Canonical Allele Identifier: CA2638499864

Gene: PNPO

Linked Data

• gnomAD v4: 17-47946999-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47946999G>T , CM000679.2:g.47946999G>T	GRCh38
NC_000017.10:g.46024365G>T , CM000679.1:g.46024365G>T	GRCh37
NC_000017.9:g.43379364G>T	NCBI36
NG_008744.1:g.10477G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225573.5:c.*217G>T	ENSP00000225573.5:n.*217G>T
ENST00000434554.7:c.*217G>T	ENSP00000399960.3:n.*217G>T
ENST00000582171.6:c.*668G>T	ENSP00000463994.1:n.*668G>T
ENST00000584806.2:n.672G>T
ENST00000641305.1:n.2502G>T
ENST00000641323.1:c.*1022G>T	ENSP00000492965.1:n.*1022G>T
ENST00000641427.1:n.1003G>T
ENST00000641703.1:c.719G>T	ENSP00000493219.1:n.719G>T
ENST00000641709.1:c.*825G>T	ENSP00000493349.1:n.*825G>T
ENST00000641856.1:c.*1511G>T	ENSP00000493224.1:n.*1511G>T
ENST00000642017.2:c.*217G>T MANE Select	ENSP00000493302.2:n.*217G>T
ENST00000225573.4:c.*217G>T	ENSP00000225573.4:n.*217G>T
ENST00000434554.6:c.*217G>T	ENSP00000399960.2:n.*217G>T
ENST00000582171.5:c.*668G>T	ENSP00000463994.1:n.*668G>T
NM_018129.3:c.*217G>T	NP_060599.1:n.*217G>T
XM_005257500.2:c.*217G>T	XP_005257557.1:n.*217G>T
XM_011524968.1:c.*217G>T	XP_011523270.1:n.*217G>T
XM_005257500.3:c.*217G>T	XP_005257557.1:n.*217G>T
XM_011524968.2:c.*217G>T	XP_011523270.1:n.*217G>T
XM_017024813.1:c.*217G>T	XP_016880302.1:n.*217G>T
NM_018129.4:c.*217G>T MANE Select	NP_060599.1:n.*217G>T