Canonical Allele Identifier: CA7709993
Gene: ALPK3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1895569
ClinVar RCV Id: RCV002574786
dbSNP Id: rs762202079
ExAC: 15:85406885 G / A
gnomAD v2: 15-85406885-G-A
gnomAD v3: 15-84863654-G-A
gnomAD v4: 15-84863654-G-A
MyVariant Identifiers: chr15:g.85406885G>A (hg19) chr15:g.84863654G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.84863654G>A , CM000677.2:g.84863654G>A GRCh38
NC_000015.9:g.85406885G>A , CM000677.1:g.85406885G>A GRCh37
NC_000015.8:g.83207889G>A NCBI36
NG_054748.1:g.52024G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000258888.6:c.4499+14G>A MANE Select ENSP00000258888.6:n.4499+14G>A
ENST00000258888.5:c.5105+14G>A ENSP00000258888.5:n.5105+14G>A
ENST00000558077.1:n.112+14G>A
NM_020778.4:c.5105+14G>A NP_065829.3:n.5105+14G>A
NM_020778.5:c.4499+14G>A MANE Select NP_065829.4:n.4499+14G>A
Search 100 bp 5'
Search 100 bp 3'