Canonical Allele Identifier: CA348681765

Gene: NR4A2

Linked Data

• gnomAD v4: 2-156329436-G-T
• MyVariant Identifiers: chr2:g.157185948G>T (hg19) ; chr2:g.156329436G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329436G>T , CM000664.2:g.156329436G>T	GRCh38
NC_000002.11:g.157185948G>T , CM000664.1:g.157185948G>T	GRCh37
NC_000002.10:g.156894194G>T	NCBI36
NG_011821.1:g.8340C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.622C>A	ENSP00000514865.1:p.Pro208Thr
ENST00000700230.1:c.184C>A	ENSP00000514867.1:p.Pro62Thr
ENST00000700231.1:c.751C>A	ENSP00000514868.1:p.Pro251Thr
ENST00000339562.9:c.751C>A MANE Select	ENSP00000344479.4:p.Pro251Thr
ENST00000675870.1:c.562C>A	ENSP00000502739.1:p.Pro188Thr
ENST00000339562.8:c.751C>A	ENSP00000344479.4:p.Pro251Thr
ENST00000406048.2:c.208+478C>A
ENST00000409108.6:c.751C>A	ENSP00000386993.2:p.Pro251Thr
ENST00000409572.5:c.751C>A	ENSP00000386747.1:p.Pro251Thr
ENST00000417764.5:c.562C>A	ENSP00000415632.1:p.Pro188Thr
ENST00000417972.5:c.562C>A	ENSP00000394671.1:p.Pro188Thr
ENST00000424077.1:c.751C>A	ENSP00000406808.1:p.Pro251Thr
ENST00000426264.5:c.562C>A	ENSP00000389986.1:p.Pro188Thr
ENST00000429376.5:c.562C>A	ENSP00000410952.1:p.Pro188Thr
NM_006186.3:c.751C>A	NP_006177.1:p.Pro251Thr
XM_005246621.2:c.784C>A	XP_005246678.1:p.Pro262Thr
XM_005246622.2:c.562C>A	XP_005246679.1:p.Pro188Thr
XM_005246623.1:c.562C>A	XP_005246680.1:p.Pro188Thr
XM_006712553.2:c.784C>A	XP_006712616.1:p.Pro262Thr
XM_011511246.1:c.784C>A	XP_011509548.1:p.Pro262Thr
XR_427087.2:n.2957C>A
NM_173173.2:c.562C>A	NP_775265.1:p.Pro188Thr
XM_005246621.4:c.784C>A	XP_005246678.1:p.Pro262Thr
XM_006712553.4:c.784C>A	XP_006712616.1:p.Pro262Thr
XM_011511246.2:c.784C>A	XP_011509548.1:p.Pro262Thr
XM_017004219.2:c.751C>A	XP_016859708.1:p.Pro251Thr
XM_017004220.2:c.751C>A	XP_016859709.1:p.Pro251Thr
XR_001738751.2:n.1119C>A
XR_001738752.2:n.941C>A
XR_427087.4:n.998C>A
NM_006186.4:c.751C>A MANE Select	NP_006177.1:p.Pro251Thr
NM_173173.3:c.562C>A	NP_775265.1:p.Pro188Thr