Canonical Allele Identifier: CA2837995531
Gene: NR4A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156326222_156330699del , CM000664.2:g.156326222_156330699del GRCh38
NC_000002.11:g.157182734_157187211del , CM000664.1:g.157182734_157187211del GRCh37
NC_000002.10:g.156890980_156895457del NCBI36
NG_011821.1:g.7077_11554del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700228.1:c.-146_1264del
ENST00000700231.1:c.-34_1393del
ENST00000339562.9:c.-34_1468del
ENST00000675870.1:c.-45_1173-15del
ENST00000339562.8:c.-34_1468del
ENST00000409108.6:c.-34_1379-15del
ENST00000409572.5:c.-34_1468del
ENST00000417764.5:c.-45_1173-15del
ENST00000417972.5:c.-45_1173-15del
ENST00000426264.5:c.-45_1279del
ENST00000429376.5:c.-45_1190-15del
NM_006186.3:c.-34_1468del
XM_005246621.2:c.32-511_1501del
XM_005246622.2:c.-45_1279del
XM_005246623.1:c.-13-689_1279del
XM_006712553.2:c.32-511_1426del
XM_011511246.1:c.32-511_1412-15del
XR_427087.2:n.2205-511_3568-15del
NM_173173.2:c.-45_1279del
XM_005246621.4:c.32-511_1501del
XM_006712553.4:c.32-511_1426del
XM_011511246.2:c.32-511_1412-15del
XM_017004219.2:c.-34_1468del
XM_017004220.2:c.-34_1393del
XR_001738751.2:n.335_1730-15del
XR_001738752.2:n.335_1552-15del
XR_427087.4:n.246-511_1609-15del
NM_006186.4:c.-34_1468del
NM_173173.3:c.-45_1279del