Canonical Allele Identifier: CA759313212

Gene: NR4A2

Linked Data

• dbSNP Id: rs1367275844
• gnomAD v3: 2-156325659-A-ACGGCTAT
• gnomAD v4: 2-156325659-A-ACGGCTAT
• MyVariant Identifiers: chr2:g.157182171_157182172insCGGCTAT (hg19) ; chr2:g.156325659_156325660insCGGCTAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325661_156325667dup , CM000664.2:g.156325661_156325667dup	GRCh38
NC_000002.11:g.157182173_157182179dup , CM000664.1:g.157182173_157182179dup	GRCh37
NC_000002.10:g.156890419_156890425dup	NCBI36
NG_011821.1:g.12110_12116dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.*78_*84dup	ENSP00000514865.1:n.*78_*84dup
ENST00000700229.1:c.839_845dup
ENST00000700230.1:c.1415_1421dup	ENSP00000514867.1:n.1415_1421dup
ENST00000700231.1:c.*78_*84dup	ENSP00000514868.1:n.*78_*84dup
ENST00000339562.9:c.*78_*84dup MANE Select	ENSP00000344479.4:n.*78_*84dup
ENST00000675870.1:c.*386_*392dup	ENSP00000502739.1:n.*386_*392dup
ENST00000339562.8:c.*78_*84dup	ENSP00000344479.4:n.*78_*84dup
ENST00000409572.5:c.*78_*84dup	ENSP00000386747.1:n.*78_*84dup
ENST00000417764.5:c.*386_*392dup	ENSP00000415632.1:n.*386_*392dup
ENST00000417972.5:c.*386_*392dup	ENSP00000394671.1:n.*386_*392dup
ENST00000426264.5:c.*78_*84dup	ENSP00000389986.1:n.*78_*84dup
NM_006186.3:c.*78_*84dup	NP_006177.1:n.*78_*84dup
XM_005246621.2:c.*78_*84dup	XP_005246678.1:n.*78_*84dup
XM_005246622.2:c.*78_*84dup	XP_005246679.1:n.*78_*84dup
XM_005246623.1:c.*78_*84dup	XP_005246680.1:n.*78_*84dup
XM_006712553.2:c.*78_*84dup	XP_006712616.1:n.*78_*84dup
XM_011511246.1:c.*109_*115dup	XP_011509548.1:n.*109_*115dup
NM_173173.2:c.*78_*84dup	NP_775265.1:n.*78_*84dup
XM_005246621.4:c.*78_*84dup	XP_005246678.1:n.*78_*84dup
XM_006712553.4:c.*78_*84dup	XP_006712616.1:n.*78_*84dup
XM_011511246.2:c.*109_*115dup	XP_011509548.1:n.*109_*115dup
XM_017004219.2:c.*78_*84dup	XP_016859708.1:n.*78_*84dup
XM_017004220.2:c.*78_*84dup	XP_016859709.1:n.*78_*84dup
XR_001738751.2:n.2122_2128dup
XR_001738752.2:n.1944_1950dup
XR_427087.4:n.2001_2007dup
NM_006186.4:c.*78_*84dup MANE Select	NP_006177.1:n.*78_*84dup
NM_173173.3:c.*78_*84dup	NP_775265.1:n.*78_*84dup