Canonical Allele Identifier: CA2663093382
Gene: PNKD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218270429A>G , CM000664.2:g.218270429A>G GRCh38
NC_000002.11:g.219135152A>G , CM000664.1:g.219135152A>G GRCh37
NC_000002.10:g.218843396A>G NCBI36
NG_017060.1:g.5038A>G
NG_033036.1:g.4742T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000691799.1:n.70+709A>G
ENST00000248451.7:c.-107A>G ENSP00000248451.3:n.-107A>G
NM_001077399.2:c.-107A>G NP_001070867.1:n.-107A>G
NM_015488.4:c.-107A>G NP_056303.3:n.-107A>G