Canonical Allele Identifier: CA348682067

Gene: NR4A2

Linked Data

• ClinVar Variation Id: 2261452
• ClinVar RCV Id: RCV002773204
• gnomAD v4: 2-156329582-A-G
• MyVariant Identifiers: chr2:g.157186094A>G (hg19) ; chr2:g.156329582A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329582A>G , CM000664.2:g.156329582A>G	GRCh38
NC_000002.11:g.157186094A>G , CM000664.1:g.157186094A>G	GRCh37
NC_000002.10:g.156894340A>G	NCBI36
NG_011821.1:g.8194T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.416T>C	ENSP00000388120.2:p.Met139Thr
ENST00000700228.1:c.476T>C	ENSP00000514865.1:p.Met159Thr
ENST00000700230.1:c.38T>C	ENSP00000514867.1:p.Met13Thr
ENST00000700231.1:c.605T>C	ENSP00000514868.1:p.Met202Thr
ENST00000339562.9:c.605T>C MANE Select	ENSP00000344479.4:p.Met202Thr
ENST00000675870.1:c.416T>C	ENSP00000502739.1:p.Met139Thr
ENST00000339562.8:c.605T>C	ENSP00000344479.4:p.Met202Thr
ENST00000406048.2:c.208+332T>C
ENST00000409108.6:c.605T>C	ENSP00000386993.2:p.Met202Thr
ENST00000409572.5:c.605T>C	ENSP00000386747.1:p.Met202Thr
ENST00000417764.5:c.416T>C	ENSP00000415632.1:p.Met139Thr
ENST00000417972.5:c.416T>C	ENSP00000394671.1:p.Met139Thr
ENST00000424077.1:c.605T>C	ENSP00000406808.1:p.Met202Thr
ENST00000426264.5:c.416T>C	ENSP00000389986.1:p.Met139Thr
ENST00000429376.5:c.416T>C	ENSP00000410952.1:p.Met139Thr
NM_006186.3:c.605T>C	NP_006177.1:p.Met202Thr
XM_005246621.2:c.638T>C	XP_005246678.1:p.Met213Thr
XM_005246622.2:c.416T>C	XP_005246679.1:p.Met139Thr
XM_005246623.1:c.416T>C	XP_005246680.1:p.Met139Thr
XM_006712553.2:c.638T>C	XP_006712616.1:p.Met213Thr
XM_011511246.1:c.638T>C	XP_011509548.1:p.Met213Thr
XR_427087.2:n.2811T>C
NM_173173.2:c.416T>C	NP_775265.1:p.Met139Thr
XM_005246621.4:c.638T>C	XP_005246678.1:p.Met213Thr
XM_006712553.4:c.638T>C	XP_006712616.1:p.Met213Thr
XM_011511246.2:c.638T>C	XP_011509548.1:p.Met213Thr
XM_017004219.2:c.605T>C	XP_016859708.1:p.Met202Thr
XM_017004220.2:c.605T>C	XP_016859709.1:p.Met202Thr
XR_001738751.2:n.973T>C
XR_001738752.2:n.795T>C
XR_427087.4:n.852T>C
NM_006186.4:c.605T>C MANE Select	NP_006177.1:p.Met202Thr
NM_173173.3:c.416T>C	NP_775265.1:p.Met139Thr