Canonical Allele Identifier: CA1300460508

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329578G= , CM000664.2:g.156329578G=	GRCh38
NC_000002.11:g.157186090G= , CM000664.1:g.157186090G=	GRCh37
NC_000002.10:g.156894336G=	NCBI36
NG_011821.1:g.8198C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.420C=	ENSP00000388120.2:p.Asn140=
ENST00000700228.1:c.480C=	ENSP00000514865.1:p.Asn160=
ENST00000700230.1:c.42C=	ENSP00000514867.1:p.Asn14=
ENST00000700231.1:c.609C=	ENSP00000514868.1:p.Asn203=
ENST00000339562.9:c.609C= MANE Select	ENSP00000344479.4:p.Asn203=
ENST00000675870.1:c.420C=	ENSP00000502739.1:p.Asn140=
ENST00000339562.8:c.609C=	ENSP00000344479.4:p.Asn203=
ENST00000406048.2:c.208+336C=
ENST00000409108.6:c.609C=	ENSP00000386993.2:p.Asn203=
ENST00000409572.5:c.609C=	ENSP00000386747.1:p.Asn203=
ENST00000417764.5:c.420C=	ENSP00000415632.1:p.Asn140=
ENST00000417972.5:c.420C=	ENSP00000394671.1:p.Asn140=
ENST00000424077.1:c.609C=	ENSP00000406808.1:p.Asn203=
ENST00000426264.5:c.420C=	ENSP00000389986.1:p.Asn140=
ENST00000429376.5:c.420C=	ENSP00000410952.1:p.Asn140=
NM_006186.3:c.609C=	NP_006177.1:p.Asn203=
XM_005246621.2:c.642C=	XP_005246678.1:p.Asn214=
XM_005246622.2:c.420C=	XP_005246679.1:p.Asn140=
XM_005246623.1:c.420C=	XP_005246680.1:p.Asn140=
XM_006712553.2:c.642C=	XP_006712616.1:p.Asn214=
XM_011511246.1:c.642C=	XP_011509548.1:p.Asn214=
XR_427087.2:n.2815C=
NM_173173.2:c.420C=	NP_775265.1:p.Asn140=
XM_005246621.4:c.642C=	XP_005246678.1:p.Asn214=
XM_006712553.4:c.642C=	XP_006712616.1:p.Asn214=
XM_011511246.2:c.642C=	XP_011509548.1:p.Asn214=
XM_017004219.2:c.609C=	XP_016859708.1:p.Asn203=
XM_017004220.2:c.609C=	XP_016859709.1:p.Asn203=
XR_001738751.2:n.977C=
XR_001738752.2:n.799C=
XR_427087.4:n.856C=
NM_006186.4:c.609C= MANE Select	NP_006177.1:p.Asn203=
NM_173173.3:c.420C=	NP_775265.1:p.Asn140=