Canonical Allele Identifier: CA2661539675

Gene: NR4A2

Linked Data

• ClinVar Variation Id: 2631914
• ClinVar RCV Id: RCV003414481
• gnomAD v4: 2-156329475-CGAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329476_156329478del , CM000664.2:g.156329476_156329478del	GRCh38
NC_000002.11:g.157185988_157185990del , CM000664.1:g.157185988_157185990del	GRCh37
NC_000002.10:g.156894234_156894236del	NCBI36
NG_011821.1:g.8298_8300del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.580_582del	ENSP00000514865.1:p.Ile194del
ENST00000700230.1:c.142_144del	ENSP00000514867.1:p.Ile48del
ENST00000700231.1:c.709_711del	ENSP00000514868.1:p.Ile237del
ENST00000339562.9:c.709_711del MANE Select	ENSP00000344479.4:p.Ile237del
ENST00000675870.1:c.520_522del	ENSP00000502739.1:p.Ile174del
ENST00000339562.8:c.709_711del	ENSP00000344479.4:p.Ile237del
ENST00000406048.2:c.208+436_208+438del
ENST00000409108.6:c.709_711del	ENSP00000386993.2:p.Ile237del
ENST00000409572.5:c.709_711del	ENSP00000386747.1:p.Ile237del
ENST00000417764.5:c.520_522del	ENSP00000415632.1:p.Ile174del
ENST00000417972.5:c.520_522del	ENSP00000394671.1:p.Ile174del
ENST00000424077.1:c.709_711del	ENSP00000406808.1:p.Ile237del
ENST00000426264.5:c.520_522del	ENSP00000389986.1:p.Ile174del
ENST00000429376.5:c.520_522del	ENSP00000410952.1:p.Ile174del
NM_006186.3:c.709_711del	NP_006177.1:p.Ile237del
XM_005246621.2:c.742_744del	XP_005246678.1:p.Ile248del
XM_005246622.2:c.520_522del	XP_005246679.1:p.Ile174del
XM_005246623.1:c.520_522del	XP_005246680.1:p.Ile174del
XM_006712553.2:c.742_744del	XP_006712616.1:p.Ile248del
XM_011511246.1:c.742_744del	XP_011509548.1:p.Ile248del
XR_427087.2:n.2915_2917del
NM_173173.2:c.520_522del	NP_775265.1:p.Ile174del
XM_005246621.4:c.742_744del	XP_005246678.1:p.Ile248del
XM_006712553.4:c.742_744del	XP_006712616.1:p.Ile248del
XM_011511246.2:c.742_744del	XP_011509548.1:p.Ile248del
XM_017004219.2:c.709_711del	XP_016859708.1:p.Ile237del
XM_017004220.2:c.709_711del	XP_016859709.1:p.Ile237del
XR_001738751.2:n.1077_1079del
XR_001738752.2:n.899_901del
XR_427087.4:n.956_958del
NM_006186.4:c.709_711del MANE Select	NP_006177.1:p.Ile237del
NM_173173.3:c.520_522del	NP_775265.1:p.Ile174del