Canonical Allele Identifier: CA1916163

Gene: NR4A2

Linked Data

• dbSNP Id: rs758074547
• ExAC: 2:157182376 G / C
• gnomAD v2: 2-157182376-G-C
• gnomAD v4: 2-156325864-G-C
• MyVariant Identifiers: chr2:g.157182376G>C (hg19) ; chr2:g.156325864G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325864G>C , CM000664.2:g.156325864G>C	GRCh38
NC_000002.11:g.157182376G>C , CM000664.1:g.157182376G>C	GRCh37
NC_000002.10:g.156890622G>C	NCBI36
NG_011821.1:g.11912C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1473C>G	ENSP00000514865.1:p.Leu491=
ENST00000700229.1:c.641C>G
ENST00000700230.1:c.1217C>G	ENSP00000514867.1:n.1217C>G
ENST00000700231.1:c.1602C>G	ENSP00000514868.1:p.Leu534=
ENST00000339562.9:c.1677C>G MANE Select	ENSP00000344479.4:p.Leu559=
ENST00000675870.1:c.*188C>G	ENSP00000502739.1:n.*188C>G
ENST00000339562.8:c.1677C>G	ENSP00000344479.4:p.Leu559=
ENST00000409108.6:c.1573C>G	ENSP00000386993.2:p.Pro525Ala
ENST00000409572.5:c.1677C>G	ENSP00000386747.1:p.Leu559=
ENST00000417764.5:c.*188C>G	ENSP00000415632.1:n.*188C>G
ENST00000417972.5:c.*188C>G	ENSP00000394671.1:n.*188C>G
ENST00000426264.5:c.1488C>G	ENSP00000389986.1:p.Leu496=
ENST00000429376.5:c.1384C>G	ENSP00000410952.1:p.Pro462Ala
NM_006186.3:c.1677C>G	NP_006177.1:p.Leu559=
XM_005246621.2:c.1710C>G	XP_005246678.1:p.Leu570=
XM_005246622.2:c.1488C>G	XP_005246679.1:p.Leu496=
XM_005246623.1:c.1488C>G	XP_005246680.1:p.Leu496=
XM_006712553.2:c.1635C>G	XP_006712616.1:p.Leu545=
XM_011511246.1:c.1606C>G	XP_011509548.1:p.Pro536Ala
NM_173173.2:c.1488C>G	NP_775265.1:p.Leu496=
XM_005246621.4:c.1710C>G	XP_005246678.1:p.Leu570=
XM_006712553.4:c.1635C>G	XP_006712616.1:p.Leu545=
XM_011511246.2:c.1606C>G	XP_011509548.1:p.Pro536Ala
XM_017004219.2:c.1677C>G	XP_016859708.1:p.Leu559=
XM_017004220.2:c.1602C>G	XP_016859709.1:p.Leu534=
XR_001738751.2:n.1924C>G
XR_001738752.2:n.1746C>G
XR_427087.4:n.1803C>G
NM_006186.4:c.1677C>G MANE Select	NP_006177.1:p.Leu559=
NM_173173.3:c.1488C>G	NP_775265.1:p.Leu496=