Canonical Allele Identifier: CA348679363

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182313G>C (hg19) ; chr2:g.156325801G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325801G>C , CM000664.2:g.156325801G>C	GRCh38
NC_000002.11:g.157182313G>C , CM000664.1:g.157182313G>C	GRCh37
NC_000002.10:g.156890559G>C	NCBI36
NG_011821.1:g.11975C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1536C>G	ENSP00000514865.1:p.Asp512Glu
ENST00000700229.1:c.704C>G
ENST00000700230.1:c.1280C>G	ENSP00000514867.1:n.1280C>G
ENST00000700231.1:c.1665C>G	ENSP00000514868.1:p.Asp555Glu
ENST00000339562.9:c.1740C>G MANE Select	ENSP00000344479.4:p.Asp580Glu
ENST00000675870.1:c.*251C>G	ENSP00000502739.1:n.*251C>G
ENST00000339562.8:c.1740C>G	ENSP00000344479.4:p.Asp580Glu
ENST00000409108.6:c.1636C>G	ENSP00000386993.2:p.Leu546Val
ENST00000409572.5:c.1740C>G	ENSP00000386747.1:p.Asp580Glu
ENST00000417764.5:c.*251C>G	ENSP00000415632.1:n.*251C>G
ENST00000417972.5:c.*251C>G	ENSP00000394671.1:n.*251C>G
ENST00000426264.5:c.1551C>G	ENSP00000389986.1:p.Asp517Glu
ENST00000429376.5:c.1447C>G	ENSP00000410952.1:p.Leu483Val
NM_006186.3:c.1740C>G	NP_006177.1:p.Asp580Glu
XM_005246621.2:c.1773C>G	XP_005246678.1:p.Asp591Glu
XM_005246622.2:c.1551C>G	XP_005246679.1:p.Asp517Glu
XM_005246623.1:c.1551C>G	XP_005246680.1:p.Asp517Glu
XM_006712553.2:c.1698C>G	XP_006712616.1:p.Asp566Glu
XM_011511246.1:c.1669C>G	XP_011509548.1:p.Leu557Val
NM_173173.2:c.1551C>G	NP_775265.1:p.Asp517Glu
XM_005246621.4:c.1773C>G	XP_005246678.1:p.Asp591Glu
XM_006712553.4:c.1698C>G	XP_006712616.1:p.Asp566Glu
XM_011511246.2:c.1669C>G	XP_011509548.1:p.Leu557Val
XM_017004219.2:c.1740C>G	XP_016859708.1:p.Asp580Glu
XM_017004220.2:c.1665C>G	XP_016859709.1:p.Asp555Glu
XR_001738751.2:n.1987C>G
XR_001738752.2:n.1809C>G
XR_427087.4:n.1866C>G
NM_006186.4:c.1740C>G MANE Select	NP_006177.1:p.Asp580Glu
NM_173173.3:c.1551C>G	NP_775265.1:p.Asp517Glu