Canonical Allele Identifier: CA537223221

Gene: NR4A2

Linked Data

• dbSNP Id: rs1558864498
• gnomAD v2: 2-157182216-A-ATAACTGGAATGACAG
• gnomAD v4: 2-156325704-A-ATAACTGGAATGACAG
• MyVariant Identifiers: chr2:g.157182216_157182217insTAACTGGAATGACAG (hg19) ; chr2:g.156325704_156325705insTAACTGGAATGACAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325705_156325706insAACTGGAATGACAGT , CM000664.2:g.156325705_156325706insAACTGGAATGACAGT	GRCh38
NC_000002.11:g.157182217_157182218insAACTGGAATGACAGT , CM000664.1:g.157182217_157182218insAACTGGAATGACAGT	GRCh37
NC_000002.10:g.156890463_156890464insAACTGGAATGACAGT	NCBI36
NG_011821.1:g.12071_12072insCTGTCATTCCAGTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.*39_*40insCTGTCATTCCAGTTA	ENSP00000514865.1:n.*39_*40insCTGTCATTCCAGTTA
ENST00000700229.1:c.800_801insCTGTCATTCCAGTTA
ENST00000700230.1:c.1376_1377insCTGTCATTCCAGTTA	ENSP00000514867.1:n.1376_1377insCTGTCATTCCAGTTA
ENST00000700231.1:c.*39_*40insCTGTCATTCCAGTTA	ENSP00000514868.1:n.*39_*40insCTGTCATTCCAGTTA
ENST00000339562.9:c.*39_*40insCTGTCATTCCAGTTA MANE Select	ENSP00000344479.4:n.*39_*40insCTGTCATTCCAGTTA
ENST00000675870.1:c.*347_*348insCTGTCATTCCAGTTA	ENSP00000502739.1:n.*347_*348insCTGTCATTCCAGTTA
ENST00000339562.8:c.*39_*40insCTGTCATTCCAGTTA	ENSP00000344479.4:n.*39_*40insCTGTCATTCCAGTTA
ENST00000409572.5:c.*39_*40insCTGTCATTCCAGTTA	ENSP00000386747.1:n.*39_*40insCTGTCATTCCAGTTA
ENST00000417764.5:c.*347_*348insCTGTCATTCCAGTTA	ENSP00000415632.1:n.*347_*348insCTGTCATTCCAGTTA
ENST00000417972.5:c.*347_*348insCTGTCATTCCAGTTA	ENSP00000394671.1:n.*347_*348insCTGTCATTCCAGTTA
ENST00000426264.5:c.*39_*40insCTGTCATTCCAGTTA	ENSP00000389986.1:n.*39_*40insCTGTCATTCCAGTTA
NM_006186.3:c.*39_*40insCTGTCATTCCAGTTA	NP_006177.1:n.*39_*40insCTGTCATTCCAGTTA
XM_005246621.2:c.*39_*40insCTGTCATTCCAGTTA	XP_005246678.1:n.*39_*40insCTGTCATTCCAGTTA
XM_005246622.2:c.*39_*40insCTGTCATTCCAGTTA	XP_005246679.1:n.*39_*40insCTGTCATTCCAGTTA
XM_005246623.1:c.*39_*40insCTGTCATTCCAGTTA	XP_005246680.1:n.*39_*40insCTGTCATTCCAGTTA
XM_006712553.2:c.*39_*40insCTGTCATTCCAGTTA	XP_006712616.1:n.*39_*40insCTGTCATTCCAGTTA
XM_011511246.1:c.*70_*71insCTGTCATTCCAGTTA	XP_011509548.1:n.*70_*71insCTGTCATTCCAGTTA
NM_173173.2:c.*39_*40insCTGTCATTCCAGTTA	NP_775265.1:n.*39_*40insCTGTCATTCCAGTTA
XM_005246621.4:c.*39_*40insCTGTCATTCCAGTTA	XP_005246678.1:n.*39_*40insCTGTCATTCCAGTTA
XM_006712553.4:c.*39_*40insCTGTCATTCCAGTTA	XP_006712616.1:n.*39_*40insCTGTCATTCCAGTTA
XM_011511246.2:c.*70_*71insCTGTCATTCCAGTTA	XP_011509548.1:n.*70_*71insCTGTCATTCCAGTTA
XM_017004219.2:c.*39_*40insCTGTCATTCCAGTTA	XP_016859708.1:n.*39_*40insCTGTCATTCCAGTTA
XM_017004220.2:c.*39_*40insCTGTCATTCCAGTTA	XP_016859709.1:n.*39_*40insCTGTCATTCCAGTTA
XR_001738751.2:n.2083_2084insCTGTCATTCCAGTTA
XR_001738752.2:n.1905_1906insCTGTCATTCCAGTTA
XR_427087.4:n.1962_1963insCTGTCATTCCAGTTA
NM_006186.4:c.*39_*40insCTGTCATTCCAGTTA MANE Select	NP_006177.1:n.*39_*40insCTGTCATTCCAGTTA
NM_173173.3:c.*39_*40insCTGTCATTCCAGTTA	NP_775265.1:n.*39_*40insCTGTCATTCCAGTTA