Canonical Allele Identifier: CA400063677

Gene: PNPO

Linked Data

• MyVariant Identifiers: chr17:g.46024132A>T (hg19) ; chr17:g.47946766A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47946766A>T , CM000679.2:g.47946766A>T	GRCh38
NC_000017.10:g.46024132A>T , CM000679.1:g.46024132A>T	GRCh37
NC_000017.9:g.43379131A>T	NCBI36
NG_008744.1:g.10244A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225573.5:c.641A>T	ENSP00000225573.5:p.Glu214Val
ENST00000434554.7:c.716A>T	ENSP00000399960.3:p.Glu239Val
ENST00000582171.6:c.*435A>T	ENSP00000463994.1:n.*435A>T
ENST00000584061.6:c.701A>T	ENSP00000463972.2:p.Glu234Val
ENST00000584806.2:n.439A>T
ENST00000641305.1:n.2269A>T
ENST00000641323.1:c.*789A>T	ENSP00000492965.1:n.*789A>T
ENST00000641427.1:n.770A>T
ENST00000641703.1:c.486A>T	ENSP00000493219.1:n.486A>T
ENST00000641709.1:c.*592A>T	ENSP00000493349.1:n.*592A>T
ENST00000641856.1:c.*1278A>T	ENSP00000493224.1:n.*1278A>T
ENST00000642017.2:c.770A>T MANE Select	ENSP00000493302.2:p.Glu257Val
ENST00000225573.4:c.770A>T	ENSP00000225573.4:p.Glu257Val
ENST00000434554.6:c.641A>T	ENSP00000399960.2:p.Glu214Val
ENST00000582171.5:c.*435A>T	ENSP00000463994.1:n.*435A>T
ENST00000584806.1:n.439A>T
NM_018129.3:c.770A>T	NP_060599.1:p.Glu257Val
XM_005257500.2:c.530A>T	XP_005257557.1:p.Glu177Val
XM_011524968.1:c.485A>T	XP_011523270.1:p.Glu162Val
XM_005257500.3:c.530A>T	XP_005257557.1:p.Glu177Val
XM_011524968.2:c.485A>T	XP_011523270.1:p.Glu162Val
XM_017024813.1:c.530A>T	XP_016880302.1:p.Glu177Val
NM_018129.4:c.770A>T MANE Select	NP_060599.1:p.Glu257Val