Canonical Allele Identifier: CA348682056

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157186090G>C (hg19) ; chr2:g.156329578G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329578G>C , CM000664.2:g.156329578G>C	GRCh38
NC_000002.11:g.157186090G>C , CM000664.1:g.157186090G>C	GRCh37
NC_000002.10:g.156894336G>C	NCBI36
NG_011821.1:g.8198C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.420C>G	ENSP00000388120.2:p.Asn140Lys
ENST00000700228.1:c.480C>G	ENSP00000514865.1:p.Asn160Lys
ENST00000700230.1:c.42C>G	ENSP00000514867.1:p.Asn14Lys
ENST00000700231.1:c.609C>G	ENSP00000514868.1:p.Asn203Lys
ENST00000339562.9:c.609C>G MANE Select	ENSP00000344479.4:p.Asn203Lys
ENST00000675870.1:c.420C>G	ENSP00000502739.1:p.Asn140Lys
ENST00000339562.8:c.609C>G	ENSP00000344479.4:p.Asn203Lys
ENST00000406048.2:c.208+336C>G
ENST00000409108.6:c.609C>G	ENSP00000386993.2:p.Asn203Lys
ENST00000409572.5:c.609C>G	ENSP00000386747.1:p.Asn203Lys
ENST00000417764.5:c.420C>G	ENSP00000415632.1:p.Asn140Lys
ENST00000417972.5:c.420C>G	ENSP00000394671.1:p.Asn140Lys
ENST00000424077.1:c.609C>G	ENSP00000406808.1:p.Asn203Lys
ENST00000426264.5:c.420C>G	ENSP00000389986.1:p.Asn140Lys
ENST00000429376.5:c.420C>G	ENSP00000410952.1:p.Asn140Lys
NM_006186.3:c.609C>G	NP_006177.1:p.Asn203Lys
XM_005246621.2:c.642C>G	XP_005246678.1:p.Asn214Lys
XM_005246622.2:c.420C>G	XP_005246679.1:p.Asn140Lys
XM_005246623.1:c.420C>G	XP_005246680.1:p.Asn140Lys
XM_006712553.2:c.642C>G	XP_006712616.1:p.Asn214Lys
XM_011511246.1:c.642C>G	XP_011509548.1:p.Asn214Lys
XR_427087.2:n.2815C>G
NM_173173.2:c.420C>G	NP_775265.1:p.Asn140Lys
XM_005246621.4:c.642C>G	XP_005246678.1:p.Asn214Lys
XM_006712553.4:c.642C>G	XP_006712616.1:p.Asn214Lys
XM_011511246.2:c.642C>G	XP_011509548.1:p.Asn214Lys
XM_017004219.2:c.609C>G	XP_016859708.1:p.Asn203Lys
XM_017004220.2:c.609C>G	XP_016859709.1:p.Asn203Lys
XR_001738751.2:n.977C>G
XR_001738752.2:n.799C>G
XR_427087.4:n.856C>G
NM_006186.4:c.609C>G MANE Select	NP_006177.1:p.Asn203Lys
NM_173173.3:c.420C>G	NP_775265.1:p.Asn140Lys