Canonical Allele Identifier: CA1152147908
Gene: PARK7 HGNC NCBI

Linked Data

dbSNP Id: rs1578107589
gnomAD v4: 1-7985171-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7985171A>G , CM000663.2:g.7985171A>G GRCh38
NC_000001.10:g.8045231A>G , CM000663.1:g.8045231A>G GRCh37
NC_000001.9:g.7967818A>G NCBI36
NG_008271.1:g.28518A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338639.10:c.*117A>G MANE Select ENSP00000340278.5:n.*117A>G
ENST00000338639.9:c.*117A>G ENSP00000340278.5:n.*117A>G
ENST00000377491.5:c.*117A>G ENSP00000366711.1:n.*117A>G
ENST00000377493.9:c.*117A>G ENSP00000466242.1:n.*117A>G
ENST00000469225.1:c.600A>G ENSP00000466756.1:n.600A>G
ENST00000493678.5:c.*117A>G ENSP00000418770.1:n.*117A>G
NM_001123377.1:c.*117A>G NP_001116849.1:n.*117A>G
NM_007262.4:c.*117A>G NP_009193.2:n.*117A>G
XM_005263424.2:c.*117A>G XP_005263481.1:n.*117A>G
XM_005263424.3:c.*117A>G XP_005263481.1:n.*117A>G
NM_007262.5:c.*117A>G MANE Select NP_009193.2:n.*117A>G
NM_001123377.2:c.*117A>G NP_001116849.1:n.*117A>G