Canonical Allele Identifier: CA2661538832

Gene: NR4A2

Linked Data

• gnomAD v4: 2-156325672-CCCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325673_156325675del , CM000664.2:g.156325673_156325675del	GRCh38
NC_000002.11:g.157182185_157182187del , CM000664.1:g.157182185_157182187del	GRCh37
NC_000002.10:g.156890431_156890433del	NCBI36
NG_011821.1:g.12101_12103del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.*69_*71del	ENSP00000514865.1:n.*69_*71del
ENST00000700229.1:c.830_832del
ENST00000700230.1:c.1406_1408del	ENSP00000514867.1:n.1406_1408del
ENST00000700231.1:c.*69_*71del	ENSP00000514868.1:n.*69_*71del
ENST00000339562.9:c.*69_*71del MANE Select	ENSP00000344479.4:n.*69_*71del
ENST00000675870.1:c.*377_*379del	ENSP00000502739.1:n.*377_*379del
ENST00000339562.8:c.*69_*71del	ENSP00000344479.4:n.*69_*71del
ENST00000409572.5:c.*69_*71del	ENSP00000386747.1:n.*69_*71del
ENST00000417764.5:c.*377_*379del	ENSP00000415632.1:n.*377_*379del
ENST00000417972.5:c.*377_*379del	ENSP00000394671.1:n.*377_*379del
ENST00000426264.5:c.*69_*71del	ENSP00000389986.1:n.*69_*71del
NM_006186.3:c.*69_*71del	NP_006177.1:n.*69_*71del
XM_005246621.2:c.*69_*71del	XP_005246678.1:n.*69_*71del
XM_005246622.2:c.*69_*71del	XP_005246679.1:n.*69_*71del
XM_005246623.1:c.*69_*71del	XP_005246680.1:n.*69_*71del
XM_006712553.2:c.*69_*71del	XP_006712616.1:n.*69_*71del
XM_011511246.1:c.*100_*102del	XP_011509548.1:n.*100_*102del
NM_173173.2:c.*69_*71del	NP_775265.1:n.*69_*71del
XM_005246621.4:c.*69_*71del	XP_005246678.1:n.*69_*71del
XM_006712553.4:c.*69_*71del	XP_006712616.1:n.*69_*71del
XM_011511246.2:c.*100_*102del	XP_011509548.1:n.*100_*102del
XM_017004219.2:c.*69_*71del	XP_016859708.1:n.*69_*71del
XM_017004220.2:c.*69_*71del	XP_016859709.1:n.*69_*71del
XR_001738751.2:n.2113_2115del
XR_001738752.2:n.1935_1937del
XR_427087.4:n.1992_1994del
NM_006186.4:c.*69_*71del MANE Select	NP_006177.1:n.*69_*71del
NM_173173.3:c.*69_*71del	NP_775265.1:n.*69_*71del