Canonical Allele Identifier: CA348680051

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182707C>G (hg19) ; chr2:g.156326195C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326195C>G , CM000664.2:g.156326195C>G	GRCh38
NC_000002.11:g.157182707C>G , CM000664.1:g.157182707C>G	GRCh37
NC_000002.10:g.156890953C>G	NCBI36
NG_011821.1:g.11581G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1291G>C	ENSP00000514865.1:p.Asp431His
ENST00000700229.1:c.459G>C
ENST00000700230.1:c.1035G>C	ENSP00000514867.1:n.1035G>C
ENST00000700231.1:c.1420G>C	ENSP00000514868.1:p.Asp474His
ENST00000339562.9:c.1495G>C MANE Select	ENSP00000344479.4:p.Asp499His
ENST00000675870.1:c.*6G>C	ENSP00000502739.1:n.*6G>C
ENST00000339562.8:c.1495G>C	ENSP00000344479.4:p.Asp499His
ENST00000409108.6:c.1391G>C	ENSP00000386993.2:p.Arg464Pro
ENST00000409572.5:c.1495G>C	ENSP00000386747.1:p.Asp499His
ENST00000417764.5:c.*6G>C	ENSP00000415632.1:n.*6G>C
ENST00000417972.5:c.*6G>C	ENSP00000394671.1:n.*6G>C
ENST00000426264.5:c.1306G>C	ENSP00000389986.1:p.Asp436His
ENST00000429376.5:c.1202G>C	ENSP00000410952.1:p.Arg401Pro
NM_006186.3:c.1495G>C	NP_006177.1:p.Asp499His
XM_005246621.2:c.1528G>C	XP_005246678.1:p.Asp510His
XM_005246622.2:c.1306G>C	XP_005246679.1:p.Asp436His
XM_005246623.1:c.1306G>C	XP_005246680.1:p.Asp436His
XM_006712553.2:c.1453G>C	XP_006712616.1:p.Asp485His
XM_011511246.1:c.1424G>C	XP_011509548.1:p.Arg475Pro
XR_427087.2:n.3580G>C
NM_173173.2:c.1306G>C	NP_775265.1:p.Asp436His
XM_005246621.4:c.1528G>C	XP_005246678.1:p.Asp510His
XM_006712553.4:c.1453G>C	XP_006712616.1:p.Asp485His
XM_011511246.2:c.1424G>C	XP_011509548.1:p.Arg475Pro
XM_017004219.2:c.1495G>C	XP_016859708.1:p.Asp499His
XM_017004220.2:c.1420G>C	XP_016859709.1:p.Asp474His
XR_001738751.2:n.1742G>C
XR_001738752.2:n.1564G>C
XR_427087.4:n.1621G>C
NM_006186.4:c.1495G>C MANE Select	NP_006177.1:p.Asp499His
NM_173173.3:c.1306G>C	NP_775265.1:p.Asp436His