Canonical Allele Identifier: CA1300460433

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329426C= , CM000664.2:g.156329426C=	GRCh38
NC_000002.11:g.157185938C= , CM000664.1:g.157185938C=	GRCh37
NC_000002.10:g.156894184C=	NCBI36
NG_011821.1:g.8350G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.632G=	ENSP00000514865.1:p.Arg211=
ENST00000700230.1:c.194G=	ENSP00000514867.1:p.Arg65=
ENST00000700231.1:c.761G=	ENSP00000514868.1:p.Arg254=
ENST00000339562.9:c.761G= MANE Select	ENSP00000344479.4:p.Arg254=
ENST00000675870.1:c.572G=	ENSP00000502739.1:p.Arg191=
ENST00000339562.8:c.761G=	ENSP00000344479.4:p.Arg254=
ENST00000406048.2:c.208+488G=
ENST00000409108.6:c.761G=	ENSP00000386993.2:p.Arg254=
ENST00000409572.5:c.761G=	ENSP00000386747.1:p.Arg254=
ENST00000417764.5:c.572G=	ENSP00000415632.1:p.Arg191=
ENST00000417972.5:c.572G=	ENSP00000394671.1:p.Arg191=
ENST00000424077.1:c.761G=	ENSP00000406808.1:p.Arg254=
ENST00000426264.5:c.572G=	ENSP00000389986.1:p.Arg191=
ENST00000429376.5:c.572G=	ENSP00000410952.1:p.Arg191=
NM_006186.3:c.761G=	NP_006177.1:p.Arg254=
XM_005246621.2:c.794G=	XP_005246678.1:p.Arg265=
XM_005246622.2:c.572G=	XP_005246679.1:p.Arg191=
XM_005246623.1:c.572G=	XP_005246680.1:p.Arg191=
XM_006712553.2:c.794G=	XP_006712616.1:p.Arg265=
XM_011511246.1:c.794G=	XP_011509548.1:p.Arg265=
XR_427087.2:n.2967G=
NM_173173.2:c.572G=	NP_775265.1:p.Arg191=
XM_005246621.4:c.794G=	XP_005246678.1:p.Arg265=
XM_006712553.4:c.794G=	XP_006712616.1:p.Arg265=
XM_011511246.2:c.794G=	XP_011509548.1:p.Arg265=
XM_017004219.2:c.761G=	XP_016859708.1:p.Arg254=
XM_017004220.2:c.761G=	XP_016859709.1:p.Arg254=
XR_001738751.2:n.1129G=
XR_001738752.2:n.951G=
XR_427087.4:n.1008G=
NM_006186.4:c.761G= MANE Select	NP_006177.1:p.Arg254=
NM_173173.3:c.572G=	NP_775265.1:p.Arg191=