Canonical Allele Identifier: CA660633
Gene: PINK1 HGNC NCBI
PINK1-AS HGNC NCBI

Linked Data

dbSNP Id: rs755530256
ExAC: 1:20972008 G / A
gnomAD v2: 1-20972008-G-A
gnomAD v4: 1-20645515-G-A
MyVariant Identifiers: chr1:g.20972008G>A (hg19) chr1:g.20645515G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.20645515G>A , CM000663.2:g.20645515G>A GRCh38
NC_000001.10:g.20972008G>A , CM000663.1:g.20972008G>A GRCh37
NC_000001.9:g.20844595G>A NCBI36
NG_008164.1:g.17061G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000321556.5:c.960-45G>A (PINK1) MANE Select ENSP00000364204.3:n.960-45G>A
ENST00000321556.4:c.960-45G>A (PINK1) ENSP00000364204.3:n.960-45G>A
ENST00000400490.2:n.8G>A (PINK1)
ENST00000492302.1:n.2048-45G>A (PINK1)
NM_032409.2:c.960-45G>A (PINK1) NP_115785.1:n.960-45G>A
NR_046507.1:n.3981+70C>T (PINK1-AS)
NM_032409.3:c.960-45G>A (PINK1) MANE Select NP_115785.1:n.960-45G>A
Search 100 bp 5'
Search 100 bp 3'