Canonical Allele Identifier: CA348679412

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182330A>C (hg19) ; chr2:g.156325818A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325818A>C , CM000664.2:g.156325818A>C	GRCh38
NC_000002.11:g.157182330A>C , CM000664.1:g.157182330A>C	GRCh37
NC_000002.10:g.156890576A>C	NCBI36
NG_011821.1:g.11958T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1519T>G	ENSP00000514865.1:p.Tyr507Asp
ENST00000700229.1:c.687T>G
ENST00000700230.1:c.1263T>G	ENSP00000514867.1:n.1263T>G
ENST00000700231.1:c.1648T>G	ENSP00000514868.1:p.Tyr550Asp
ENST00000339562.9:c.1723T>G MANE Select	ENSP00000344479.4:p.Tyr575Asp
ENST00000675870.1:c.*234T>G	ENSP00000502739.1:n.*234T>G
ENST00000339562.8:c.1723T>G	ENSP00000344479.4:p.Tyr575Asp
ENST00000409108.6:c.1619T>G	ENSP00000386993.2:p.Leu540Arg
ENST00000409572.5:c.1723T>G	ENSP00000386747.1:p.Tyr575Asp
ENST00000417764.5:c.*234T>G	ENSP00000415632.1:n.*234T>G
ENST00000417972.5:c.*234T>G	ENSP00000394671.1:n.*234T>G
ENST00000426264.5:c.1534T>G	ENSP00000389986.1:p.Tyr512Asp
ENST00000429376.5:c.1430T>G	ENSP00000410952.1:p.Leu477Arg
NM_006186.3:c.1723T>G	NP_006177.1:p.Tyr575Asp
XM_005246621.2:c.1756T>G	XP_005246678.1:p.Tyr586Asp
XM_005246622.2:c.1534T>G	XP_005246679.1:p.Tyr512Asp
XM_005246623.1:c.1534T>G	XP_005246680.1:p.Tyr512Asp
XM_006712553.2:c.1681T>G	XP_006712616.1:p.Tyr561Asp
XM_011511246.1:c.1652T>G	XP_011509548.1:p.Leu551Arg
NM_173173.2:c.1534T>G	NP_775265.1:p.Tyr512Asp
XM_005246621.4:c.1756T>G	XP_005246678.1:p.Tyr586Asp
XM_006712553.4:c.1681T>G	XP_006712616.1:p.Tyr561Asp
XM_011511246.2:c.1652T>G	XP_011509548.1:p.Leu551Arg
XM_017004219.2:c.1723T>G	XP_016859708.1:p.Tyr575Asp
XM_017004220.2:c.1648T>G	XP_016859709.1:p.Tyr550Asp
XR_001738751.2:n.1970T>G
XR_001738752.2:n.1792T>G
XR_427087.4:n.1849T>G
NM_006186.4:c.1723T>G MANE Select	NP_006177.1:p.Tyr575Asp
NM_173173.3:c.1534T>G	NP_775265.1:p.Tyr512Asp