Canonical Allele Identifier: CA2262900354
Community Standard Title: NM_018129.4(PNPO):c.542G= (p.Arg181=)
Gene: PNPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47945985G= , CM000679.2:g.47945985G= GRCh38
NC_000017.10:g.46023351G= , CM000679.1:g.46023351G= GRCh37
NC_000017.9:g.43378350G= NCBI36
NG_008744.1:g.9463G=

Transcript Alleles

HGVS Amino-acid Change
NM_018129.4:c.542G= MANE Select NP_060599.1:p.Arg181=
ENST00000642017.2:c.542G= MANE Select ENSP00000493302.2:p.Arg181=
NM_018129.3:c.542G= NP_060599.1:p.Arg181=
ENST00000225573.4:c.542G= ENSP00000225573.4:p.Arg181=
ENST00000225573.5:c.418-338G= ENSP00000225573.5:n.418-338G=
ENST00000434554.6:c.418-338G= ENSP00000399960.2:n.418-338G=
ENST00000434554.7:c.488G= ENSP00000399960.3:p.Arg163=
ENST00000582171.5:c.*207G= ENSP00000463994.1:n.*207G=
ENST00000582171.6:c.*207G= ENSP00000463994.1:n.*207G=
ENST00000583245.5:c.*561G= ENSP00000463520.1:n.*561G=
ENST00000583245.6:n.514G=
ENST00000583599.5:c.302G= ENSP00000463919.1:p.Arg101=
ENST00000583599.6:c.302G= ENSP00000463919.2:p.Arg101=
ENST00000584061.6:c.473G= ENSP00000463972.2:p.Arg158=
ENST00000584806.1:n.216-338G=
ENST00000584806.2:n.216-338G=
ENST00000585320.5:c.*29-338G= ENSP00000462345.1:n.*29-338G=
ENST00000641285.1:n.322G=
ENST00000641305.1:n.1708G=
ENST00000641323.1:c.*561G= ENSP00000492965.1:n.*561G=
ENST00000641427.1:n.542G=
ENST00000641511.1:c.279-338G=
ENST00000641703.1:c.258G= ENSP00000493219.1:n.258G=
ENST00000641709.1:c.*364G= ENSP00000493349.1:n.*364G=
ENST00000641856.1:c.*1050G= ENSP00000493224.1:n.*1050G=
XM_005257500.2:c.302G= XP_005257557.1:p.Arg101=
XM_005257500.3:c.302G= XP_005257557.1:p.Arg101=
XM_011524968.1:c.257G= XP_011523270.1:p.Arg86=
XM_011524968.2:c.257G= XP_011523270.1:p.Arg86=
XM_017024813.1:c.302G= XP_016880302.1:p.Arg101=