Canonical Allele Identifier: CA348679274

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182281A>G (hg19) ; chr2:g.156325769A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325769A>G , CM000664.2:g.156325769A>G	GRCh38
NC_000002.11:g.157182281A>G , CM000664.1:g.157182281A>G	GRCh37
NC_000002.10:g.156890527A>G	NCBI36
NG_011821.1:g.12007T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1568T>C	ENSP00000514865.1:p.Leu523Pro
ENST00000700229.1:c.736T>C
ENST00000700230.1:c.1312T>C	ENSP00000514867.1:n.1312T>C
ENST00000700231.1:c.1697T>C	ENSP00000514868.1:p.Leu566Pro
ENST00000339562.9:c.1772T>C MANE Select	ENSP00000344479.4:p.Leu591Pro
ENST00000675870.1:c.*283T>C	ENSP00000502739.1:n.*283T>C
ENST00000339562.8:c.1772T>C	ENSP00000344479.4:p.Leu591Pro
ENST00000409108.6:c.*6T>C	ENSP00000386993.2:n.*6T>C
ENST00000409572.5:c.1772T>C	ENSP00000386747.1:p.Leu591Pro
ENST00000417764.5:c.*283T>C	ENSP00000415632.1:n.*283T>C
ENST00000417972.5:c.*283T>C	ENSP00000394671.1:n.*283T>C
ENST00000426264.5:c.1583T>C	ENSP00000389986.1:p.Leu528Pro
ENST00000429376.5:c.*6T>C	ENSP00000410952.1:n.*6T>C
NM_006186.3:c.1772T>C	NP_006177.1:p.Leu591Pro
XM_005246621.2:c.1805T>C	XP_005246678.1:p.Leu602Pro
XM_005246622.2:c.1583T>C	XP_005246679.1:p.Leu528Pro
XM_005246623.1:c.1583T>C	XP_005246680.1:p.Leu528Pro
XM_006712553.2:c.1730T>C	XP_006712616.1:p.Leu577Pro
XM_011511246.1:c.*6T>C	XP_011509548.1:n.*6T>C
NM_173173.2:c.1583T>C	NP_775265.1:p.Leu528Pro
XM_005246621.4:c.1805T>C	XP_005246678.1:p.Leu602Pro
XM_006712553.4:c.1730T>C	XP_006712616.1:p.Leu577Pro
XM_011511246.2:c.*6T>C	XP_011509548.1:n.*6T>C
XM_017004219.2:c.1772T>C	XP_016859708.1:p.Leu591Pro
XM_017004220.2:c.1697T>C	XP_016859709.1:p.Leu566Pro
XR_001738751.2:n.2019T>C
XR_001738752.2:n.1841T>C
XR_427087.4:n.1898T>C
NM_006186.4:c.1772T>C MANE Select	NP_006177.1:p.Leu591Pro
NM_173173.3:c.1583T>C	NP_775265.1:p.Leu528Pro