:c.*32T=	ENSP00000415632.1:n.*32T=
ENST00000417972.5:c.*32T=	ENSP00000394671.1:n.*32T=
ENST00000426264.5:c.1332T=	ENSP00000389986.1:p.Ala444=
ENST00000429376.5:c.1228T=	ENSP00000410952.1:p.Cys410=
NM_006186.3:c.1521T=	NP_006177.1:p.Ala507=
XM_005246621.2:c.1554T=	XP_005246678.1:p.Ala518=
XM_005246622.2:c.1332T=	XP_005246679.1:p.Ala444=
XM_005246623.1:c.1332T=	XP_005246680.1:p.Ala444=
XM_006712553.2:c.1479T=	XP_006712616.1:p.Ala493=
XM_011511246.1:c.1450T=	XP_011509548.1:p.Cys484=
XR_427087.2:n.3606T=
NM_173173.2:c.1332T=	NP_775265.1:p.Ala444=
XM_005246621.4:c.1554T=	XP_005246678.1:p.Ala518=
XM_006712553.4:c.1479T=	XP_006712616.1:p.Ala493=
XM_011511246.2:c.1450T=	XP_011509548.1:p.Cys484=
XM_017004219.2:c.1521T=	XP_016859708.1:p.Ala507=
XM_017004220.2:c.1446T=	XP_016859709.1:p.Ala482=
XR_001738751.2:n.1768T=
XR_001738752.2:n.1590T=
XR_427087.4:n.1647T=
NM_006186.4:c.1521T= MANE Select	NP_006177.1:p.Ala507=
NM_173173.3:c.1332T=	NP_775265.1:p.Ala444=