Canonical Allele Identifier: CA2262900692
Gene: PNPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47946800C= , CM000679.2:g.47946800C= GRCh38
NC_000017.10:g.46024166C= , CM000679.1:g.46024166C= GRCh37
NC_000017.9:g.43379165C= NCBI36
NG_008744.1:g.10278C=

Transcript Alleles

HGVS Amino-acid change
ENST00000225573.5:c.*18C= ENSP00000225573.5:n.*18C=
ENST00000434554.7:c.*18C= ENSP00000399960.3:n.*18C=
ENST00000582171.6:c.*469C= ENSP00000463994.1:n.*469C=
ENST00000584806.2:n.473C=
ENST00000641305.1:n.2303C=
ENST00000641323.1:c.*823C= ENSP00000492965.1:n.*823C=
ENST00000641427.1:n.804C=
ENST00000641703.1:c.520C= ENSP00000493219.1:n.520C=
ENST00000641709.1:c.*626C= ENSP00000493349.1:n.*626C=
ENST00000641856.1:c.*1312C= ENSP00000493224.1:n.*1312C=
ENST00000642017.2:c.*18C= MANE Select ENSP00000493302.2:n.*18C=
ENST00000225573.4:c.*18C= ENSP00000225573.4:n.*18C=
ENST00000434554.6:c.*18C= ENSP00000399960.2:n.*18C=
ENST00000582171.5:c.*469C= ENSP00000463994.1:n.*469C=
ENST00000584806.1:n.473C=
NM_018129.3:c.*18C= NP_060599.1:n.*18C=
XM_005257500.2:c.*18C= XP_005257557.1:n.*18C=
XM_011524968.1:c.*18C= XP_011523270.1:n.*18C=
XM_005257500.3:c.*18C= XP_005257557.1:n.*18C=
XM_011524968.2:c.*18C= XP_011523270.1:n.*18C=
XM_017024813.1:c.*18C= XP_016880302.1:n.*18C=
NM_018129.4:c.*18C= MANE Select NP_060599.1:n.*18C=