Canonical Allele Identifier: CA2638499504

Gene: PNPO

Linked Data

• gnomAD v4: 17-47946819-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47946819A>G , CM000679.2:g.47946819A>G	GRCh38
NC_000017.10:g.46024185A>G , CM000679.1:g.46024185A>G	GRCh37
NC_000017.9:g.43379184A>G	NCBI36
NG_008744.1:g.10297A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000225573.5:c.*37A>G	ENSP00000225573.5:n.*37A>G
ENST00000434554.7:c.*37A>G	ENSP00000399960.3:n.*37A>G
ENST00000582171.6:c.*488A>G	ENSP00000463994.1:n.*488A>G
ENST00000584806.2:n.492A>G
ENST00000641305.1:n.2322A>G
ENST00000641323.1:c.*842A>G	ENSP00000492965.1:n.*842A>G
ENST00000641427.1:n.823A>G
ENST00000641703.1:c.539A>G	ENSP00000493219.1:n.539A>G
ENST00000641709.1:c.*645A>G	ENSP00000493349.1:n.*645A>G
ENST00000641856.1:c.*1331A>G	ENSP00000493224.1:n.*1331A>G
ENST00000642017.2:c.*37A>G MANE Select	ENSP00000493302.2:n.*37A>G
ENST00000225573.4:c.*37A>G	ENSP00000225573.4:n.*37A>G
ENST00000434554.6:c.*37A>G	ENSP00000399960.2:n.*37A>G
ENST00000582171.5:c.*488A>G	ENSP00000463994.1:n.*488A>G
ENST00000584806.1:n.492A>G
NM_018129.3:c.*37A>G	NP_060599.1:n.*37A>G
XM_005257500.2:c.*37A>G	XP_005257557.1:n.*37A>G
XM_011524968.1:c.*37A>G	XP_011523270.1:n.*37A>G
XM_005257500.3:c.*37A>G	XP_005257557.1:n.*37A>G
XM_011524968.2:c.*37A>G	XP_011523270.1:n.*37A>G
XM_017024813.1:c.*37A>G	XP_016880302.1:n.*37A>G
NM_018129.4:c.*37A>G MANE Select	NP_060599.1:n.*37A>G