Canonical Allele Identifier: CA348679954

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182671T>G (hg19) ; chr2:g.156326159T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326159T>G , CM000664.2:g.156326159T>G	GRCh38
NC_000002.11:g.157182671T>G , CM000664.1:g.157182671T>G	GRCh37
NC_000002.10:g.156890917T>G	NCBI36
NG_011821.1:g.11617A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1327A>C	ENSP00000514865.1:p.Met443Leu
ENST00000700229.1:c.495A>C
ENST00000700230.1:c.1071A>C	ENSP00000514867.1:n.1071A>C
ENST00000700231.1:c.1456A>C	ENSP00000514868.1:p.Met486Leu
ENST00000339562.9:c.1531A>C MANE Select	ENSP00000344479.4:p.Met511Leu
ENST00000675870.1:c.*42A>C	ENSP00000502739.1:n.*42A>C
ENST00000339562.8:c.1531A>C	ENSP00000344479.4:p.Met511Leu
ENST00000409108.6:c.1427A>C	ENSP00000386993.2:p.Tyr476Ser
ENST00000409572.5:c.1531A>C	ENSP00000386747.1:p.Met511Leu
ENST00000417764.5:c.*42A>C	ENSP00000415632.1:n.*42A>C
ENST00000417972.5:c.*42A>C	ENSP00000394671.1:n.*42A>C
ENST00000426264.5:c.1342A>C	ENSP00000389986.1:p.Met448Leu
ENST00000429376.5:c.1238A>C	ENSP00000410952.1:p.Tyr413Ser
NM_006186.3:c.1531A>C	NP_006177.1:p.Met511Leu
XM_005246621.2:c.1564A>C	XP_005246678.1:p.Met522Leu
XM_005246622.2:c.1342A>C	XP_005246679.1:p.Met448Leu
XM_005246623.1:c.1342A>C	XP_005246680.1:p.Met448Leu
XM_006712553.2:c.1489A>C	XP_006712616.1:p.Met497Leu
XM_011511246.1:c.1460A>C	XP_011509548.1:p.Tyr487Ser
XR_427087.2:n.3616A>C
NM_173173.2:c.1342A>C	NP_775265.1:p.Met448Leu
XM_005246621.4:c.1564A>C	XP_005246678.1:p.Met522Leu
XM_006712553.4:c.1489A>C	XP_006712616.1:p.Met497Leu
XM_011511246.2:c.1460A>C	XP_011509548.1:p.Tyr487Ser
XM_017004219.2:c.1531A>C	XP_016859708.1:p.Met511Leu
XM_017004220.2:c.1456A>C	XP_016859709.1:p.Met486Leu
XR_001738751.2:n.1778A>C
XR_001738752.2:n.1600A>C
XR_427087.4:n.1657A>C
NM_006186.4:c.1531A>C MANE Select	NP_006177.1:p.Met511Leu
NM_173173.3:c.1342A>C	NP_775265.1:p.Met448Leu