Canonical Allele Identifier: CA2262900712
Gene: PNPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47946848C= , CM000679.2:g.47946848C= GRCh38
NC_000017.10:g.46024214C= , CM000679.1:g.46024214C= GRCh37
NC_000017.9:g.43379213C= NCBI36
NG_008744.1:g.10326C=

Transcript Alleles

HGVS Amino-acid change
ENST00000225573.5:c.*66C= ENSP00000225573.5:n.*66C=
ENST00000434554.7:c.*66C= ENSP00000399960.3:n.*66C=
ENST00000582171.6:c.*517C= ENSP00000463994.1:n.*517C=
ENST00000584806.2:n.521C=
ENST00000641305.1:n.2351C=
ENST00000641323.1:c.*871C= ENSP00000492965.1:n.*871C=
ENST00000641427.1:n.852C=
ENST00000641703.1:c.568C= ENSP00000493219.1:n.568C=
ENST00000641709.1:c.*674C= ENSP00000493349.1:n.*674C=
ENST00000641856.1:c.*1360C= ENSP00000493224.1:n.*1360C=
ENST00000642017.2:c.*66C= MANE Select ENSP00000493302.2:n.*66C=
ENST00000225573.4:c.*66C= ENSP00000225573.4:n.*66C=
ENST00000434554.6:c.*66C= ENSP00000399960.2:n.*66C=
ENST00000582171.5:c.*517C= ENSP00000463994.1:n.*517C=
ENST00000584806.1:n.521C=
NM_018129.3:c.*66C= NP_060599.1:n.*66C=
XM_005257500.2:c.*66C= XP_005257557.1:n.*66C=
XM_011524968.1:c.*66C= XP_011523270.1:n.*66C=
XM_005257500.3:c.*66C= XP_005257557.1:n.*66C=
XM_011524968.2:c.*66C= XP_011523270.1:n.*66C=
XM_017024813.1:c.*66C= XP_016880302.1:n.*66C=
NM_018129.4:c.*66C= MANE Select NP_060599.1:n.*66C=