Canonical Allele Identifier: CA348679952

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182670A>T (hg19) ; chr2:g.156326158A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326158A>T , CM000664.2:g.156326158A>T	GRCh38
NC_000002.11:g.157182670A>T , CM000664.1:g.157182670A>T	GRCh37
NC_000002.10:g.156890916A>T	NCBI36
NG_011821.1:g.11618T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1328T>A	ENSP00000514865.1:p.Met443Lys
ENST00000700229.1:c.496T>A
ENST00000700230.1:c.1072T>A	ENSP00000514867.1:n.1072T>A
ENST00000700231.1:c.1457T>A	ENSP00000514868.1:p.Met486Lys
ENST00000339562.9:c.1532T>A MANE Select	ENSP00000344479.4:p.Met511Lys
ENST00000675870.1:c.*43T>A	ENSP00000502739.1:n.*43T>A
ENST00000339562.8:c.1532T>A	ENSP00000344479.4:p.Met511Lys
ENST00000409108.6:c.1428T>A	ENSP00000386993.2:p.Tyr476Ter
ENST00000409572.5:c.1532T>A	ENSP00000386747.1:p.Met511Lys
ENST00000417764.5:c.*43T>A	ENSP00000415632.1:n.*43T>A
ENST00000417972.5:c.*43T>A	ENSP00000394671.1:n.*43T>A
ENST00000426264.5:c.1343T>A	ENSP00000389986.1:p.Met448Lys
ENST00000429376.5:c.1239T>A	ENSP00000410952.1:p.Tyr413Ter
NM_006186.3:c.1532T>A	NP_006177.1:p.Met511Lys
XM_005246621.2:c.1565T>A	XP_005246678.1:p.Met522Lys
XM_005246622.2:c.1343T>A	XP_005246679.1:p.Met448Lys
XM_005246623.1:c.1343T>A	XP_005246680.1:p.Met448Lys
XM_006712553.2:c.1490T>A	XP_006712616.1:p.Met497Lys
XM_011511246.1:c.1461T>A	XP_011509548.1:p.Tyr487Ter
XR_427087.2:n.3617T>A
NM_173173.2:c.1343T>A	NP_775265.1:p.Met448Lys
XM_005246621.4:c.1565T>A	XP_005246678.1:p.Met522Lys
XM_006712553.4:c.1490T>A	XP_006712616.1:p.Met497Lys
XM_011511246.2:c.1461T>A	XP_011509548.1:p.Tyr487Ter
XM_017004219.2:c.1532T>A	XP_016859708.1:p.Met511Lys
XM_017004220.2:c.1457T>A	XP_016859709.1:p.Met486Lys
XR_001738751.2:n.1779T>A
XR_001738752.2:n.1601T>A
XR_427087.4:n.1658T>A
NM_006186.4:c.1532T>A MANE Select	NP_006177.1:p.Met511Lys
NM_173173.3:c.1343T>A	NP_775265.1:p.Met448Lys