Canonical Allele Identifier: CA429727707

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157185937C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329425C>T , CM000664.2:g.156329425C>T	GRCh38
NC_000002.11:g.157185937C>T , CM000664.1:g.157185937C>T	GRCh37
NC_000002.10:g.156894183C>T	NCBI36
NG_011821.1:g.8351G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.633G>A	ENSP00000514865.1:p.Arg211=
ENST00000700230.1:c.195G>A	ENSP00000514867.1:p.Arg65=
ENST00000700231.1:c.762G>A	ENSP00000514868.1:p.Arg254=
ENST00000339562.9:c.762G>A MANE Select	ENSP00000344479.4:p.Arg254=
ENST00000675870.1:c.573G>A	ENSP00000502739.1:p.Arg191=
ENST00000339562.8:c.762G>A	ENSP00000344479.4:p.Arg254=
ENST00000406048.2:c.208+489G>A
ENST00000409108.6:c.762G>A	ENSP00000386993.2:p.Arg254=
ENST00000409572.5:c.762G>A	ENSP00000386747.1:p.Arg254=
ENST00000417764.5:c.573G>A	ENSP00000415632.1:p.Arg191=
ENST00000417972.5:c.573G>A	ENSP00000394671.1:p.Arg191=
ENST00000424077.1:c.762G>A	ENSP00000406808.1:p.Arg254=
ENST00000426264.5:c.573G>A	ENSP00000389986.1:p.Arg191=
ENST00000429376.5:c.573G>A	ENSP00000410952.1:p.Arg191=
NM_006186.3:c.762G>A	NP_006177.1:p.Arg254=
XM_005246621.2:c.795G>A	XP_005246678.1:p.Arg265=
XM_005246622.2:c.573G>A	XP_005246679.1:p.Arg191=
XM_005246623.1:c.573G>A	XP_005246680.1:p.Arg191=
XM_006712553.2:c.795G>A	XP_006712616.1:p.Arg265=
XM_011511246.1:c.795G>A	XP_011509548.1:p.Arg265=
XR_427087.2:n.2968G>A
NM_173173.2:c.573G>A	NP_775265.1:p.Arg191=
XM_005246621.4:c.795G>A	XP_005246678.1:p.Arg265=
XM_006712553.4:c.795G>A	XP_006712616.1:p.Arg265=
XM_011511246.2:c.795G>A	XP_011509548.1:p.Arg265=
XM_017004219.2:c.762G>A	XP_016859708.1:p.Arg254=
XM_017004220.2:c.762G>A	XP_016859709.1:p.Arg254=
XR_001738751.2:n.1130G>A
XR_001738752.2:n.952G>A
XR_427087.4:n.1009G>A
NM_006186.4:c.762G>A MANE Select	NP_006177.1:p.Arg254=
NM_173173.3:c.573G>A	NP_775265.1:p.Arg191=