Canonical Allele Identifier: CA2638499630

Gene: PNPO

Linked Data

• gnomAD v4: 17-47946892-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47946892C>A , CM000679.2:g.47946892C>A	GRCh38
NC_000017.10:g.46024258C>A , CM000679.1:g.46024258C>A	GRCh37
NC_000017.9:g.43379257C>A	NCBI36
NG_008744.1:g.10370C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225573.5:c.*110C>A	ENSP00000225573.5:n.*110C>A
ENST00000434554.7:c.*110C>A	ENSP00000399960.3:n.*110C>A
ENST00000582171.6:c.*561C>A	ENSP00000463994.1:n.*561C>A
ENST00000584806.2:n.565C>A
ENST00000641305.1:n.2395C>A
ENST00000641323.1:c.*915C>A	ENSP00000492965.1:n.*915C>A
ENST00000641427.1:n.896C>A
ENST00000641703.1:c.612C>A	ENSP00000493219.1:n.612C>A
ENST00000641709.1:c.*718C>A	ENSP00000493349.1:n.*718C>A
ENST00000641856.1:c.*1404C>A	ENSP00000493224.1:n.*1404C>A
ENST00000642017.2:c.*110C>A MANE Select	ENSP00000493302.2:n.*110C>A
ENST00000225573.4:c.*110C>A	ENSP00000225573.4:n.*110C>A
ENST00000434554.6:c.*110C>A	ENSP00000399960.2:n.*110C>A
ENST00000582171.5:c.*561C>A	ENSP00000463994.1:n.*561C>A
NM_018129.3:c.*110C>A	NP_060599.1:n.*110C>A
XM_005257500.2:c.*110C>A	XP_005257557.1:n.*110C>A
XM_011524968.1:c.*110C>A	XP_011523270.1:n.*110C>A
XM_005257500.3:c.*110C>A	XP_005257557.1:n.*110C>A
XM_011524968.2:c.*110C>A	XP_011523270.1:n.*110C>A
XM_017024813.1:c.*110C>A	XP_016880302.1:n.*110C>A
NM_018129.4:c.*110C>A MANE Select	NP_060599.1:n.*110C>A