Canonical Allele Identifier: CA2663093807
Gene: PNKD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218270626G>T , CM000664.2:g.218270626G>T GRCh38
NC_000002.11:g.219135349G>T , CM000664.1:g.219135349G>T GRCh37
NC_000002.10:g.218843593G>T NCBI36
NG_017060.1:g.5235G>T
NG_033036.1:g.4545C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000436005.3:c.67+24G>T ENSP00000414400.3:n.67+24G>T
ENST00000472650.2:n.92+24G>T
ENST00000684905.1:n.78+24G>T
ENST00000685415.1:c.67+24G>T ENSP00000510415.1:n.67+24G>T
ENST00000687736.1:c.67+24G>T ENSP00000509627.1:n.67+24G>T
ENST00000688179.1:c.67+24G>T ENSP00000508635.1:n.67+24G>T
ENST00000689816.1:c.67+24G>T ENSP00000508450.1:n.67+24G>T
ENST00000690891.1:c.67+24G>T ENSP00000509744.1:n.67+24G>T
ENST00000691220.1:c.67+24G>T ENSP00000509580.1:n.67+24G>T
ENST00000691799.1:n.71-755G>T
ENST00000692260.1:n.82+24G>T
ENST00000273077.9:c.67+24G>T MANE Select ENSP00000273077.4:n.67+24G>T
ENST00000248451.7:c.67+24G>T ENSP00000248451.3:n.67+24G>T
ENST00000273077.8:c.67+24G>T ENSP00000273077.4:n.67+24G>T
ENST00000469689.1:n.107G>T
NM_001077399.2:c.67+24G>T NP_001070867.1:n.67+24G>T
NM_015488.4:c.67+24G>T NP_056303.3:n.67+24G>T
XM_017003771.1:c.67+24G>T XP_016859260.1:n.67+24G>T
NM_015488.5:c.67+24G>T MANE Select NP_056303.3:n.67+24G>T
NM_001077399.3:c.67+24G>T NP_001070867.1:n.67+24G>T