Canonical Allele Identifier: CA393374036
Gene: ALPK3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1776223
ClinVar RCV Id: RCV002398740
dbSNP Id: rs1476834214

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.84840276G>A , CM000677.2:g.84840276G>A GRCh38
NC_000015.9:g.85383507G>A , CM000677.1:g.85383507G>A GRCh37
NC_000015.8:g.83184511G>A NCBI36
NG_054748.1:g.28646G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000258888.6:c.997G>A MANE Select ENSP00000258888.6:p.Glu333Lys
ENST00000258888.5:c.1603G>A ENSP00000258888.5:p.Glu535Lys
NM_020778.4:c.1603G>A NP_065829.3:p.Glu535Lys
NM_020778.5:c.997G>A MANE Select NP_065829.4:p.Glu333Lys