Canonical Allele Identifier: CA348680024

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182697G>T (hg19) ; chr2:g.156326185G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326185G>T , CM000664.2:g.156326185G>T	GRCh38
NC_000002.11:g.157182697G>T , CM000664.1:g.157182697G>T	GRCh37
NC_000002.10:g.156890943G>T	NCBI36
NG_011821.1:g.11591C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1301C>A	ENSP00000514865.1:p.Ala434Asp
ENST00000700229.1:c.469C>A
ENST00000700230.1:c.1045C>A	ENSP00000514867.1:n.1045C>A
ENST00000700231.1:c.1430C>A	ENSP00000514868.1:p.Ala477Asp
ENST00000339562.9:c.1505C>A MANE Select	ENSP00000344479.4:p.Ala502Asp
ENST00000675870.1:c.*16C>A	ENSP00000502739.1:n.*16C>A
ENST00000339562.8:c.1505C>A	ENSP00000344479.4:p.Ala502Asp
ENST00000409108.6:c.1401C>A	ENSP00000386993.2:p.Cys467Ter
ENST00000409572.5:c.1505C>A	ENSP00000386747.1:p.Ala502Asp
ENST00000417764.5:c.*16C>A	ENSP00000415632.1:n.*16C>A
ENST00000417972.5:c.*16C>A	ENSP00000394671.1:n.*16C>A
ENST00000426264.5:c.1316C>A	ENSP00000389986.1:p.Ala439Asp
ENST00000429376.5:c.1212C>A	ENSP00000410952.1:p.Cys404Ter
NM_006186.3:c.1505C>A	NP_006177.1:p.Ala502Asp
XM_005246621.2:c.1538C>A	XP_005246678.1:p.Ala513Asp
XM_005246622.2:c.1316C>A	XP_005246679.1:p.Ala439Asp
XM_005246623.1:c.1316C>A	XP_005246680.1:p.Ala439Asp
XM_006712553.2:c.1463C>A	XP_006712616.1:p.Ala488Asp
XM_011511246.1:c.1434C>A	XP_011509548.1:p.Cys478Ter
XR_427087.2:n.3590C>A
NM_173173.2:c.1316C>A	NP_775265.1:p.Ala439Asp
XM_005246621.4:c.1538C>A	XP_005246678.1:p.Ala513Asp
XM_006712553.4:c.1463C>A	XP_006712616.1:p.Ala488Asp
XM_011511246.2:c.1434C>A	XP_011509548.1:p.Cys478Ter
XM_017004219.2:c.1505C>A	XP_016859708.1:p.Ala502Asp
XM_017004220.2:c.1430C>A	XP_016859709.1:p.Ala477Asp
XR_001738751.2:n.1752C>A
XR_001738752.2:n.1574C>A
XR_427087.4:n.1631C>A
NM_006186.4:c.1505C>A MANE Select	NP_006177.1:p.Ala502Asp
NM_173173.3:c.1316C>A	NP_775265.1:p.Ala439Asp