Canonical Allele Identifier: CA348682752

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157186406T>G (hg19) ; chr2:g.156329894T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329894T>G , CM000664.2:g.156329894T>G	GRCh38
NC_000002.11:g.157186406T>G , CM000664.1:g.157186406T>G	GRCh37
NC_000002.10:g.156894652T>G	NCBI36
NG_011821.1:g.7882A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.104A>C	ENSP00000388120.2:p.His35Pro
ENST00000700228.1:c.164A>C	ENSP00000514865.1:p.His55Pro
ENST00000700231.1:c.293A>C	ENSP00000514868.1:p.His98Pro
ENST00000339562.9:c.293A>C MANE Select	ENSP00000344479.4:p.His98Pro
ENST00000675870.1:c.104A>C	ENSP00000502739.1:p.His35Pro
ENST00000339562.8:c.293A>C	ENSP00000344479.4:p.His98Pro
ENST00000406048.2:c.208+20A>C
ENST00000409108.6:c.293A>C	ENSP00000386993.2:p.His98Pro
ENST00000409572.5:c.293A>C	ENSP00000386747.1:p.His98Pro
ENST00000417764.5:c.104A>C	ENSP00000415632.1:p.His35Pro
ENST00000417972.5:c.104A>C	ENSP00000394671.1:p.His35Pro
ENST00000421709.1:c.104A>C	ENSP00000388120.1:p.His35Pro
ENST00000424077.1:c.293A>C	ENSP00000406808.1:p.His98Pro
ENST00000426264.5:c.104A>C	ENSP00000389986.1:p.His35Pro
ENST00000429376.5:c.104A>C	ENSP00000410952.1:p.His35Pro
NM_006186.3:c.293A>C	NP_006177.1:p.His98Pro
XM_005246621.2:c.326A>C	XP_005246678.1:p.His109Pro
XM_005246622.2:c.104A>C	XP_005246679.1:p.His35Pro
XM_005246623.1:c.104A>C	XP_005246680.1:p.His35Pro
XM_006712553.2:c.326A>C	XP_006712616.1:p.His109Pro
XM_011511246.1:c.326A>C	XP_011509548.1:p.His109Pro
XR_427087.2:n.2499A>C
NM_173173.2:c.104A>C	NP_775265.1:p.His35Pro
XM_005246621.4:c.326A>C	XP_005246678.1:p.His109Pro
XM_006712553.4:c.326A>C	XP_006712616.1:p.His109Pro
XM_011511246.2:c.326A>C	XP_011509548.1:p.His109Pro
XM_017004219.2:c.293A>C	XP_016859708.1:p.His98Pro
XM_017004220.2:c.293A>C	XP_016859709.1:p.His98Pro
XR_001738751.2:n.661A>C
XR_001738752.2:n.483A>C
XR_427087.4:n.540A>C
NM_006186.4:c.293A>C MANE Select	NP_006177.1:p.His98Pro
NM_173173.3:c.104A>C	NP_775265.1:p.His35Pro