Canonical Allele Identifier: CA416489627
Gene: PINK1 HGNC NCBI
PINK1-AS HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.20974949A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.20648456A>T , CM000663.2:g.20648456A>T GRCh38
NC_000001.10:g.20974949A>T , CM000663.1:g.20974949A>T GRCh37
NC_000001.9:g.20847536A>T NCBI36
NG_008164.1:g.20002A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000321556.5:c.1124-49A>T (PINK1) MANE Select ENSP00000364204.3:n.1124-49A>T
ENST00000321556.4:c.1124-49A>T (PINK1) ENSP00000364204.3:n.1124-49A>T
ENST00000400490.2:n.217-49A>T (PINK1)
ENST00000492302.1:n.2212-49A>T (PINK1)
NM_032409.2:c.1124-49A>T (PINK1) NP_115785.1:n.1124-49A>T
NR_046507.1:n.3738T>A (PINK1-AS)
NM_032409.3:c.1124-49A>T (PINK1) MANE Select NP_115785.1:n.1124-49A>T
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Search 100 bp 3'