Canonical Allele Identifier: CA2262900698
Gene: PNPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47946816G= , CM000679.2:g.47946816G= GRCh38
NC_000017.10:g.46024182G= , CM000679.1:g.46024182G= GRCh37
NC_000017.9:g.43379181G= NCBI36
NG_008744.1:g.10294G=

Transcript Alleles

HGVS Amino-acid change
ENST00000225573.5:c.*34G= ENSP00000225573.5:n.*34G=
ENST00000434554.7:c.*34G= ENSP00000399960.3:n.*34G=
ENST00000582171.6:c.*485G= ENSP00000463994.1:n.*485G=
ENST00000584806.2:n.489G=
ENST00000641305.1:n.2319G=
ENST00000641323.1:c.*839G= ENSP00000492965.1:n.*839G=
ENST00000641427.1:n.820G=
ENST00000641703.1:c.536G= ENSP00000493219.1:n.536G=
ENST00000641709.1:c.*642G= ENSP00000493349.1:n.*642G=
ENST00000641856.1:c.*1328G= ENSP00000493224.1:n.*1328G=
ENST00000642017.2:c.*34G= MANE Select ENSP00000493302.2:n.*34G=
ENST00000225573.4:c.*34G= ENSP00000225573.4:n.*34G=
ENST00000434554.6:c.*34G= ENSP00000399960.2:n.*34G=
ENST00000582171.5:c.*485G= ENSP00000463994.1:n.*485G=
ENST00000584806.1:n.489G=
NM_018129.3:c.*34G= NP_060599.1:n.*34G=
XM_005257500.2:c.*34G= XP_005257557.1:n.*34G=
XM_011524968.1:c.*34G= XP_011523270.1:n.*34G=
XM_005257500.3:c.*34G= XP_005257557.1:n.*34G=
XM_011524968.2:c.*34G= XP_011523270.1:n.*34G=
XM_017024813.1:c.*34G= XP_016880302.1:n.*34G=
NM_018129.4:c.*34G= MANE Select NP_060599.1:n.*34G=