Canonical Allele Identifier: CA1147779383
Gene: PARK7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7985305C= , CM000663.2:g.7985305C= GRCh38
NC_000001.10:g.8045365C= , CM000663.1:g.8045365C= GRCh37
NC_000001.9:g.7967952C= NCBI36
NG_008271.1:g.28652C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338639.10:c.*251C= MANE Select ENSP00000340278.5:n.*251C=
ENST00000493678.5:c.*251C= ENSP00000418770.1:n.*251C=
NM_007262.5:c.*251C= MANE Select NP_009193.2:n.*251C=
NM_001123377.2:c.*251C= NP_001116849.1:n.*251C=
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