Canonical Allele Identifier: CA348680075

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182717A>G (hg19) ; chr2:g.156326205A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326205A>G , CM000664.2:g.156326205A>G	GRCh38
NC_000002.11:g.157182717A>G , CM000664.1:g.157182717A>G	GRCh37
NC_000002.10:g.156890963A>G	NCBI36
NG_011821.1:g.11571T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1281T>C	ENSP00000514865.1:p.Asn427=
ENST00000700229.1:c.449T>C
ENST00000700230.1:c.1025T>C	ENSP00000514867.1:n.1025T>C
ENST00000700231.1:c.1410T>C	ENSP00000514868.1:p.Asn470=
ENST00000339562.9:c.1485T>C MANE Select	ENSP00000344479.4:p.Asn495=
ENST00000675870.1:c.1175T>C	ENSP00000502739.1:p.Ile392Thr
ENST00000339562.8:c.1485T>C	ENSP00000344479.4:p.Asn495=
ENST00000409108.6:c.1381T>C	ENSP00000386993.2:p.Tyr461His
ENST00000409572.5:c.1485T>C	ENSP00000386747.1:p.Asn495=
ENST00000417764.5:c.1175T>C	ENSP00000415632.1:p.Ile392Thr
ENST00000417972.5:c.1175T>C	ENSP00000394671.1:p.Ile392Thr
ENST00000426264.5:c.1296T>C	ENSP00000389986.1:p.Asn432=
ENST00000429376.5:c.1192T>C	ENSP00000410952.1:p.Tyr398His
NM_006186.3:c.1485T>C	NP_006177.1:p.Asn495=
XM_005246621.2:c.1518T>C	XP_005246678.1:p.Asn506=
XM_005246622.2:c.1296T>C	XP_005246679.1:p.Asn432=
XM_005246623.1:c.1296T>C	XP_005246680.1:p.Asn432=
XM_006712553.2:c.1443T>C	XP_006712616.1:p.Asn481=
XM_011511246.1:c.1414T>C	XP_011509548.1:p.Tyr472His
XR_427087.2:n.3570T>C
NM_173173.2:c.1296T>C	NP_775265.1:p.Asn432=
XM_005246621.4:c.1518T>C	XP_005246678.1:p.Asn506=
XM_006712553.4:c.1443T>C	XP_006712616.1:p.Asn481=
XM_011511246.2:c.1414T>C	XP_011509548.1:p.Tyr472His
XM_017004219.2:c.1485T>C	XP_016859708.1:p.Asn495=
XM_017004220.2:c.1410T>C	XP_016859709.1:p.Asn470=
XR_001738751.2:n.1732T>C
XR_001738752.2:n.1554T>C
XR_427087.4:n.1611T>C
NM_006186.4:c.1485T>C MANE Select	NP_006177.1:p.Asn495=
NM_173173.3:c.1296T>C	NP_775265.1:p.Asn432=