Canonical Allele Identifier: CA1152148054
Gene: PARK7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7985317G= , CM000663.2:g.7985317G= GRCh38
NC_000001.10:g.8045377G= , CM000663.1:g.8045377G= GRCh37
NC_000001.9:g.7967964G= NCBI36
NG_008271.1:g.28664G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338639.10:c.*263G= MANE Select ENSP00000340278.5:n.*263G=
ENST00000493678.5:c.*263G= ENSP00000418770.1:n.*263G=
NM_007262.5:c.*263G= MANE Select NP_009193.2:n.*263G=
NM_001123377.2:c.*263G= NP_001116849.1:n.*263G=