Canonical Allele Identifier: CA348681762

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157185947G>C (hg19) ; chr2:g.156329435G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329435G>C , CM000664.2:g.156329435G>C	GRCh38
NC_000002.11:g.157185947G>C , CM000664.1:g.157185947G>C	GRCh37
NC_000002.10:g.156894193G>C	NCBI36
NG_011821.1:g.8341C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.623C>G	ENSP00000514865.1:p.Pro208Arg
ENST00000700230.1:c.185C>G	ENSP00000514867.1:p.Pro62Arg
ENST00000700231.1:c.752C>G	ENSP00000514868.1:p.Pro251Arg
ENST00000339562.9:c.752C>G MANE Select	ENSP00000344479.4:p.Pro251Arg
ENST00000675870.1:c.563C>G	ENSP00000502739.1:p.Pro188Arg
ENST00000339562.8:c.752C>G	ENSP00000344479.4:p.Pro251Arg
ENST00000406048.2:c.208+479C>G
ENST00000409108.6:c.752C>G	ENSP00000386993.2:p.Pro251Arg
ENST00000409572.5:c.752C>G	ENSP00000386747.1:p.Pro251Arg
ENST00000417764.5:c.563C>G	ENSP00000415632.1:p.Pro188Arg
ENST00000417972.5:c.563C>G	ENSP00000394671.1:p.Pro188Arg
ENST00000424077.1:c.752C>G	ENSP00000406808.1:p.Pro251Arg
ENST00000426264.5:c.563C>G	ENSP00000389986.1:p.Pro188Arg
ENST00000429376.5:c.563C>G	ENSP00000410952.1:p.Pro188Arg
NM_006186.3:c.752C>G	NP_006177.1:p.Pro251Arg
XM_005246621.2:c.785C>G	XP_005246678.1:p.Pro262Arg
XM_005246622.2:c.563C>G	XP_005246679.1:p.Pro188Arg
XM_005246623.1:c.563C>G	XP_005246680.1:p.Pro188Arg
XM_006712553.2:c.785C>G	XP_006712616.1:p.Pro262Arg
XM_011511246.1:c.785C>G	XP_011509548.1:p.Pro262Arg
XR_427087.2:n.2958C>G
NM_173173.2:c.563C>G	NP_775265.1:p.Pro188Arg
XM_005246621.4:c.785C>G	XP_005246678.1:p.Pro262Arg
XM_006712553.4:c.785C>G	XP_006712616.1:p.Pro262Arg
XM_011511246.2:c.785C>G	XP_011509548.1:p.Pro262Arg
XM_017004219.2:c.752C>G	XP_016859708.1:p.Pro251Arg
XM_017004220.2:c.752C>G	XP_016859709.1:p.Pro251Arg
XR_001738751.2:n.1120C>G
XR_001738752.2:n.942C>G
XR_427087.4:n.999C>G
NM_006186.4:c.752C>G MANE Select	NP_006177.1:p.Pro251Arg
NM_173173.3:c.563C>G	NP_775265.1:p.Pro188Arg