Canonical Allele Identifier: CA348681757

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157185944G>C (hg19) ; chr2:g.156329432G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329432G>C , CM000664.2:g.156329432G>C	GRCh38
NC_000002.11:g.157185944G>C , CM000664.1:g.157185944G>C	GRCh37
NC_000002.10:g.156894190G>C	NCBI36
NG_011821.1:g.8344C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.626C>G	ENSP00000514865.1:p.Pro209Arg
ENST00000700230.1:c.188C>G	ENSP00000514867.1:p.Pro63Arg
ENST00000700231.1:c.755C>G	ENSP00000514868.1:p.Pro252Arg
ENST00000339562.9:c.755C>G MANE Select	ENSP00000344479.4:p.Pro252Arg
ENST00000675870.1:c.566C>G	ENSP00000502739.1:p.Pro189Arg
ENST00000339562.8:c.755C>G	ENSP00000344479.4:p.Pro252Arg
ENST00000406048.2:c.208+482C>G
ENST00000409108.6:c.755C>G	ENSP00000386993.2:p.Pro252Arg
ENST00000409572.5:c.755C>G	ENSP00000386747.1:p.Pro252Arg
ENST00000417764.5:c.566C>G	ENSP00000415632.1:p.Pro189Arg
ENST00000417972.5:c.566C>G	ENSP00000394671.1:p.Pro189Arg
ENST00000424077.1:c.755C>G	ENSP00000406808.1:p.Pro252Arg
ENST00000426264.5:c.566C>G	ENSP00000389986.1:p.Pro189Arg
ENST00000429376.5:c.566C>G	ENSP00000410952.1:p.Pro189Arg
NM_006186.3:c.755C>G	NP_006177.1:p.Pro252Arg
XM_005246621.2:c.788C>G	XP_005246678.1:p.Pro263Arg
XM_005246622.2:c.566C>G	XP_005246679.1:p.Pro189Arg
XM_005246623.1:c.566C>G	XP_005246680.1:p.Pro189Arg
XM_006712553.2:c.788C>G	XP_006712616.1:p.Pro263Arg
XM_011511246.1:c.788C>G	XP_011509548.1:p.Pro263Arg
XR_427087.2:n.2961C>G
NM_173173.2:c.566C>G	NP_775265.1:p.Pro189Arg
XM_005246621.4:c.788C>G	XP_005246678.1:p.Pro263Arg
XM_006712553.4:c.788C>G	XP_006712616.1:p.Pro263Arg
XM_011511246.2:c.788C>G	XP_011509548.1:p.Pro263Arg
XM_017004219.2:c.755C>G	XP_016859708.1:p.Pro252Arg
XM_017004220.2:c.755C>G	XP_016859709.1:p.Pro252Arg
XR_001738751.2:n.1123C>G
XR_001738752.2:n.945C>G
XR_427087.4:n.1002C>G
NM_006186.4:c.755C>G MANE Select	NP_006177.1:p.Pro252Arg
NM_173173.3:c.566C>G	NP_775265.1:p.Pro189Arg