Canonical Allele Identifier: CA2838010100

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326153_156326923del , CM000664.2:g.156326153_156326923del	GRCh38
NC_000002.11:g.157182665_157183435del , CM000664.1:g.157182665_157183435del	GRCh37
NC_000002.10:g.156890911_156891681del	NCBI36
NG_011821.1:g.10856_11626del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.955_1336del
ENST00000700229.1:c.177_504del
ENST00000700230.1:c.699_1080del
ENST00000700231.1:c.1084_1465del
ENST00000339562.9:c.1159_1540del
ENST00000675870.1:c.970_*51del
ENST00000339562.8:c.1159_1540del
ENST00000409108.6:c.1159_1436del
ENST00000409572.5:c.1159_1540del
ENST00000417764.5:c.970_*51del
ENST00000417972.5:c.970_*51del
ENST00000426264.5:c.970_1351del
ENST00000429376.5:c.970_1247del
NM_006186.3:c.1159_1540del
XM_005246621.2:c.1192_1573del
XM_005246622.2:c.970_1351del
XM_005246623.1:c.970_1351del
XM_006712553.2:c.1117_1498del
XM_011511246.1:c.1192_1469del
XR_427087.2:n.3365_3625del
NM_173173.2:c.970_1351del
XM_005246621.4:c.1192_1573del
XM_006712553.4:c.1117_1498del
XM_011511246.2:c.1192_1469del
XM_017004219.2:c.1159_1540del
XM_017004220.2:c.1084_1465del
XR_001738751.2:n.1527_1787del
XR_001738752.2:n.1349_1609del
XR_427087.4:n.1406_1666del
NM_006186.4:c.1159_1540del
NM_173173.3:c.970_1351del