Canonical Allele Identifier: CA537508954

Gene: NR4A2

Linked Data

• dbSNP Id: rs1407445227
• gnomAD v2: 2-157186226-GCCA-G
• gnomAD v4: 2-156329714-GCCA-G
• MyVariant Identifiers: chr2:g.157186227_157186229del (hg19) ; chr2:g.156329715_156329717del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329716_156329718del , CM000664.2:g.156329716_156329718del	GRCh38
NC_000002.11:g.157186228_157186230del , CM000664.1:g.157186228_157186230del	GRCh37
NC_000002.10:g.156894474_156894476del	NCBI36
NG_011821.1:g.8059_8061del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.281_283del	ENSP00000388120.2:p.Val94del
ENST00000700228.1:c.341_343del	ENSP00000514865.1:p.Val114del
ENST00000700231.1:c.470_472del	ENSP00000514868.1:p.Val157del
ENST00000339562.9:c.470_472del MANE Select	ENSP00000344479.4:p.Val157del
ENST00000675870.1:c.281_283del	ENSP00000502739.1:p.Val94del
ENST00000339562.8:c.470_472del	ENSP00000344479.4:p.Val157del
ENST00000406048.2:c.208+197_208+199del
ENST00000409108.6:c.470_472del	ENSP00000386993.2:p.Val157del
ENST00000409572.5:c.470_472del	ENSP00000386747.1:p.Val157del
ENST00000417764.5:c.281_283del	ENSP00000415632.1:p.Val94del
ENST00000417972.5:c.281_283del	ENSP00000394671.1:p.Val94del
ENST00000421709.1:c.281_283del	ENSP00000388120.1:p.Val94del
ENST00000424077.1:c.470_472del	ENSP00000406808.1:p.Val157del
ENST00000426264.5:c.281_283del	ENSP00000389986.1:p.Val94del
ENST00000429376.5:c.281_283del	ENSP00000410952.1:p.Val94del
NM_006186.3:c.470_472del	NP_006177.1:p.Val157del
XM_005246621.2:c.503_505del	XP_005246678.1:p.Val168del
XM_005246622.2:c.281_283del	XP_005246679.1:p.Val94del
XM_005246623.1:c.281_283del	XP_005246680.1:p.Val94del
XM_006712553.2:c.503_505del	XP_006712616.1:p.Val168del
XM_011511246.1:c.503_505del	XP_011509548.1:p.Val168del
XR_427087.2:n.2676_2678del
NM_173173.2:c.281_283del	NP_775265.1:p.Val94del
XM_005246621.4:c.503_505del	XP_005246678.1:p.Val168del
XM_006712553.4:c.503_505del	XP_006712616.1:p.Val168del
XM_011511246.2:c.503_505del	XP_011509548.1:p.Val168del
XM_017004219.2:c.470_472del	XP_016859708.1:p.Val157del
XM_017004220.2:c.470_472del	XP_016859709.1:p.Val157del
XR_001738751.2:n.838_840del
XR_001738752.2:n.660_662del
XR_427087.4:n.717_719del
NM_006186.4:c.470_472del MANE Select	NP_006177.1:p.Val157del
NM_173173.3:c.281_283del	NP_775265.1:p.Val94del