Canonical Allele Identifier: CA406878704

Gene: PNKP

Linked Data

• MyVariant Identifiers: chr19:g.50365305T>G (hg19) ; chr19:g.49862048T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49862048T>G , CM000681.2:g.49862048T>G	GRCh38
NC_000019.9:g.50365305T>G , CM000681.1:g.50365305T>G	GRCh37
NC_000019.8:g.55057117T>G	NCBI36
NG_027717.1:g.10518A>C
NG_050666.1:g.18205T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000322344.8:c.1184A>C MANE Select	ENSP00000323511.2:p.Asn395Thr
ENST00000322344.7:c.1184A>C	ENSP00000323511.2:p.Asn395Thr
ENST00000593706.3:n.618A>C
ENST00000593946.5:c.*1111A>C	ENSP00000468896.1:n.*1111A>C
ENST00000594661.5:n.1685A>C
ENST00000596014.5:c.1184A>C	ENSP00000472300.1:p.Asn395Thr
ENST00000599454.5:n.28A>C
ENST00000600573.5:c.1091A>C	ENSP00000469826.1:p.Asn364Thr
ENST00000600910.5:c.1184A>C	ENSP00000473137.1:p.Asn395Thr
ENST00000601816.3:n.83A>C
ENST00000625216.2:c.265A>C	ENSP00000486898.1:n.265A>C
ENST00000627232.2:c.1104A>C	ENSP00000486037.1:n.1104A>C
ENST00000631020.2:c.1076A>C	ENSP00000486707.1:p.Asn359Thr
NM_007254.3:c.1184A>C	NP_009185.2:p.Asn395Thr
NM_007254.4:c.1184A>C MANE Select	NP_009185.2:p.Asn395Thr