Canonical Allele Identifier: CA348680021

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182696G>C (hg19) ; chr2:g.156326184G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326184G>C , CM000664.2:g.156326184G>C	GRCh38
NC_000002.11:g.157182696G>C , CM000664.1:g.157182696G>C	GRCh37
NC_000002.10:g.156890942G>C	NCBI36
NG_011821.1:g.11592C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1302C>G	ENSP00000514865.1:p.Ala434=
ENST00000700229.1:c.470C>G
ENST00000700230.1:c.1046C>G	ENSP00000514867.1:n.1046C>G
ENST00000700231.1:c.1431C>G	ENSP00000514868.1:p.Ala477=
ENST00000339562.9:c.1506C>G MANE Select	ENSP00000344479.4:p.Ala502=
ENST00000675870.1:c.*17C>G	ENSP00000502739.1:n.*17C>G
ENST00000339562.8:c.1506C>G	ENSP00000344479.4:p.Ala502=
ENST00000409108.6:c.1402C>G	ENSP00000386993.2:p.Leu468Val
ENST00000409572.5:c.1506C>G	ENSP00000386747.1:p.Ala502=
ENST00000417764.5:c.*17C>G	ENSP00000415632.1:n.*17C>G
ENST00000417972.5:c.*17C>G	ENSP00000394671.1:n.*17C>G
ENST00000426264.5:c.1317C>G	ENSP00000389986.1:p.Ala439=
ENST00000429376.5:c.1213C>G	ENSP00000410952.1:p.Leu405Val
NM_006186.3:c.1506C>G	NP_006177.1:p.Ala502=
XM_005246621.2:c.1539C>G	XP_005246678.1:p.Ala513=
XM_005246622.2:c.1317C>G	XP_005246679.1:p.Ala439=
XM_005246623.1:c.1317C>G	XP_005246680.1:p.Ala439=
XM_006712553.2:c.1464C>G	XP_006712616.1:p.Ala488=
XM_011511246.1:c.1435C>G	XP_011509548.1:p.Leu479Val
XR_427087.2:n.3591C>G
NM_173173.2:c.1317C>G	NP_775265.1:p.Ala439=
XM_005246621.4:c.1539C>G	XP_005246678.1:p.Ala513=
XM_006712553.4:c.1464C>G	XP_006712616.1:p.Ala488=
XM_011511246.2:c.1435C>G	XP_011509548.1:p.Leu479Val
XM_017004219.2:c.1506C>G	XP_016859708.1:p.Ala502=
XM_017004220.2:c.1431C>G	XP_016859709.1:p.Ala477=
XR_001738751.2:n.1753C>G
XR_001738752.2:n.1575C>G
XR_427087.4:n.1632C>G
NM_006186.4:c.1506C>G MANE Select	NP_006177.1:p.Ala502=
NM_173173.3:c.1317C>G	NP_775265.1:p.Ala439=