Canonical Allele Identifier: CA416490015
Gene: PINK1 HGNC NCBI
PINK1-AS HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.20975110T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.20648617T>C , CM000663.2:g.20648617T>C GRCh38
NC_000001.10:g.20975110T>C , CM000663.1:g.20975110T>C GRCh37
NC_000001.9:g.20847697T>C NCBI36
NG_008164.1:g.20163T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000321556.5:c.1236T>C (PINK1) MANE Select ENSP00000364204.3:p.Cys412=
ENST00000321556.4:c.1236T>C (PINK1) ENSP00000364204.3:p.Cys412=
ENST00000400490.2:n.329T>C (PINK1)
ENST00000492302.1:n.2324T>C (PINK1)
NM_032409.2:c.1236T>C (PINK1) NP_115785.1:p.Cys412=
NR_046507.1:n.3577A>G (PINK1-AS)
NM_032409.3:c.1236T>C (PINK1) MANE Select NP_115785.1:p.Cys412=