Canonical Allele Identifier: CA348682660

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157186365C>G (hg19) ; chr2:g.156329853C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329853C>G , CM000664.2:g.156329853C>G	GRCh38
NC_000002.11:g.157186365C>G , CM000664.1:g.157186365C>G	GRCh37
NC_000002.10:g.156894611C>G	NCBI36
NG_011821.1:g.7923G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.145G>C	ENSP00000388120.2:p.Glu49Gln
ENST00000700228.1:c.205G>C	ENSP00000514865.1:p.Glu69Gln
ENST00000700231.1:c.334G>C	ENSP00000514868.1:p.Glu112Gln
ENST00000339562.9:c.334G>C MANE Select	ENSP00000344479.4:p.Glu112Gln
ENST00000675870.1:c.145G>C	ENSP00000502739.1:p.Glu49Gln
ENST00000339562.8:c.334G>C	ENSP00000344479.4:p.Glu112Gln
ENST00000406048.2:c.208+61G>C
ENST00000409108.6:c.334G>C	ENSP00000386993.2:p.Glu112Gln
ENST00000409572.5:c.334G>C	ENSP00000386747.1:p.Glu112Gln
ENST00000417764.5:c.145G>C	ENSP00000415632.1:p.Glu49Gln
ENST00000417972.5:c.145G>C	ENSP00000394671.1:p.Glu49Gln
ENST00000421709.1:c.145G>C	ENSP00000388120.1:p.Glu49Gln
ENST00000424077.1:c.334G>C	ENSP00000406808.1:p.Glu112Gln
ENST00000426264.5:c.145G>C	ENSP00000389986.1:p.Glu49Gln
ENST00000429376.5:c.145G>C	ENSP00000410952.1:p.Glu49Gln
NM_006186.3:c.334G>C	NP_006177.1:p.Glu112Gln
XM_005246621.2:c.367G>C	XP_005246678.1:p.Glu123Gln
XM_005246622.2:c.145G>C	XP_005246679.1:p.Glu49Gln
XM_005246623.1:c.145G>C	XP_005246680.1:p.Glu49Gln
XM_006712553.2:c.367G>C	XP_006712616.1:p.Glu123Gln
XM_011511246.1:c.367G>C	XP_011509548.1:p.Glu123Gln
XR_427087.2:n.2540G>C
NM_173173.2:c.145G>C	NP_775265.1:p.Glu49Gln
XM_005246621.4:c.367G>C	XP_005246678.1:p.Glu123Gln
XM_006712553.4:c.367G>C	XP_006712616.1:p.Glu123Gln
XM_011511246.2:c.367G>C	XP_011509548.1:p.Glu123Gln
XM_017004219.2:c.334G>C	XP_016859708.1:p.Glu112Gln
XM_017004220.2:c.334G>C	XP_016859709.1:p.Glu112Gln
XR_001738751.2:n.702G>C
XR_001738752.2:n.524G>C
XR_427087.4:n.581G>C
NM_006186.4:c.334G>C MANE Select	NP_006177.1:p.Glu112Gln
NM_173173.3:c.145G>C	NP_775265.1:p.Glu49Gln