Canonical Allele Identifier: CA2262900704
Gene: PNPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47946829A= , CM000679.2:g.47946829A= GRCh38
NC_000017.10:g.46024195A= , CM000679.1:g.46024195A= GRCh37
NC_000017.9:g.43379194A= NCBI36
NG_008744.1:g.10307A=

Transcript Alleles

HGVS Amino-acid change
ENST00000225573.5:c.*47A= ENSP00000225573.5:n.*47A=
ENST00000434554.7:c.*47A= ENSP00000399960.3:n.*47A=
ENST00000582171.6:c.*498A= ENSP00000463994.1:n.*498A=
ENST00000584806.2:n.502A=
ENST00000641305.1:n.2332A=
ENST00000641323.1:c.*852A= ENSP00000492965.1:n.*852A=
ENST00000641427.1:n.833A=
ENST00000641703.1:c.549A= ENSP00000493219.1:n.549A=
ENST00000641709.1:c.*655A= ENSP00000493349.1:n.*655A=
ENST00000641856.1:c.*1341A= ENSP00000493224.1:n.*1341A=
ENST00000642017.2:c.*47A= MANE Select ENSP00000493302.2:n.*47A=
ENST00000225573.4:c.*47A= ENSP00000225573.4:n.*47A=
ENST00000434554.6:c.*47A= ENSP00000399960.2:n.*47A=
ENST00000582171.5:c.*498A= ENSP00000463994.1:n.*498A=
ENST00000584806.1:n.502A=
NM_018129.3:c.*47A= NP_060599.1:n.*47A=
XM_005257500.2:c.*47A= XP_005257557.1:n.*47A=
XM_011524968.1:c.*47A= XP_011523270.1:n.*47A=
XM_005257500.3:c.*47A= XP_005257557.1:n.*47A=
XM_011524968.2:c.*47A= XP_011523270.1:n.*47A=
XM_017024813.1:c.*47A= XP_016880302.1:n.*47A=
NM_018129.4:c.*47A= MANE Select NP_060599.1:n.*47A=