Canonical Allele Identifier: CA429727637

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157186141C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329629C>G , CM000664.2:g.156329629C>G	GRCh38
NC_000002.11:g.157186141C>G , CM000664.1:g.157186141C>G	GRCh37
NC_000002.10:g.156894387C>G	NCBI36
NG_011821.1:g.8147G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.369G>C	ENSP00000388120.2:p.Pro123=
ENST00000700228.1:c.429G>C	ENSP00000514865.1:p.Pro143=
ENST00000700231.1:c.558G>C	ENSP00000514868.1:p.Pro186=
ENST00000339562.9:c.558G>C MANE Select	ENSP00000344479.4:p.Pro186=
ENST00000675870.1:c.369G>C	ENSP00000502739.1:p.Pro123=
ENST00000339562.8:c.558G>C	ENSP00000344479.4:p.Pro186=
ENST00000406048.2:c.208+285G>C
ENST00000409108.6:c.558G>C	ENSP00000386993.2:p.Pro186=
ENST00000409572.5:c.558G>C	ENSP00000386747.1:p.Pro186=
ENST00000417764.5:c.369G>C	ENSP00000415632.1:p.Pro123=
ENST00000417972.5:c.369G>C	ENSP00000394671.1:p.Pro123=
ENST00000424077.1:c.558G>C	ENSP00000406808.1:p.Pro186=
ENST00000426264.5:c.369G>C	ENSP00000389986.1:p.Pro123=
ENST00000429376.5:c.369G>C	ENSP00000410952.1:p.Pro123=
NM_006186.3:c.558G>C	NP_006177.1:p.Pro186=
XM_005246621.2:c.591G>C	XP_005246678.1:p.Pro197=
XM_005246622.2:c.369G>C	XP_005246679.1:p.Pro123=
XM_005246623.1:c.369G>C	XP_005246680.1:p.Pro123=
XM_006712553.2:c.591G>C	XP_006712616.1:p.Pro197=
XM_011511246.1:c.591G>C	XP_011509548.1:p.Pro197=
XR_427087.2:n.2764G>C
NM_173173.2:c.369G>C	NP_775265.1:p.Pro123=
XM_005246621.4:c.591G>C	XP_005246678.1:p.Pro197=
XM_006712553.4:c.591G>C	XP_006712616.1:p.Pro197=
XM_011511246.2:c.591G>C	XP_011509548.1:p.Pro197=
XM_017004219.2:c.558G>C	XP_016859708.1:p.Pro186=
XM_017004220.2:c.558G>C	XP_016859709.1:p.Pro186=
XR_001738751.2:n.926G>C
XR_001738752.2:n.748G>C
XR_427087.4:n.805G>C
NM_006186.4:c.558G>C MANE Select	NP_006177.1:p.Pro186=
NM_173173.3:c.369G>C	NP_775265.1:p.Pro123=