Canonical Allele Identifier: CA348680044

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182704T>C (hg19) ; chr2:g.156326192T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326192T>C , CM000664.2:g.156326192T>C	GRCh38
NC_000002.11:g.157182704T>C , CM000664.1:g.157182704T>C	GRCh37
NC_000002.10:g.156890950T>C	NCBI36
NG_011821.1:g.11584A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1294A>G	ENSP00000514865.1:p.Ile432Val
ENST00000700229.1:c.462A>G
ENST00000700230.1:c.1038A>G	ENSP00000514867.1:n.1038A>G
ENST00000700231.1:c.1423A>G	ENSP00000514868.1:p.Ile475Val
ENST00000339562.9:c.1498A>G MANE Select	ENSP00000344479.4:p.Ile500Val
ENST00000675870.1:c.*9A>G	ENSP00000502739.1:n.*9A>G
ENST00000339562.8:c.1498A>G	ENSP00000344479.4:p.Ile500Val
ENST00000409108.6:c.1394A>G	ENSP00000386993.2:p.His465Arg
ENST00000409572.5:c.1498A>G	ENSP00000386747.1:p.Ile500Val
ENST00000417764.5:c.*9A>G	ENSP00000415632.1:n.*9A>G
ENST00000417972.5:c.*9A>G	ENSP00000394671.1:n.*9A>G
ENST00000426264.5:c.1309A>G	ENSP00000389986.1:p.Ile437Val
ENST00000429376.5:c.1205A>G	ENSP00000410952.1:p.His402Arg
NM_006186.3:c.1498A>G	NP_006177.1:p.Ile500Val
XM_005246621.2:c.1531A>G	XP_005246678.1:p.Ile511Val
XM_005246622.2:c.1309A>G	XP_005246679.1:p.Ile437Val
XM_005246623.1:c.1309A>G	XP_005246680.1:p.Ile437Val
XM_006712553.2:c.1456A>G	XP_006712616.1:p.Ile486Val
XM_011511246.1:c.1427A>G	XP_011509548.1:p.His476Arg
XR_427087.2:n.3583A>G
NM_173173.2:c.1309A>G	NP_775265.1:p.Ile437Val
XM_005246621.4:c.1531A>G	XP_005246678.1:p.Ile511Val
XM_006712553.4:c.1456A>G	XP_006712616.1:p.Ile486Val
XM_011511246.2:c.1427A>G	XP_011509548.1:p.His476Arg
XM_017004219.2:c.1498A>G	XP_016859708.1:p.Ile500Val
XM_017004220.2:c.1423A>G	XP_016859709.1:p.Ile475Val
XR_001738751.2:n.1745A>G
XR_001738752.2:n.1567A>G
XR_427087.4:n.1624A>G
NM_006186.4:c.1498A>G MANE Select	NP_006177.1:p.Ile500Val
NM_173173.3:c.1309A>G	NP_775265.1:p.Ile437Val