Canonical Allele Identifier: CA633894434

Gene: PNKP

Linked Data

• ClinVar Variation Id: 1571497
• ClinVar RCV Id: RCV002219058
• dbSNP Id: rs770848795
• gnomAD v2: 19-50364814-AG-A
• gnomAD v4: 19-49861557-AG-A
• MyVariant Identifiers: chr19:g.50364815del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49861563del , CM000681.2:g.49861563del	GRCh38
NC_000019.9:g.50364820del , CM000681.1:g.50364820del	GRCh37
NC_000019.8:g.55056632del	NCBI36
NG_027717.1:g.11008del
NG_050666.1:g.17720del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322344.8:c.1387-48del MANE Select	ENSP00000323511.2:n.1387-48del
ENST00000636840.1:c.59+50del
ENST00000322344.7:c.1387-48del	ENSP00000323511.2:n.1387-48del
ENST00000593946.5:c.*1314-48del	ENSP00000468896.1:n.*1314-48del
ENST00000594661.5:n.1888-48del
ENST00000595081.5:n.290-48del
ENST00000596014.5:c.1387-48del	ENSP00000472300.1:n.1387-48del
ENST00000597965.2:c.94-48del	ENSP00000471097.2:n.94-48del
ENST00000599454.5:n.307-48del
ENST00000600573.5:c.1294-48del	ENSP00000469826.1:n.1294-48del
ENST00000600910.5:c.1277-48del	ENSP00000473137.1:n.1277-48del
ENST00000601816.3:n.411del
ENST00000625216.2:c.468-48del	ENSP00000486898.1:n.468-48del
ENST00000627232.2:c.1307-48del	ENSP00000486037.1:n.1307-48del
ENST00000631020.2:c.1279-48del	ENSP00000486707.1:n.1279-48del
NM_007254.3:c.1387-48del	NP_009185.2:n.1387-48del
NM_007254.4:c.1387-48del MANE Select	NP_009185.2:n.1387-48del