Canonical Allele Identifier: CA348679887

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182503C>G (hg19) ; chr2:g.156325991C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325991C>G , CM000664.2:g.156325991C>G	GRCh38
NC_000002.11:g.157182503C>G , CM000664.1:g.157182503C>G	GRCh37
NC_000002.10:g.156890749C>G	NCBI36
NG_011821.1:g.11785G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1346G>C	ENSP00000514865.1:p.Gly449Ala
ENST00000700229.1:c.514G>C
ENST00000700230.1:c.1090G>C	ENSP00000514867.1:n.1090G>C
ENST00000700231.1:c.1475G>C	ENSP00000514868.1:p.Gly492Ala
ENST00000339562.9:c.1550G>C MANE Select	ENSP00000344479.4:p.Gly517Ala
ENST00000675870.1:c.*61G>C	ENSP00000502739.1:n.*61G>C
ENST00000339562.8:c.1550G>C	ENSP00000344479.4:p.Gly517Ala
ENST00000409108.6:c.1446G>C	ENSP00000386993.2:p.Arg482=
ENST00000409572.5:c.1550G>C	ENSP00000386747.1:p.Gly517Ala
ENST00000417764.5:c.*61G>C	ENSP00000415632.1:n.*61G>C
ENST00000417972.5:c.*61G>C	ENSP00000394671.1:n.*61G>C
ENST00000426264.5:c.1361G>C	ENSP00000389986.1:p.Gly454Ala
ENST00000429376.5:c.1257G>C	ENSP00000410952.1:p.Arg419=
NM_006186.3:c.1550G>C	NP_006177.1:p.Gly517Ala
XM_005246621.2:c.1583G>C	XP_005246678.1:p.Gly528Ala
XM_005246622.2:c.1361G>C	XP_005246679.1:p.Gly454Ala
XM_005246623.1:c.1361G>C	XP_005246680.1:p.Gly454Ala
XM_006712553.2:c.1508G>C	XP_006712616.1:p.Gly503Ala
XM_011511246.1:c.1479G>C	XP_011509548.1:p.Arg493=
XR_427087.2:n.3635G>C
NM_173173.2:c.1361G>C	NP_775265.1:p.Gly454Ala
XM_005246621.4:c.1583G>C	XP_005246678.1:p.Gly528Ala
XM_006712553.4:c.1508G>C	XP_006712616.1:p.Gly503Ala
XM_011511246.2:c.1479G>C	XP_011509548.1:p.Arg493=
XM_017004219.2:c.1550G>C	XP_016859708.1:p.Gly517Ala
XM_017004220.2:c.1475G>C	XP_016859709.1:p.Gly492Ala
XR_001738751.2:n.1797G>C
XR_001738752.2:n.1619G>C
XR_427087.4:n.1676G>C
NM_006186.4:c.1550G>C MANE Select	NP_006177.1:p.Gly517Ala
NM_173173.3:c.1361G>C	NP_775265.1:p.Gly454Ala