Canonical Allele Identifier: CA348680066

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182714C>G (hg19) ; chr2:g.156326202C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326202C>G , CM000664.2:g.156326202C>G	GRCh38
NC_000002.11:g.157182714C>G , CM000664.1:g.157182714C>G	GRCh37
NC_000002.10:g.156890960C>G	NCBI36
NG_011821.1:g.11574G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1284G>C	ENSP00000514865.1:p.Met428Ile
ENST00000700229.1:c.452G>C
ENST00000700230.1:c.1028G>C	ENSP00000514867.1:n.1028G>C
ENST00000700231.1:c.1413G>C	ENSP00000514868.1:p.Met471Ile
ENST00000339562.9:c.1488G>C MANE Select	ENSP00000344479.4:p.Met496Ile
ENST00000675870.1:c.1178G>C	ENSP00000502739.1:p.Ter393Ser
ENST00000339562.8:c.1488G>C	ENSP00000344479.4:p.Met496Ile
ENST00000409108.6:c.1384G>C	ENSP00000386993.2:p.Glu462Gln
ENST00000409572.5:c.1488G>C	ENSP00000386747.1:p.Met496Ile
ENST00000417764.5:c.1178G>C	ENSP00000415632.1:p.Ter393Ser
ENST00000417972.5:c.1178G>C	ENSP00000394671.1:p.Ter393Ser
ENST00000426264.5:c.1299G>C	ENSP00000389986.1:p.Met433Ile
ENST00000429376.5:c.1195G>C	ENSP00000410952.1:p.Glu399Gln
NM_006186.3:c.1488G>C	NP_006177.1:p.Met496Ile
XM_005246621.2:c.1521G>C	XP_005246678.1:p.Met507Ile
XM_005246622.2:c.1299G>C	XP_005246679.1:p.Met433Ile
XM_005246623.1:c.1299G>C	XP_005246680.1:p.Met433Ile
XM_006712553.2:c.1446G>C	XP_006712616.1:p.Met482Ile
XM_011511246.1:c.1417G>C	XP_011509548.1:p.Glu473Gln
XR_427087.2:n.3573G>C
NM_173173.2:c.1299G>C	NP_775265.1:p.Met433Ile
XM_005246621.4:c.1521G>C	XP_005246678.1:p.Met507Ile
XM_006712553.4:c.1446G>C	XP_006712616.1:p.Met482Ile
XM_011511246.2:c.1417G>C	XP_011509548.1:p.Glu473Gln
XM_017004219.2:c.1488G>C	XP_016859708.1:p.Met496Ile
XM_017004220.2:c.1413G>C	XP_016859709.1:p.Met471Ile
XR_001738751.2:n.1735G>C
XR_001738752.2:n.1557G>C
XR_427087.4:n.1614G>C
NM_006186.4:c.1488G>C MANE Select	NP_006177.1:p.Met496Ile
NM_173173.3:c.1299G>C	NP_775265.1:p.Met433Ile