Canonical Allele Identifier: CA1328680878
Gene: PNKD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218270449A= , CM000664.2:g.218270449A= GRCh38
NC_000002.11:g.219135172A= , CM000664.1:g.219135172A= GRCh37
NC_000002.10:g.218843416A= NCBI36
NG_017060.1:g.5058A=
NG_033036.1:g.4722T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000691799.1:n.70+729A=
ENST00000248451.7:c.-87A= ENSP00000248451.3:n.-87A=
NM_001077399.2:c.-87A= NP_001070867.1:n.-87A=
NM_015488.4:c.-87A= NP_056303.3:n.-87A=