Canonical Allele Identifier: CA291297372

Gene: PNPO

Linked Data

• dbSNP Id: rs1014335830
• gnomAD v4: 17-47946876-A-T
• MyVariant Identifiers: chr17:g.46024242A>T (hg19) ; chr17:g.47946876A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47946876A>T , CM000679.2:g.47946876A>T	GRCh38
NC_000017.10:g.46024242A>T , CM000679.1:g.46024242A>T	GRCh37
NC_000017.9:g.43379241A>T	NCBI36
NG_008744.1:g.10354A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225573.5:c.*94A>T	ENSP00000225573.5:n.*94A>T
ENST00000434554.7:c.*94A>T	ENSP00000399960.3:n.*94A>T
ENST00000582171.6:c.*545A>T	ENSP00000463994.1:n.*545A>T
ENST00000584806.2:n.549A>T
ENST00000641305.1:n.2379A>T
ENST00000641323.1:c.*899A>T	ENSP00000492965.1:n.*899A>T
ENST00000641427.1:n.880A>T
ENST00000641703.1:c.596A>T	ENSP00000493219.1:n.596A>T
ENST00000641709.1:c.*702A>T	ENSP00000493349.1:n.*702A>T
ENST00000641856.1:c.*1388A>T	ENSP00000493224.1:n.*1388A>T
ENST00000642017.2:c.*94A>T MANE Select	ENSP00000493302.2:n.*94A>T
ENST00000225573.4:c.*94A>T	ENSP00000225573.4:n.*94A>T
ENST00000434554.6:c.*94A>T	ENSP00000399960.2:n.*94A>T
ENST00000582171.5:c.*545A>T	ENSP00000463994.1:n.*545A>T
ENST00000584806.1:n.549A>T
NM_018129.3:c.*94A>T	NP_060599.1:n.*94A>T
XM_005257500.2:c.*94A>T	XP_005257557.1:n.*94A>T
XM_011524968.1:c.*94A>T	XP_011523270.1:n.*94A>T
XM_005257500.3:c.*94A>T	XP_005257557.1:n.*94A>T
XM_011524968.2:c.*94A>T	XP_011523270.1:n.*94A>T
XM_017024813.1:c.*94A>T	XP_016880302.1:n.*94A>T
NM_018129.4:c.*94A>T MANE Select	NP_060599.1:n.*94A>T