Canonical Allele Identifier: CA2576858021

Gene: PNKP

Linked Data

• gnomAD v4: 19-49861579-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49861579C>G , CM000681.2:g.49861579C>G	GRCh38
NC_000019.9:g.50364836C>G , CM000681.1:g.50364836C>G	GRCh37
NC_000019.8:g.55056648C>G	NCBI36
NG_027717.1:g.10987G>C
NG_050666.1:g.17736C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000322344.8:c.1386+29G>C MANE Select	ENSP00000323511.2:n.1386+29G>C
ENST00000636840.1:c.59+29G>C
ENST00000322344.7:c.1386+29G>C	ENSP00000323511.2:n.1386+29G>C
ENST00000593946.5:c.*1313+29G>C	ENSP00000468896.1:n.*1313+29G>C
ENST00000594661.5:n.1887+29G>C
ENST00000595081.5:n.289+29G>C
ENST00000596014.5:c.1386+29G>C	ENSP00000472300.1:n.1386+29G>C
ENST00000597965.2:c.93+29G>C	ENSP00000471097.2:n.93+29G>C
ENST00000599454.5:n.306+29G>C
ENST00000600573.5:c.1293+29G>C	ENSP00000469826.1:n.1293+29G>C
ENST00000600910.5:c.1276+29G>C	ENSP00000473137.1:n.1276+29G>C
ENST00000601816.3:n.390G>C
ENST00000625216.2:c.467+29G>C	ENSP00000486898.1:n.467+29G>C
ENST00000627232.2:c.1306+29G>C	ENSP00000486037.1:n.1306+29G>C
ENST00000631020.2:c.1278+29G>C	ENSP00000486707.1:n.1278+29G>C
NM_007254.3:c.1386+29G>C	NP_009185.2:n.1386+29G>C
NM_007254.4:c.1386+29G>C MANE Select	NP_009185.2:n.1386+29G>C