Canonical Allele Identifier: CA59155141
Gene: NR4A2 HGNC NCBI

Linked Data

dbSNP Id: rs35100271

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156330038dup , CM000664.2:g.156330038dup GRCh38
NC_000002.11:g.157186550dup , CM000664.1:g.157186550dup GRCh37
NC_000002.10:g.156894796dup NCBI36
NG_011821.1:g.7740dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000421709.2:c.-13-26dup ENSP00000388120.2:n.-13-26dup
ENST00000700228.1:c.22dup ENSP00000514865.1:p.Ile8AsnfsTer?
ENST00000700231.1:c.151dup ENSP00000514868.1:p.Ile51AsnfsTer?
ENST00000339562.9:c.151dup MANE Select ENSP00000344479.4:p.Ile51AsnfsTer?
ENST00000675870.1:c.-13-26dup ENSP00000502739.1:n.-13-26dup
ENST00000339562.8:c.151dup ENSP00000344479.4:p.Ile51AsnfsTer?
ENST00000406048.2:c.86dup
ENST00000409108.6:c.151dup ENSP00000386993.2:p.Ile51AsnfsTer?
ENST00000409572.5:c.151dup ENSP00000386747.1:p.Ile51AsnfsTer?
ENST00000417764.5:c.-13-26dup ENSP00000415632.1:n.-13-26dup
ENST00000417972.5:c.-13-26dup ENSP00000394671.1:n.-13-26dup
ENST00000421709.1:c.-13-26dup ENSP00000388120.1:n.-13-26dup
ENST00000424077.1:c.151dup ENSP00000406808.1:p.Ile51AsnfsTer?
ENST00000426264.5:c.-13-26dup ENSP00000389986.1:n.-13-26dup
ENST00000429376.5:c.-13-26dup ENSP00000410952.1:n.-13-26dup
NM_006186.3:c.151dup NP_006177.1:p.Ile51AsnfsTer?
XM_005246621.2:c.184dup XP_005246678.1:p.Ile62AsnfsTer?
XM_005246622.2:c.-13-26dup XP_005246679.1:n.-13-26dup
XM_005246623.1:c.-13-26dup XP_005246680.1:n.-13-26dup
XM_006712553.2:c.184dup XP_006712616.1:p.Ile62AsnfsTer?
XM_011511246.1:c.184dup XP_011509548.1:p.Ile62AsnfsTer?
XR_427087.2:n.2357dup
NM_173173.2:c.-13-26dup NP_775265.1:n.-13-26dup
XM_005246621.4:c.184dup XP_005246678.1:p.Ile62AsnfsTer?
XM_006712553.4:c.184dup XP_006712616.1:p.Ile62AsnfsTer?
XM_011511246.2:c.184dup XP_011509548.1:p.Ile62AsnfsTer?
XM_017004219.2:c.151dup XP_016859708.1:p.Ile51AsnfsTer?
XM_017004220.2:c.151dup XP_016859709.1:p.Ile51AsnfsTer?
XR_001738751.2:n.519dup
XR_001738752.2:n.367-26dup
XR_427087.4:n.398dup
NM_006186.4:c.151dup MANE Select NP_006177.1:p.Ile51AsnfsTer?
NM_173173.3:c.-13-26dup NP_775265.1:n.-13-26dup