Canonical Allele Identifier: CA1038197724

Gene: NR4A2

Linked Data

• dbSNP Id: rs1686613432
• gnomAD v3: 2-156325729-G-GCC
• gnomAD v4: 2-156325729-G-GCC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325730_156325731insCC , CM000664.2:g.156325730_156325731insCC	GRCh38
NC_000002.11:g.157182242_157182243insCC , CM000664.1:g.157182242_157182243insCC	GRCh37
NC_000002.10:g.156890488_156890489insCC	NCBI36
NG_011821.1:g.12046_12047insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.*14_*15insGG	ENSP00000514865.1:n.*14_*15insGG
ENST00000700229.1:c.775_776insGG
ENST00000700230.1:c.1351_1352insGG	ENSP00000514867.1:n.1351_1352insGG
ENST00000700231.1:c.*14_*15insGG	ENSP00000514868.1:n.*14_*15insGG
ENST00000339562.9:c.*14_*15insGG MANE Select	ENSP00000344479.4:n.*14_*15insGG
ENST00000675870.1:c.*322_*323insGG	ENSP00000502739.1:n.*322_*323insGG
ENST00000339562.8:c.*14_*15insGG	ENSP00000344479.4:n.*14_*15insGG
ENST00000409572.5:c.*14_*15insGG	ENSP00000386747.1:n.*14_*15insGG
ENST00000417764.5:c.*322_*323insGG	ENSP00000415632.1:n.*322_*323insGG
ENST00000417972.5:c.*322_*323insGG	ENSP00000394671.1:n.*322_*323insGG
ENST00000426264.5:c.*14_*15insGG	ENSP00000389986.1:n.*14_*15insGG
NM_006186.3:c.*14_*15insGG	NP_006177.1:n.*14_*15insGG
XM_005246621.2:c.*14_*15insGG	XP_005246678.1:n.*14_*15insGG
XM_005246622.2:c.*14_*15insGG	XP_005246679.1:n.*14_*15insGG
XM_005246623.1:c.*14_*15insGG	XP_005246680.1:n.*14_*15insGG
XM_006712553.2:c.*14_*15insGG	XP_006712616.1:n.*14_*15insGG
XM_011511246.1:c.*45_*46insGG	XP_011509548.1:n.*45_*46insGG
NM_173173.2:c.*14_*15insGG	NP_775265.1:n.*14_*15insGG
XM_005246621.4:c.*14_*15insGG	XP_005246678.1:n.*14_*15insGG
XM_006712553.4:c.*14_*15insGG	XP_006712616.1:n.*14_*15insGG
XM_011511246.2:c.*45_*46insGG	XP_011509548.1:n.*45_*46insGG
XM_017004219.2:c.*14_*15insGG	XP_016859708.1:n.*14_*15insGG
XM_017004220.2:c.*14_*15insGG	XP_016859709.1:n.*14_*15insGG
XR_001738751.2:n.2058_2059insGG
XR_001738752.2:n.1880_1881insGG
XR_427087.4:n.1937_1938insGG
NM_006186.4:c.*14_*15insGG MANE Select	NP_006177.1:n.*14_*15insGG
NM_173173.3:c.*14_*15insGG	NP_775265.1:n.*14_*15insGG