Canonical Allele Identifier: CA500454002

Gene: PNPO

Linked Data

• MyVariant Identifiers: chr17:g.46024058T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47946692T>C , CM000679.2:g.47946692T>C	GRCh38
NC_000017.10:g.46024058T>C , CM000679.1:g.46024058T>C	GRCh37
NC_000017.9:g.43379057T>C	NCBI36
NG_008744.1:g.10170T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225573.5:c.567T>C	ENSP00000225573.5:p.Phe189=
ENST00000434554.7:c.642T>C	ENSP00000399960.3:p.Phe214=
ENST00000582171.6:c.*361T>C	ENSP00000463994.1:n.*361T>C
ENST00000583599.6:c.456T>C	ENSP00000463919.2:p.Phe152=
ENST00000584061.6:c.627T>C	ENSP00000463972.2:p.Phe209=
ENST00000584806.2:n.365T>C
ENST00000641285.1:n.476T>C
ENST00000641305.1:n.2195T>C
ENST00000641323.1:c.*715T>C	ENSP00000492965.1:n.*715T>C
ENST00000641427.1:n.696T>C
ENST00000641511.1:c.428T>C
ENST00000641703.1:c.412T>C	ENSP00000493219.1:n.412T>C
ENST00000641709.1:c.*518T>C	ENSP00000493349.1:n.*518T>C
ENST00000641856.1:c.*1204T>C	ENSP00000493224.1:n.*1204T>C
ENST00000642017.2:c.696T>C MANE Select	ENSP00000493302.2:p.Phe232=
ENST00000225573.4:c.696T>C	ENSP00000225573.4:p.Phe232=
ENST00000434554.6:c.567T>C	ENSP00000399960.2:p.Phe189=
ENST00000582171.5:c.*361T>C	ENSP00000463994.1:n.*361T>C
ENST00000584806.1:n.365T>C
ENST00000585320.5:c.*178T>C	ENSP00000462345.1:n.*178T>C
NM_018129.3:c.696T>C	NP_060599.1:p.Phe232=
XM_005257500.2:c.456T>C	XP_005257557.1:p.Phe152=
XM_011524968.1:c.411T>C	XP_011523270.1:p.Phe137=
XM_005257500.3:c.456T>C	XP_005257557.1:p.Phe152=
XM_011524968.2:c.411T>C	XP_011523270.1:p.Phe137=
XM_017024813.1:c.456T>C	XP_016880302.1:p.Phe152=
NM_018129.4:c.696T>C MANE Select	NP_060599.1:p.Phe232=