Canonical Allele Identifier: CA1300460426

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329413G= , CM000664.2:g.156329413G=	GRCh38
NC_000002.11:g.157185925G= , CM000664.1:g.157185925G=	GRCh37
NC_000002.10:g.156894171G=	NCBI36
NG_011821.1:g.8363C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.645C=	ENSP00000514865.1:p.Ser215=
ENST00000700230.1:c.207C=	ENSP00000514867.1:p.Ser69=
ENST00000700231.1:c.774C=	ENSP00000514868.1:p.Ser258=
ENST00000339562.9:c.774C= MANE Select	ENSP00000344479.4:p.Ser258=
ENST00000675870.1:c.585C=	ENSP00000502739.1:p.Ser195=
ENST00000339562.8:c.774C=	ENSP00000344479.4:p.Ser258=
ENST00000406048.2:c.208+501C=
ENST00000409108.6:c.774C=	ENSP00000386993.2:p.Ser258=
ENST00000409572.5:c.774C=	ENSP00000386747.1:p.Ser258=
ENST00000417764.5:c.585C=	ENSP00000415632.1:p.Ser195=
ENST00000417972.5:c.585C=	ENSP00000394671.1:p.Ser195=
ENST00000424077.1:c.774C=	ENSP00000406808.1:p.Ser258=
ENST00000426264.5:c.585C=	ENSP00000389986.1:p.Ser195=
ENST00000429376.5:c.585C=	ENSP00000410952.1:p.Ser195=
NM_006186.3:c.774C=	NP_006177.1:p.Ser258=
XM_005246621.2:c.807C=	XP_005246678.1:p.Ser269=
XM_005246622.2:c.585C=	XP_005246679.1:p.Ser195=
XM_005246623.1:c.585C=	XP_005246680.1:p.Ser195=
XM_006712553.2:c.807C=	XP_006712616.1:p.Ser269=
XM_011511246.1:c.807C=	XP_011509548.1:p.Ser269=
XR_427087.2:n.2980C=
NM_173173.2:c.585C=	NP_775265.1:p.Ser195=
XM_005246621.4:c.807C=	XP_005246678.1:p.Ser269=
XM_006712553.4:c.807C=	XP_006712616.1:p.Ser269=
XM_011511246.2:c.807C=	XP_011509548.1:p.Ser269=
XM_017004219.2:c.774C=	XP_016859708.1:p.Ser258=
XM_017004220.2:c.774C=	XP_016859709.1:p.Ser258=
XR_001738751.2:n.1142C=
XR_001738752.2:n.964C=
XR_427087.4:n.1021C=
NM_006186.4:c.774C= MANE Select	NP_006177.1:p.Ser258=
NM_173173.3:c.585C=	NP_775265.1:p.Ser195=