Canonical Allele Identifier: CA2262900728

Gene: PNPO

Linked Data

• dbSNP Id: rs2036018462
• gnomAD v4: 17-47946884-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47946884C>A , CM000679.2:g.47946884C>A	GRCh38
NC_000017.10:g.46024250C>A , CM000679.1:g.46024250C>A	GRCh37
NC_000017.9:g.43379249C>A	NCBI36
NG_008744.1:g.10362C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225573.5:c.*102C>A	ENSP00000225573.5:n.*102C>A
ENST00000434554.7:c.*102C>A	ENSP00000399960.3:n.*102C>A
ENST00000582171.6:c.*553C>A	ENSP00000463994.1:n.*553C>A
ENST00000584806.2:n.557C>A
ENST00000641305.1:n.2387C>A
ENST00000641323.1:c.*907C>A	ENSP00000492965.1:n.*907C>A
ENST00000641427.1:n.888C>A
ENST00000641703.1:c.604C>A	ENSP00000493219.1:n.604C>A
ENST00000641709.1:c.*710C>A	ENSP00000493349.1:n.*710C>A
ENST00000641856.1:c.*1396C>A	ENSP00000493224.1:n.*1396C>A
ENST00000642017.2:c.*102C>A MANE Select	ENSP00000493302.2:n.*102C>A
ENST00000225573.4:c.*102C>A	ENSP00000225573.4:n.*102C>A
ENST00000434554.6:c.*102C>A	ENSP00000399960.2:n.*102C>A
ENST00000582171.5:c.*553C>A	ENSP00000463994.1:n.*553C>A
NM_018129.3:c.*102C>A	NP_060599.1:n.*102C>A
XM_005257500.2:c.*102C>A	XP_005257557.1:n.*102C>A
XM_011524968.1:c.*102C>A	XP_011523270.1:n.*102C>A
XM_005257500.3:c.*102C>A	XP_005257557.1:n.*102C>A
XM_011524968.2:c.*102C>A	XP_011523270.1:n.*102C>A
XM_017024813.1:c.*102C>A	XP_016880302.1:n.*102C>A
NM_018129.4:c.*102C>A MANE Select	NP_060599.1:n.*102C>A