Canonical Allele Identifier: CA539592814
Gene: PNKD HGNC NCBI

Linked Data

dbSNP Id: rs1169359484

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218270453_218270454dup , CM000664.2:g.218270453_218270454dup GRCh38
NC_000002.11:g.219135176_219135177dup , CM000664.1:g.219135176_219135177dup GRCh37
NC_000002.10:g.218843420_218843421dup NCBI36
NG_017060.1:g.5062_5063dup
NG_033036.1:g.4717_4718dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000691799.1:n.70+733_70+734dup
ENST00000248451.7:c.-83_-82dup ENSP00000248451.3:n.-83_-82dup
NM_001077399.2:c.-83_-82dup NP_001070867.1:n.-83_-82dup
NM_015488.4:c.-83_-82dup NP_056303.3:n.-83_-82dup