Canonical Allele Identifier: CA400062285

Gene: PNPO

Linked Data

• MyVariant Identifiers: chr17:g.46024013G>T (hg19) ; chr17:g.47946647G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47946647G>T , CM000679.2:g.47946647G>T	GRCh38
NC_000017.10:g.46024013G>T , CM000679.1:g.46024013G>T	GRCh37
NC_000017.9:g.43379012G>T	NCBI36
NG_008744.1:g.10125G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225573.5:c.522G>T	ENSP00000225573.5:p.Glu174Asp
ENST00000434554.7:c.597G>T	ENSP00000399960.3:p.Glu199Asp
ENST00000582171.6:c.*316G>T	ENSP00000463994.1:n.*316G>T
ENST00000583599.6:c.411G>T	ENSP00000463919.2:p.Glu137Asp
ENST00000584061.6:c.582G>T	ENSP00000463972.2:p.Glu194Asp
ENST00000584806.2:n.320G>T
ENST00000641285.1:n.431G>T
ENST00000641305.1:n.2150G>T
ENST00000641323.1:c.*670G>T	ENSP00000492965.1:n.*670G>T
ENST00000641427.1:n.651G>T
ENST00000641511.1:c.383G>T
ENST00000641703.1:c.367G>T	ENSP00000493219.1:n.367G>T
ENST00000641709.1:c.*473G>T	ENSP00000493349.1:n.*473G>T
ENST00000641856.1:c.*1159G>T	ENSP00000493224.1:n.*1159G>T
ENST00000642017.2:c.651G>T MANE Select	ENSP00000493302.2:p.Glu217Asp
ENST00000225573.4:c.651G>T	ENSP00000225573.4:p.Glu217Asp
ENST00000434554.6:c.522G>T	ENSP00000399960.2:p.Glu174Asp
ENST00000582171.5:c.*316G>T	ENSP00000463994.1:n.*316G>T
ENST00000584806.1:n.320G>T
ENST00000585320.5:c.*133G>T	ENSP00000462345.1:n.*133G>T
NM_018129.3:c.651G>T	NP_060599.1:p.Glu217Asp
XM_005257500.2:c.411G>T	XP_005257557.1:p.Glu137Asp
XM_011524968.1:c.366G>T	XP_011523270.1:p.Glu122Asp
XM_005257500.3:c.411G>T	XP_005257557.1:p.Glu137Asp
XM_011524968.2:c.366G>T	XP_011523270.1:p.Glu122Asp
XM_017024813.1:c.411G>T	XP_016880302.1:p.Glu137Asp
NM_018129.4:c.651G>T MANE Select	NP_060599.1:p.Glu217Asp