Canonical Allele Identifier: CA2586460406

Gene: PNKP

Linked Data

• gnomAD v4: 19-49861573-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49861573G>T , CM000681.2:g.49861573G>T	GRCh38
NC_000019.9:g.50364830G>T , CM000681.1:g.50364830G>T	GRCh37
NC_000019.8:g.55056642G>T	NCBI36
NG_027717.1:g.10993C>A
NG_050666.1:g.17730G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322344.8:c.1386+35C>A MANE Select	ENSP00000323511.2:n.1386+35C>A
ENST00000636840.1:c.59+35C>A
ENST00000322344.7:c.1386+35C>A	ENSP00000323511.2:n.1386+35C>A
ENST00000593946.5:c.*1313+35C>A	ENSP00000468896.1:n.*1313+35C>A
ENST00000594661.5:n.1887+35C>A
ENST00000595081.5:n.289+35C>A
ENST00000596014.5:c.1386+35C>A	ENSP00000472300.1:n.1386+35C>A
ENST00000597965.2:c.93+35C>A	ENSP00000471097.2:n.93+35C>A
ENST00000599454.5:n.306+35C>A
ENST00000600573.5:c.1293+35C>A	ENSP00000469826.1:n.1293+35C>A
ENST00000600910.5:c.1276+35C>A	ENSP00000473137.1:n.1276+35C>A
ENST00000601816.3:n.396C>A
ENST00000625216.2:c.467+35C>A	ENSP00000486898.1:n.467+35C>A
ENST00000627232.2:c.1306+35C>A	ENSP00000486037.1:n.1306+35C>A
ENST00000631020.2:c.1278+35C>A	ENSP00000486707.1:n.1278+35C>A
NM_007254.3:c.1386+35C>A	NP_009185.2:n.1386+35C>A
NM_007254.4:c.1386+35C>A MANE Select	NP_009185.2:n.1386+35C>A