Canonical Allele Identifier: CA633894441

Gene: PNKP

Linked Data

• dbSNP Id: rs1568658452
• gnomAD v2: 19-50364822-CA-C
• gnomAD v3: 19-49861565-CA-C
• gnomAD v4: 19-49861565-CA-C
• MyVariant Identifiers: chr19:g.50364823_50364824delinsG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49861566del , CM000681.2:g.49861566del	GRCh38
NC_000019.9:g.50364823del , CM000681.1:g.50364823del	GRCh37
NC_000019.8:g.55056635del	NCBI36
NG_027717.1:g.11000del
NG_050666.1:g.17723del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322344.8:c.1386+42del MANE Select	ENSP00000323511.2:n.1386+42del
ENST00000636840.1:c.59+42del
ENST00000322344.7:c.1386+42del	ENSP00000323511.2:n.1386+42del
ENST00000593946.5:c.*1313+42del	ENSP00000468896.1:n.*1313+42del
ENST00000594661.5:n.1887+42del
ENST00000595081.5:n.289+42del
ENST00000596014.5:c.1386+42del	ENSP00000472300.1:n.1386+42del
ENST00000597965.2:c.93+42del	ENSP00000471097.2:n.93+42del
ENST00000599454.5:n.306+42del
ENST00000600573.5:c.1293+42del	ENSP00000469826.1:n.1293+42del
ENST00000600910.5:c.1276+42del	ENSP00000473137.1:n.1276+42del
ENST00000601816.3:n.403del
ENST00000625216.2:c.467+42del	ENSP00000486898.1:n.467+42del
ENST00000627232.2:c.1306+42del	ENSP00000486037.1:n.1306+42del
ENST00000631020.2:c.1278+42del	ENSP00000486707.1:n.1278+42del
NM_007254.3:c.1386+42del	NP_009185.2:n.1386+42del
NM_007254.4:c.1386+42del MANE Select	NP_009185.2:n.1386+42del