Canonical Allele Identifier: CA660677
Gene: PINK1 HGNC NCBI
PINK1-AS HGNC NCBI

Linked Data

dbSNP Id: rs779637743
gnomAD v2: 1-20972153-G-T
gnomAD v4: 1-20645660-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.20645660G>T , CM000663.2:g.20645660G>T GRCh38
NC_000001.10:g.20972153G>T , CM000663.1:g.20972153G>T GRCh37
NC_000001.9:g.20844740G>T NCBI36
NG_008164.1:g.17206G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000321556.5:c.1060G>T (PINK1) MANE Select ENSP00000364204.3:p.Val354Phe
ENST00000321556.4:c.1060G>T (PINK1) ENSP00000364204.3:p.Val354Phe
ENST00000400490.2:n.153G>T (PINK1)
ENST00000492302.1:n.2148G>T (PINK1)
NM_032409.2:c.1060G>T (PINK1) NP_115785.1:p.Val354Phe
NR_046507.1:n.3906C>A (PINK1-AS)
NM_032409.3:c.1060G>T (PINK1) MANE Select NP_115785.1:p.Val354Phe