Canonical Allele Identifier: CA759313861

Gene: NR4A2

Linked Data

• dbSNP Id: rs1440881931
• MyVariant Identifiers: chr2:g.157182638del (hg19) ; chr2:g.156326126del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326126del , CM000664.2:g.156326126del	GRCh38
NC_000002.11:g.157182638del , CM000664.1:g.157182638del	GRCh37
NC_000002.10:g.156890884del	NCBI36
NG_011821.1:g.11650del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1336+24del	ENSP00000514865.1:n.1336+24del
ENST00000700229.1:c.504+24del
ENST00000700230.1:c.1080+24del	ENSP00000514867.1:n.1080+24del
ENST00000700231.1:c.1465+24del	ENSP00000514868.1:n.1465+24del
ENST00000339562.9:c.1540+24del MANE Select	ENSP00000344479.4:n.1540+24del
ENST00000675870.1:c.*51+24del	ENSP00000502739.1:n.*51+24del
ENST00000339562.8:c.1540+24del	ENSP00000344479.4:n.1540+24del
ENST00000409108.6:c.1436+24del	ENSP00000386993.2:n.1436+24del
ENST00000409572.5:c.1540+24del	ENSP00000386747.1:n.1540+24del
ENST00000417764.5:c.*51+24del	ENSP00000415632.1:n.*51+24del
ENST00000417972.5:c.*51+24del	ENSP00000394671.1:n.*51+24del
ENST00000426264.5:c.1351+24del	ENSP00000389986.1:n.1351+24del
ENST00000429376.5:c.1247+24del	ENSP00000410952.1:n.1247+24del
NM_006186.3:c.1540+24del	NP_006177.1:n.1540+24del
XM_005246621.2:c.1573+24del	XP_005246678.1:n.1573+24del
XM_005246622.2:c.1351+24del	XP_005246679.1:n.1351+24del
XM_005246623.1:c.1351+24del	XP_005246680.1:n.1351+24del
XM_006712553.2:c.1498+24del	XP_006712616.1:n.1498+24del
XM_011511246.1:c.1469+24del	XP_011509548.1:n.1469+24del
XR_427087.2:n.3625+24del
NM_173173.2:c.1351+24del	NP_775265.1:n.1351+24del
XM_005246621.4:c.1573+24del	XP_005246678.1:n.1573+24del
XM_006712553.4:c.1498+24del	XP_006712616.1:n.1498+24del
XM_011511246.2:c.1469+24del	XP_011509548.1:n.1469+24del
XM_017004219.2:c.1540+24del	XP_016859708.1:n.1540+24del
XM_017004220.2:c.1465+24del	XP_016859709.1:n.1465+24del
XR_001738751.2:n.1787+24del
XR_001738752.2:n.1609+24del
XR_427087.4:n.1666+24del
NM_006186.4:c.1540+24del MANE Select	NP_006177.1:n.1540+24del
NM_173173.3:c.1351+24del	NP_775265.1:n.1351+24del