Canonical Allele Identifier: CA2638499484

Gene: PNPO

Linked Data

• gnomAD v4: 17-47946790-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47946790A>T , CM000679.2:g.47946790A>T	GRCh38
NC_000017.10:g.46024156A>T , CM000679.1:g.46024156A>T	GRCh37
NC_000017.9:g.43379155A>T	NCBI36
NG_008744.1:g.10268A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000225573.5:c.*8A>T	ENSP00000225573.5:n.*8A>T
ENST00000434554.7:c.*8A>T	ENSP00000399960.3:n.*8A>T
ENST00000582171.6:c.*459A>T	ENSP00000463994.1:n.*459A>T
ENST00000584806.2:n.463A>T
ENST00000641305.1:n.2293A>T
ENST00000641323.1:c.*813A>T	ENSP00000492965.1:n.*813A>T
ENST00000641427.1:n.794A>T
ENST00000641703.1:c.510A>T	ENSP00000493219.1:n.510A>T
ENST00000641709.1:c.*616A>T	ENSP00000493349.1:n.*616A>T
ENST00000641856.1:c.*1302A>T	ENSP00000493224.1:n.*1302A>T
ENST00000642017.2:c.*8A>T MANE Select	ENSP00000493302.2:n.*8A>T
ENST00000225573.4:c.*8A>T	ENSP00000225573.4:n.*8A>T
ENST00000434554.6:c.*8A>T	ENSP00000399960.2:n.*8A>T
ENST00000582171.5:c.*459A>T	ENSP00000463994.1:n.*459A>T
ENST00000584806.1:n.463A>T
NM_018129.3:c.*8A>T	NP_060599.1:n.*8A>T
XM_005257500.2:c.*8A>T	XP_005257557.1:n.*8A>T
XM_011524968.1:c.*8A>T	XP_011523270.1:n.*8A>T
XM_005257500.3:c.*8A>T	XP_005257557.1:n.*8A>T
XM_011524968.2:c.*8A>T	XP_011523270.1:n.*8A>T
XM_017024813.1:c.*8A>T	XP_016880302.1:n.*8A>T
NM_018129.4:c.*8A>T MANE Select	NP_060599.1:n.*8A>T