Canonical Allele Identifier: CA1300460577

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329731G= , CM000664.2:g.156329731G=	GRCh38
NC_000002.11:g.157186243G= , CM000664.1:g.157186243G=	GRCh37
NC_000002.10:g.156894489G=	NCBI36
NG_011821.1:g.8045C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.267C=	ENSP00000388120.2:p.Phe89=
ENST00000700228.1:c.327C=	ENSP00000514865.1:p.Phe109=
ENST00000700231.1:c.456C=	ENSP00000514868.1:p.Phe152=
ENST00000339562.9:c.456C= MANE Select	ENSP00000344479.4:p.Phe152=
ENST00000675870.1:c.267C=	ENSP00000502739.1:p.Phe89=
ENST00000339562.8:c.456C=	ENSP00000344479.4:p.Phe152=
ENST00000406048.2:c.208+183C=
ENST00000409108.6:c.456C=	ENSP00000386993.2:p.Phe152=
ENST00000409572.5:c.456C=	ENSP00000386747.1:p.Phe152=
ENST00000417764.5:c.267C=	ENSP00000415632.1:p.Phe89=
ENST00000417972.5:c.267C=	ENSP00000394671.1:p.Phe89=
ENST00000421709.1:c.267C=	ENSP00000388120.1:p.Phe89=
ENST00000424077.1:c.456C=	ENSP00000406808.1:p.Phe152=
ENST00000426264.5:c.267C=	ENSP00000389986.1:p.Phe89=
ENST00000429376.5:c.267C=	ENSP00000410952.1:p.Phe89=
NM_006186.3:c.456C=	NP_006177.1:p.Phe152=
XM_005246621.2:c.489C=	XP_005246678.1:p.Phe163=
XM_005246622.2:c.267C=	XP_005246679.1:p.Phe89=
XM_005246623.1:c.267C=	XP_005246680.1:p.Phe89=
XM_006712553.2:c.489C=	XP_006712616.1:p.Phe163=
XM_011511246.1:c.489C=	XP_011509548.1:p.Phe163=
XR_427087.2:n.2662C=
NM_173173.2:c.267C=	NP_775265.1:p.Phe89=
XM_005246621.4:c.489C=	XP_005246678.1:p.Phe163=
XM_006712553.4:c.489C=	XP_006712616.1:p.Phe163=
XM_011511246.2:c.489C=	XP_011509548.1:p.Phe163=
XM_017004219.2:c.456C=	XP_016859708.1:p.Phe152=
XM_017004220.2:c.456C=	XP_016859709.1:p.Phe152=
XR_001738751.2:n.824C=
XR_001738752.2:n.646C=
XR_427087.4:n.703C=
NM_006186.4:c.456C= MANE Select	NP_006177.1:p.Phe152=
NM_173173.3:c.267C=	NP_775265.1:p.Phe89=