Canonical Allele Identifier: CA1300458814

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325623_156325624delinsCA , CM000664.2:g.156325623_156325624delinsCA	GRCh38
NC_000002.11:g.157182135_157182136delinsCA , CM000664.1:g.157182135_157182136delinsCA	GRCh37
NC_000002.10:g.156890381_156890382delinsCA	NCBI36
NG_011821.1:g.12152_12153delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.*120_*121delinsTG	ENSP00000514865.1:n.*120_*121delinsTG
ENST00000700229.1:c.881_882delinsTG
ENST00000700230.1:c.1457_1458delinsTG	ENSP00000514867.1:n.1457_1458delinsTG
ENST00000700231.1:c.*120_*121delinsTG	ENSP00000514868.1:n.*120_*121delinsTG
ENST00000339562.9:c.*120_*121delinsTG MANE Select	ENSP00000344479.4:n.*120_*121delinsTG
ENST00000675870.1:c.*428_*429delinsTG	ENSP00000502739.1:n.*428_*429delinsTG
ENST00000339562.8:c.*120_*121delinsTG	ENSP00000344479.4:n.*120_*121delinsTG
ENST00000409572.5:c.*120_*121delinsTG	ENSP00000386747.1:n.*120_*121delinsTG
ENST00000417764.5:c.*428_*429delinsTG	ENSP00000415632.1:n.*428_*429delinsTG
ENST00000417972.5:c.*428_*429delinsTG	ENSP00000394671.1:n.*428_*429delinsTG
ENST00000426264.5:c.*120_*121delinsTG	ENSP00000389986.1:n.*120_*121delinsTG
NM_006186.3:c.*120_*121delinsTG	NP_006177.1:n.*120_*121delinsTG
XM_005246621.2:c.*120_*121delinsTG	XP_005246678.1:n.*120_*121delinsTG
XM_005246622.2:c.*120_*121delinsTG	XP_005246679.1:n.*120_*121delinsTG
XM_005246623.1:c.*120_*121delinsTG	XP_005246680.1:n.*120_*121delinsTG
XM_006712553.2:c.*120_*121delinsTG	XP_006712616.1:n.*120_*121delinsTG
XM_011511246.1:c.*151_*152delinsTG	XP_011509548.1:n.*151_*152delinsTG
NM_173173.2:c.*120_*121delinsTG	NP_775265.1:n.*120_*121delinsTG
XM_005246621.4:c.*120_*121delinsTG	XP_005246678.1:n.*120_*121delinsTG
XM_006712553.4:c.*120_*121delinsTG	XP_006712616.1:n.*120_*121delinsTG
XM_011511246.2:c.*151_*152delinsTG	XP_011509548.1:n.*151_*152delinsTG
XM_017004219.2:c.*120_*121delinsTG	XP_016859708.1:n.*120_*121delinsTG
XM_017004220.2:c.*120_*121delinsTG	XP_016859709.1:n.*120_*121delinsTG
XR_001738751.2:n.2164_2165delinsTG
XR_001738752.2:n.1986_1987delinsTG
XR_427087.4:n.2043_2044delinsTG
NM_006186.4:c.*120_*121delinsTG MANE Select	NP_006177.1:n.*120_*121delinsTG
NM_173173.3:c.*120_*121delinsTG	NP_775265.1:n.*120_*121delinsTG