Canonical Allele Identifier: CA348679807

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325962G>C , CM000664.2:g.156325962G>C	GRCh38
NC_000002.11:g.157182474G>C , CM000664.1:g.157182474G>C	GRCh37
NC_000002.10:g.156890720G>C	NCBI36
NG_011821.1:g.11814C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006186.4:c.1579C>G MANE Select	NP_006177.1:p.Leu527Val
ENST00000339562.9:c.1579C>G MANE Select	ENSP00000344479.4:p.Leu527Val
NM_006186.3:c.1579C>G	NP_006177.1:p.Leu527Val
NM_173173.2:c.1390C>G	NP_775265.1:p.Leu464Val
NM_173173.3:c.1390C>G	NP_775265.1:p.Leu464Val
ENST00000339562.8:c.1579C>G	ENSP00000344479.4:p.Leu527Val
ENST00000409108.6:c.1475C>G	ENSP00000386993.2:p.Thr492Ser
ENST00000409572.5:c.1579C>G	ENSP00000386747.1:p.Leu527Val
ENST00000417764.5:c.*90C>G	ENSP00000415632.1:n.*90C>G
ENST00000417972.5:c.*90C>G	ENSP00000394671.1:n.*90C>G
ENST00000426264.5:c.1390C>G	ENSP00000389986.1:p.Leu464Val
ENST00000429376.5:c.1286C>G	ENSP00000410952.1:p.Thr429Ser
ENST00000675870.1:c.*90C>G	ENSP00000502739.1:n.*90C>G
ENST00000700228.1:c.1375C>G	ENSP00000514865.1:p.Leu459Val
ENST00000700229.1:c.543C>G
ENST00000700230.1:c.1119C>G	ENSP00000514867.1:n.1119C>G
ENST00000700231.1:c.1504C>G	ENSP00000514868.1:p.Leu502Val
XM_005246621.2:c.1612C>G	XP_005246678.1:p.Leu538Val
XM_005246621.4:c.1612C>G	XP_005246678.1:p.Leu538Val
XM_005246622.2:c.1390C>G	XP_005246679.1:p.Leu464Val
XM_005246623.1:c.1390C>G	XP_005246680.1:p.Leu464Val
XM_006712553.2:c.1537C>G	XP_006712616.1:p.Leu513Val
XM_006712553.4:c.1537C>G	XP_006712616.1:p.Leu513Val
XM_011511246.1:c.1508C>G	XP_011509548.1:p.Thr503Ser
XM_011511246.2:c.1508C>G	XP_011509548.1:p.Thr503Ser
XM_017004219.2:c.1579C>G	XP_016859708.1:p.Leu527Val
XM_017004220.2:c.1504C>G	XP_016859709.1:p.Leu502Val
XR_001738751.2:n.1826C>G
XR_001738752.2:n.1648C>G
XR_427087.4:n.1705C>G