Canonical Allele Identifier: CA883145045

Gene: PNKP

Linked Data

• dbSNP Id: rs1296635169
• gnomAD v3: 19-49861371-A-C
• gnomAD v4: 19-49861371-A-C
• MyVariant Identifiers: chr19:g.50364628A>C (hg19) ; chr19:g.49861371A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49861371A>C , CM000681.2:g.49861371A>C	GRCh38
NC_000019.9:g.50364628A>C , CM000681.1:g.50364628A>C	GRCh37
NC_000019.8:g.55056440A>C	NCBI36
NG_027717.1:g.11195T>G
NG_050666.1:g.17528A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322344.8:c.1449-6T>G MANE Select	ENSP00000323511.2:n.1449-6T>G
ENST00000636840.1:c.59+237T>G
ENST00000640501.1:c.55-10T>G
ENST00000322344.7:c.1449-6T>G	ENSP00000323511.2:n.1449-6T>G
ENST00000593946.5:c.*1376-6T>G	ENSP00000468896.1:n.*1376-6T>G
ENST00000594661.5:n.1950-6T>G
ENST00000595081.5:n.352-6T>G
ENST00000596014.5:c.1449-6T>G	ENSP00000472300.1:n.1449-6T>G
ENST00000597965.2:c.233T>G	ENSP00000471097.2:n.233T>G
ENST00000599454.5:n.369-6T>G
ENST00000600573.5:c.1356-6T>G	ENSP00000469826.1:n.1356-6T>G
ENST00000600910.5:c.1339-6T>G	ENSP00000473137.1:n.1339-6T>G
ENST00000601816.3:n.521-6T>G
ENST00000625216.2:c.530-6T>G	ENSP00000486898.1:n.530-6T>G
ENST00000627232.2:c.1369-6T>G	ENSP00000486037.1:n.1369-6T>G
ENST00000631020.2:c.1341-6T>G	ENSP00000486707.1:n.1341-6T>G
NM_007254.3:c.1449-6T>G	NP_009185.2:n.1449-6T>G
NM_007254.4:c.1449-6T>G MANE Select	NP_009185.2:n.1449-6T>G