Canonical Allele Identifier: CA656368503

Gene: PNPO

Linked Data

• COSMIC: COSN21137953

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47946853_47946854insT , CM000679.2:g.47946853_47946854insT	GRCh38
NC_000017.10:g.46024219_46024220insT , CM000679.1:g.46024219_46024220insT	GRCh37
NC_000017.9:g.43379218_43379219insT	NCBI36
NG_008744.1:g.10331_10332insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225573.5:c.*71_*72insT	ENSP00000225573.5:n.*71_*72insT
ENST00000434554.7:c.*71_*72insT	ENSP00000399960.3:n.*71_*72insT
ENST00000582171.6:c.*522_*523insT	ENSP00000463994.1:n.*522_*523insT
ENST00000584806.2:n.526_527insT
ENST00000641305.1:n.2356_2357insT
ENST00000641323.1:c.*876_*877insT	ENSP00000492965.1:n.*876_*877insT
ENST00000641427.1:n.857_858insT
ENST00000641703.1:c.573_574insT	ENSP00000493219.1:n.573_574insT
ENST00000641709.1:c.*679_*680insT	ENSP00000493349.1:n.*679_*680insT
ENST00000641856.1:c.*1365_*1366insT	ENSP00000493224.1:n.*1365_*1366insT
ENST00000642017.2:c.*71_*72insT MANE Select	ENSP00000493302.2:n.*71_*72insT
ENST00000225573.4:c.*71_*72insT	ENSP00000225573.4:n.*71_*72insT
ENST00000434554.6:c.*71_*72insT	ENSP00000399960.2:n.*71_*72insT
ENST00000582171.5:c.*522_*523insT	ENSP00000463994.1:n.*522_*523insT
ENST00000584806.1:n.526_527insT
NM_018129.3:c.*71_*72insT	NP_060599.1:n.*71_*72insT
XM_005257500.2:c.*71_*72insT	XP_005257557.1:n.*71_*72insT
XM_011524968.1:c.*71_*72insT	XP_011523270.1:n.*71_*72insT
XM_005257500.3:c.*71_*72insT	XP_005257557.1:n.*71_*72insT
XM_011524968.2:c.*71_*72insT	XP_011523270.1:n.*71_*72insT
XM_017024813.1:c.*71_*72insT	XP_016880302.1:n.*71_*72insT
NM_018129.4:c.*71_*72insT MANE Select	NP_060599.1:n.*71_*72insT