Canonical Allele Identifier: CA348682709

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157186388C>G (hg19) ; chr2:g.156329876C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329876C>G , CM000664.2:g.156329876C>G	GRCh38
NC_000002.11:g.157186388C>G , CM000664.1:g.157186388C>G	GRCh37
NC_000002.10:g.156894634C>G	NCBI36
NG_011821.1:g.7900G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.122G>C	ENSP00000388120.2:p.Ser41Thr
ENST00000700228.1:c.182G>C	ENSP00000514865.1:p.Ser61Thr
ENST00000700231.1:c.311G>C	ENSP00000514868.1:p.Ser104Thr
ENST00000339562.9:c.311G>C MANE Select	ENSP00000344479.4:p.Ser104Thr
ENST00000675870.1:c.122G>C	ENSP00000502739.1:p.Ser41Thr
ENST00000339562.8:c.311G>C	ENSP00000344479.4:p.Ser104Thr
ENST00000406048.2:c.208+38G>C
ENST00000409108.6:c.311G>C	ENSP00000386993.2:p.Ser104Thr
ENST00000409572.5:c.311G>C	ENSP00000386747.1:p.Ser104Thr
ENST00000417764.5:c.122G>C	ENSP00000415632.1:p.Ser41Thr
ENST00000417972.5:c.122G>C	ENSP00000394671.1:p.Ser41Thr
ENST00000421709.1:c.122G>C	ENSP00000388120.1:p.Ser41Thr
ENST00000424077.1:c.311G>C	ENSP00000406808.1:p.Ser104Thr
ENST00000426264.5:c.122G>C	ENSP00000389986.1:p.Ser41Thr
ENST00000429376.5:c.122G>C	ENSP00000410952.1:p.Ser41Thr
NM_006186.3:c.311G>C	NP_006177.1:p.Ser104Thr
XM_005246621.2:c.344G>C	XP_005246678.1:p.Ser115Thr
XM_005246622.2:c.122G>C	XP_005246679.1:p.Ser41Thr
XM_005246623.1:c.122G>C	XP_005246680.1:p.Ser41Thr
XM_006712553.2:c.344G>C	XP_006712616.1:p.Ser115Thr
XM_011511246.1:c.344G>C	XP_011509548.1:p.Ser115Thr
XR_427087.2:n.2517G>C
NM_173173.2:c.122G>C	NP_775265.1:p.Ser41Thr
XM_005246621.4:c.344G>C	XP_005246678.1:p.Ser115Thr
XM_006712553.4:c.344G>C	XP_006712616.1:p.Ser115Thr
XM_011511246.2:c.344G>C	XP_011509548.1:p.Ser115Thr
XM_017004219.2:c.311G>C	XP_016859708.1:p.Ser104Thr
XM_017004220.2:c.311G>C	XP_016859709.1:p.Ser104Thr
XR_001738751.2:n.679G>C
XR_001738752.2:n.501G>C
XR_427087.4:n.558G>C
NM_006186.4:c.311G>C MANE Select	NP_006177.1:p.Ser104Thr
NM_173173.3:c.122G>C	NP_775265.1:p.Ser41Thr