Canonical Allele Identifier: CA406932875

Gene: PNKP

Linked Data

• MyVariant Identifiers: chr19:g.50364755T>C (hg19) ; chr19:g.49861498T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49861498T>C , CM000681.2:g.49861498T>C	GRCh38
NC_000019.9:g.50364755T>C , CM000681.1:g.50364755T>C	GRCh37
NC_000019.8:g.55056567T>C	NCBI36
NG_027717.1:g.11068A>G
NG_050666.1:g.17655T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322344.8:c.1399A>G MANE Select	ENSP00000323511.2:p.Thr467Ala
ENST00000636840.1:c.59+110A>G
ENST00000640501.1:c.5A>G
ENST00000322344.7:c.1399A>G	ENSP00000323511.2:p.Thr467Ala
ENST00000593946.5:c.*1326A>G	ENSP00000468896.1:n.*1326A>G
ENST00000594661.5:n.1900A>G
ENST00000595081.5:n.302A>G
ENST00000596014.5:c.1399A>G	ENSP00000472300.1:p.Thr467Ala
ENST00000597965.2:c.106A>G	ENSP00000471097.2:p.Thr36Ala
ENST00000599454.5:n.319A>G
ENST00000600573.5:c.1306A>G	ENSP00000469826.1:p.Thr436Ala
ENST00000600910.5:c.1289A>G	ENSP00000473137.1:p.Asp430Gly
ENST00000601816.3:n.471A>G
ENST00000625216.2:c.480A>G	ENSP00000486898.1:n.480A>G
ENST00000627232.2:c.1319A>G	ENSP00000486037.1:n.1319A>G
ENST00000631020.2:c.1291A>G	ENSP00000486707.1:p.Thr431Ala
NM_007254.3:c.1399A>G	NP_009185.2:p.Thr467Ala
NM_007254.4:c.1399A>G MANE Select	NP_009185.2:p.Thr467Ala