Canonical Allele Identifier: CA406932726

Gene: PNKP

Linked Data

• MyVariant Identifiers: chr19:g.50364715T>C (hg19) ; chr19:g.49861458T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49861458T>C , CM000681.2:g.49861458T>C	GRCh38
NC_000019.9:g.50364715T>C , CM000681.1:g.50364715T>C	GRCh37
NC_000019.8:g.55056527T>C	NCBI36
NG_027717.1:g.11108A>G
NG_050666.1:g.17615T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322344.8:c.1439A>G MANE Select	ENSP00000323511.2:p.Tyr480Cys
ENST00000636840.1:c.59+150A>G
ENST00000640501.1:c.45A>G
ENST00000322344.7:c.1439A>G	ENSP00000323511.2:p.Tyr480Cys
ENST00000593946.5:c.*1366A>G	ENSP00000468896.1:n.*1366A>G
ENST00000594661.5:n.1940A>G
ENST00000595081.5:n.342A>G
ENST00000596014.5:c.1439A>G	ENSP00000472300.1:p.Tyr480Cys
ENST00000597965.2:c.146A>G	ENSP00000471097.2:p.Tyr49Cys
ENST00000599454.5:n.359A>G
ENST00000600573.5:c.1346A>G	ENSP00000469826.1:p.Tyr449Cys
ENST00000600910.5:c.1329A>G	ENSP00000473137.1:p.Val443=
ENST00000601816.3:n.511A>G
ENST00000625216.2:c.520A>G	ENSP00000486898.1:n.520A>G
ENST00000627232.2:c.1359A>G	ENSP00000486037.1:n.1359A>G
ENST00000631020.2:c.1331A>G	ENSP00000486707.1:p.Tyr444Cys
NM_007254.3:c.1439A>G	NP_009185.2:p.Tyr480Cys
NM_007254.4:c.1439A>G MANE Select	NP_009185.2:p.Tyr480Cys