Canonical Allele Identifier: CA1300460578

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329733A= , CM000664.2:g.156329733A=	GRCh38
NC_000002.11:g.157186245A= , CM000664.1:g.157186245A=	GRCh37
NC_000002.10:g.156894491A=	NCBI36
NG_011821.1:g.8043T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.265T=	ENSP00000388120.2:p.Phe89=
ENST00000700228.1:c.325T=	ENSP00000514865.1:p.Phe109=
ENST00000700231.1:c.454T=	ENSP00000514868.1:p.Phe152=
ENST00000339562.9:c.454T= MANE Select	ENSP00000344479.4:p.Phe152=
ENST00000675870.1:c.265T=	ENSP00000502739.1:p.Phe89=
ENST00000339562.8:c.454T=	ENSP00000344479.4:p.Phe152=
ENST00000406048.2:c.208+181T=
ENST00000409108.6:c.454T=	ENSP00000386993.2:p.Phe152=
ENST00000409572.5:c.454T=	ENSP00000386747.1:p.Phe152=
ENST00000417764.5:c.265T=	ENSP00000415632.1:p.Phe89=
ENST00000417972.5:c.265T=	ENSP00000394671.1:p.Phe89=
ENST00000421709.1:c.265T=	ENSP00000388120.1:p.Phe89=
ENST00000424077.1:c.454T=	ENSP00000406808.1:p.Phe152=
ENST00000426264.5:c.265T=	ENSP00000389986.1:p.Phe89=
ENST00000429376.5:c.265T=	ENSP00000410952.1:p.Phe89=
NM_006186.3:c.454T=	NP_006177.1:p.Phe152=
XM_005246621.2:c.487T=	XP_005246678.1:p.Phe163=
XM_005246622.2:c.265T=	XP_005246679.1:p.Phe89=
XM_005246623.1:c.265T=	XP_005246680.1:p.Phe89=
XM_006712553.2:c.487T=	XP_006712616.1:p.Phe163=
XM_011511246.1:c.487T=	XP_011509548.1:p.Phe163=
XR_427087.2:n.2660T=
NM_173173.2:c.265T=	NP_775265.1:p.Phe89=
XM_005246621.4:c.487T=	XP_005246678.1:p.Phe163=
XM_006712553.4:c.487T=	XP_006712616.1:p.Phe163=
XM_011511246.2:c.487T=	XP_011509548.1:p.Phe163=
XM_017004219.2:c.454T=	XP_016859708.1:p.Phe152=
XM_017004220.2:c.454T=	XP_016859709.1:p.Phe152=
XR_001738751.2:n.822T=
XR_001738752.2:n.644T=
XR_427087.4:n.701T=
NM_006186.4:c.454T= MANE Select	NP_006177.1:p.Phe152=
NM_173173.3:c.265T=	NP_775265.1:p.Phe89=