Canonical Allele Identifier: CA2638499480

Gene: PNPO

Linked Data

• gnomAD v4: 17-47946785-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47946785C>G , CM000679.2:g.47946785C>G	GRCh38
NC_000017.10:g.46024151C>G , CM000679.1:g.46024151C>G	GRCh37
NC_000017.9:g.43379150C>G	NCBI36
NG_008744.1:g.10263C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000225573.5:c.*3C>G	ENSP00000225573.5:n.*3C>G
ENST00000434554.7:c.*3C>G	ENSP00000399960.3:n.*3C>G
ENST00000582171.6:c.*454C>G	ENSP00000463994.1:n.*454C>G
ENST00000584061.6:c.720C>G	ENSP00000463972.2:n.720C>G
ENST00000584806.2:n.458C>G
ENST00000641305.1:n.2288C>G
ENST00000641323.1:c.*808C>G	ENSP00000492965.1:n.*808C>G
ENST00000641427.1:n.789C>G
ENST00000641703.1:c.505C>G	ENSP00000493219.1:n.505C>G
ENST00000641709.1:c.*611C>G	ENSP00000493349.1:n.*611C>G
ENST00000641856.1:c.*1297C>G	ENSP00000493224.1:n.*1297C>G
ENST00000642017.2:c.*3C>G MANE Select	ENSP00000493302.2:n.*3C>G
ENST00000225573.4:c.*3C>G	ENSP00000225573.4:n.*3C>G
ENST00000434554.6:c.*3C>G	ENSP00000399960.2:n.*3C>G
ENST00000582171.5:c.*454C>G	ENSP00000463994.1:n.*454C>G
ENST00000584806.1:n.458C>G
NM_018129.3:c.*3C>G	NP_060599.1:n.*3C>G
XM_005257500.2:c.*3C>G	XP_005257557.1:n.*3C>G
XM_011524968.1:c.*3C>G	XP_011523270.1:n.*3C>G
XM_005257500.3:c.*3C>G	XP_005257557.1:n.*3C>G
XM_011524968.2:c.*3C>G	XP_011523270.1:n.*3C>G
XM_017024813.1:c.*3C>G	XP_016880302.1:n.*3C>G
NM_018129.4:c.*3C>G MANE Select	NP_060599.1:n.*3C>G