Canonical Allele Identifier: CA2837995540

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326087_156327005del , CM000664.2:g.156326087_156327005del	GRCh38
NC_000002.11:g.157182599_157183517del , CM000664.1:g.157182599_157183517del	GRCh37
NC_000002.10:g.156890845_156891763del	NCBI36
NG_011821.1:g.10775_11693del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.955-81_1336+67del
ENST00000700229.1:c.177-81_504+67del
ENST00000700230.1:c.699-81_1080+67del
ENST00000700231.1:c.1084-81_1465+67del
ENST00000339562.9:c.1159-81_1540+67del
ENST00000675870.1:c.970-81_*51+67del
ENST00000339562.8:c.1159-81_1540+67del
ENST00000409108.6:c.1159-81_1436+67del
ENST00000409572.5:c.1159-81_1540+67del
ENST00000417764.5:c.970-81_*51+67del
ENST00000417972.5:c.970-81_*51+67del
ENST00000426264.5:c.970-81_1351+67del
ENST00000429376.5:c.970-81_1247+67del
NM_006186.3:c.1159-81_1540+67del
XM_005246621.2:c.1192-81_1573+67del
XM_005246622.2:c.970-81_1351+67del
XM_005246623.1:c.970-81_1351+67del
XM_006712553.2:c.1117-81_1498+67del
XM_011511246.1:c.1192-81_1469+67del
XR_427087.2:n.3365-81_3625+67del
NM_173173.2:c.970-81_1351+67del
XM_005246621.4:c.1192-81_1573+67del
XM_006712553.4:c.1117-81_1498+67del
XM_011511246.2:c.1192-81_1469+67del
XM_017004219.2:c.1159-81_1540+67del
XM_017004220.2:c.1084-81_1465+67del
XR_001738751.2:n.1527-81_1787+67del
XR_001738752.2:n.1349-81_1609+67del
XR_427087.4:n.1406-81_1666+67del
NM_006186.4:c.1159-81_1540+67del
NM_173173.3:c.970-81_1351+67del