Canonical Allele Identifier: CA348679946

Gene: NR4A2

Linked Data

• gnomAD v4: 2-156326156-C-G
• MyVariant Identifiers: chr2:g.157182668C>G (hg19) ; chr2:g.156326156C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326156C>G , CM000664.2:g.156326156C>G	GRCh38
NC_000002.11:g.157182668C>G , CM000664.1:g.157182668C>G	GRCh37
NC_000002.10:g.156890914C>G	NCBI36
NG_011821.1:g.11620G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1330G>C	ENSP00000514865.1:p.Val444Leu
ENST00000700229.1:c.498G>C
ENST00000700230.1:c.1074G>C	ENSP00000514867.1:n.1074G>C
ENST00000700231.1:c.1459G>C	ENSP00000514868.1:p.Val487Leu
ENST00000339562.9:c.1534G>C MANE Select	ENSP00000344479.4:p.Val512Leu
ENST00000675870.1:c.*45G>C	ENSP00000502739.1:n.*45G>C
ENST00000339562.8:c.1534G>C	ENSP00000344479.4:p.Val512Leu
ENST00000409108.6:c.1430G>C	ENSP00000386993.2:p.Gly477Ala
ENST00000409572.5:c.1534G>C	ENSP00000386747.1:p.Val512Leu
ENST00000417764.5:c.*45G>C	ENSP00000415632.1:n.*45G>C
ENST00000417972.5:c.*45G>C	ENSP00000394671.1:n.*45G>C
ENST00000426264.5:c.1345G>C	ENSP00000389986.1:p.Val449Leu
ENST00000429376.5:c.1241G>C	ENSP00000410952.1:p.Gly414Ala
NM_006186.3:c.1534G>C	NP_006177.1:p.Val512Leu
XM_005246621.2:c.1567G>C	XP_005246678.1:p.Val523Leu
XM_005246622.2:c.1345G>C	XP_005246679.1:p.Val449Leu
XM_005246623.1:c.1345G>C	XP_005246680.1:p.Val449Leu
XM_006712553.2:c.1492G>C	XP_006712616.1:p.Val498Leu
XM_011511246.1:c.1463G>C	XP_011509548.1:p.Gly488Ala
XR_427087.2:n.3619G>C
NM_173173.2:c.1345G>C	NP_775265.1:p.Val449Leu
XM_005246621.4:c.1567G>C	XP_005246678.1:p.Val523Leu
XM_006712553.4:c.1492G>C	XP_006712616.1:p.Val498Leu
XM_011511246.2:c.1463G>C	XP_011509548.1:p.Gly488Ala
XM_017004219.2:c.1534G>C	XP_016859708.1:p.Val512Leu
XM_017004220.2:c.1459G>C	XP_016859709.1:p.Val487Leu
XR_001738751.2:n.1781G>C
XR_001738752.2:n.1603G>C
XR_427087.4:n.1660G>C
NM_006186.4:c.1534G>C MANE Select	NP_006177.1:p.Val512Leu
NM_173173.3:c.1345G>C	NP_775265.1:p.Val449Leu